Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP230349.RAfe5vnRc1B1gsBLrUaDHBLoOEttLqjiGli8J8p9QNUFU130_assertion description "[Based on its role in inflammatory and neurodegenerative disorders, we investigated the role of A2M and its receptor low-density lipoprotein receptor-related protein (LRP) for the development of multiple sclerosis (MS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230349.RAfe5vnRc1B1gsBLrUaDHBLoOEttLqjiGli8J8p9QNUFU130_provenance.
- NP230357.RAaeDGOFNSI4RTyF6tPcPgXpyJBvMOMRRjLGDOrQmGreU130_assertion description "[Heterozygous loss of function mutations of CASK at Xp11.4 in females cause severe intellectual disability (ID) and microcephaly with pontine and cerebellar hypoplasia (MICPCH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230357.RAaeDGOFNSI4RTyF6tPcPgXpyJBvMOMRRjLGDOrQmGreU130_provenance.
- NP230360.RAcHfs-sgqnPFoOmH5u75FcFbdaRtAU617GOKJY_mKqwc130_assertion description "[We previously showed that the preservation of neural adhesion molecule (NCAM) in differentiated thyroid carcinoma is an important indicator for a higher risk of distant metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230360.RAcHfs-sgqnPFoOmH5u75FcFbdaRtAU617GOKJY_mKqwc130_provenance.
- NP230369.RAXpwllvhgYh3PMyTHBUxj2BmiHy7_1FKMS4QW-mfcJiI130_assertion description "[Mapping of the gene that encodes the precursor protein (APP) of the β-amyloid (Aβ) present in the Aβ plaques in both AD and DS to chromosome 21 was strong evidence that this chromosome 21 gene product was a principal neuropathogenic culprit in AD as well as DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230369.RAXpwllvhgYh3PMyTHBUxj2BmiHy7_1FKMS4QW-mfcJiI130_provenance.
- NP230370.RAQgptJAHJNjGTmUnx2bvds4UGDs6nOfJW3xjWfZoV2F8130_assertion description "[Thus, array CGH resulted in an unintended predictive diagnosis of an increased tumour susceptibility as observed in Li-Fraumeni syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230370.RAQgptJAHJNjGTmUnx2bvds4UGDs6nOfJW3xjWfZoV2F8130_provenance.
- NP230373.RAVSbGZcRUE5U8G3GO4hETPduD9f8eNpISzbvjzMD88oM130_assertion description "[PEG-IFN-alfa 2b 1.5 microg/kg/wk was superior to IFN-alfa 2b in decreasing mean serum hepatitis C RNA ( P < .05 at week 12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230373.RAVSbGZcRUE5U8G3GO4hETPduD9f8eNpISzbvjzMD88oM130_provenance.
- NP230374.RAfFmy7tonqL_fdC8kMjXUsr_1t_m76ZTBJ0-mMF9VbOY130_assertion description "[CYP2C9*2 and CYP2C9*3 alleles do not influence the antihypertensive effect of losartan in men with essential hypertension and normal kidney function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230374.RAfFmy7tonqL_fdC8kMjXUsr_1t_m76ZTBJ0-mMF9VbOY130_provenance.
- NP230377.RASHVPqWqliTfxCNVGa1mzheq6mj-DFt428CzQBUa8Ofk130_assertion description "[These observations establish that p45-sErbB3 is a structurally and functionally unique gene product of ErbB3 and suggest that p45-sErbB3 is likely one of the factors involved in the osteoblastic bone metastases of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230377.RASHVPqWqliTfxCNVGa1mzheq6mj-DFt428CzQBUa8Ofk130_provenance.
- NP230390.RARKL-wzOl8ZrniDsipS3g66Z52BtDasXz05cuPl12QDE130_assertion description "[These studies strengthen the notion that HIF deregulation plays a causal role in hemangioblastoma and renal carcinoma, and raises the possibility that abnormal fibronectin matrix assembly contributes to pheochromocytoma pathogenesis in the setting of VHL disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230390.RARKL-wzOl8ZrniDsipS3g66Z52BtDasXz05cuPl12QDE130_provenance.
- NP230391.RAfEWcoKziaDuMB0ClLyvc30ubbxhCd661ykNWT2-AgpY130_assertion description "[Neither of the SNCB SNPs examined were associated with PD overall or in strata, and haplotype analyses were negative as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230391.RAfEWcoKziaDuMB0ClLyvc30ubbxhCd661ykNWT2-AgpY130_provenance.
- NP230393.RAUIqSSLQvoYBLL9XP4VrvRoMYkbZewv7XN_fUKlKX1gM130_assertion description "[We conclude that despite a markedly altered filaggrin expression in psoriatic skin, loss-of-function variants of the FLG gene are neither associated with psoriasis vulgaris nor with psoriatic arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230393.RAUIqSSLQvoYBLL9XP4VrvRoMYkbZewv7XN_fUKlKX1gM130_provenance.
- NP230394.RAc5EiDxBeBWK0AYrydhNXXTrlgVJhyWtdqulPOlspKmQ130_assertion description "[Using methylation-specific polymerase chain reaction, we analyzed the methylation status of 7 CpG islands previously identified as aberrantly methylated in pancreatic adenocarcinoma (including preproenkephalin [ppENK], p16, and thrombospondin 1) in 51 IPMNs of different histologic grades.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230394.RAc5EiDxBeBWK0AYrydhNXXTrlgVJhyWtdqulPOlspKmQ130_provenance.
- NP230401.RAfuwEuWpj6RO9VXCCxV2f587Wyn6vNhKvxa--c-IHS3o130_assertion description "[We demonstrated that HCT is effective in reducing hypercalciuria due to CLDN16 mutation on a short-term basis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230401.RAfuwEuWpj6RO9VXCCxV2f587Wyn6vNhKvxa--c-IHS3o130_provenance.
- NP230402.RAZJ2nZh4jHoWTG8voxURCS6_TtOHzubzPk9Xat8RTdZY130_assertion description "[Germline hSNF5/INI1 mutations are responsible for hereditary cases of rhabdoid tumors (RT) that constitute the rhabdoid predisposition syndrome (RPS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230402.RAZJ2nZh4jHoWTG8voxURCS6_TtOHzubzPk9Xat8RTdZY130_provenance.
- NP230403.RAR1-tLhU7bPdBczCleG1VtX3FP9T2ief6MTAA4kzgaGs130_assertion description "[Mutations in DUOX2 produce congenital hypothyroidism in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230403.RAR1-tLhU7bPdBczCleG1VtX3FP9T2ief6MTAA4kzgaGs130_provenance.
- NP230405.RAdTUOtNR-QQh6_DAeRCZzQt5PfLTAfv5ZO_Vg4JHXzOA130_assertion description "[Among these, parental stomach cancer (SIR 3.19, 95% CI 1.69-5.17) and endocrine gland tumors (SIR 3.66, 95% CI 1.32-7.17), particularly parathyroid tumors (SIR 4.46, 95% CI 1.41-9.23), were associated with offspring fibrosarcoma, and parental breast cancers with offspring leiomyosarcoma (SIR 2.04, 95% CI 1.08-3.30).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230405.RAdTUOtNR-QQh6_DAeRCZzQt5PfLTAfv5ZO_Vg4JHXzOA130_provenance.
- NP230406.RAfcRXw6LW59ubYtUeeCJk-p7vu3RdgVUUBidB5bZMW7U130_assertion description "[30 miRNAs were significantly inversely correlated with TTP whereas 28 miRNAs were significantly positively correlated with TTP of 82 cancer patients (P<0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230406.RAfcRXw6LW59ubYtUeeCJk-p7vu3RdgVUUBidB5bZMW7U130_provenance.
- NP230414.RAX1xcJZw56L9lYyFmZO-DG7IlgfREWI_27nF-r9O3XrU130_assertion description "[All selected markers except DSG3 were present at high levels in the primary tumors and at very low or non-detectable levels in normal LNs and PB in the first round of validation, indicating a potential for detecting tumor cells in NSCLC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230414.RAX1xcJZw56L9lYyFmZO-DG7IlgfREWI_27nF-r9O3XrU130_provenance.
- NP230418.RAcZAFKl_HrxzaOaEB-oW2zEJySR8qeIo1SERKAeyFJGU130_assertion description "[When compared with normal epithelium of NERD patients, (i) cathepsin D mRNA levels demonstrated a stepwise increase in expression (p<0.05) in erosive, metaplastic and EA tissue; (ii) AKR1B10 expression increased (p<0.05) 3- and 9-fold in erosive and Barrett's epithelium, respectively; and (iii) AKR1C2 levels increased (p<0.05) in erosive and Barrett's epithelium, but were reduced (p<0.05) in EA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230418.RAcZAFKl_HrxzaOaEB-oW2zEJySR8qeIo1SERKAeyFJGU130_provenance.
- NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_assertion description "[X-chromosome DNA probes for the phosphoglycerate kinase (PGK) and hypoxanthine phosphoribosyl transferase (HPRT) genes were used to study clonality in haemopoietic cells from 63 women with myeloproliferative disease, idiopathic erythrocytosis, secondary erythrocytosis or normal red cell volumes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_provenance.
- NP230427.RAdE8FyMHIgKEhHhAI6tcTDl66UrtnUKO7mNagvN-aRJA130_assertion description "[In this study, we aimed to quantify the levels of serum HBXAP DNA, to analyze and compare its diagnostic value with existing clinical parameters in lung cancer, and to potentially provide a novel tumor marker for lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230427.RAdE8FyMHIgKEhHhAI6tcTDl66UrtnUKO7mNagvN-aRJA130_provenance.
- NP230428.RAR0lWQcvSSA3u5vg6Cv6uA-nZ_KntesKCORHw-AOaCoM130_assertion description "[These findings confirm the significance of APC gene mutations in colorectal, but not oesophageal or gastric carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230428.RAR0lWQcvSSA3u5vg6Cv6uA-nZ_KntesKCORHw-AOaCoM130_provenance.
- NP230431.RAfRxE9E91jvW6OxvQcwOX_mQHfEFIu6DejVAEcmifT1A130_assertion description "[We investigated 105 consecutive AML cases for the presence of fusion gene transcripts by reverse transcriptase polymerase chain reaction (RT-PCR): AML1-ETO associated with t(8;21), CBFB-MYH11 with inv(16), PML-RARA with t(15;17), BCR-ABL with t(9;22), and MLL-AF4 with t(4;11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230431.RAfRxE9E91jvW6OxvQcwOX_mQHfEFIu6DejVAEcmifT1A130_provenance.
- NP230437.RAYBfC-hS04TLUpmBJqxLfOb5uJ8rg_62RAfBqjpK0I9c130_assertion description "[We report here on the long-term follow-up on 162 patients with high-risk chronic lymphocytic leukemia (CLL) who have undergone hematopoietic stem cell transplantation (SCT) at a single center from 1989 to 1999.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230437.RAYBfC-hS04TLUpmBJqxLfOb5uJ8rg_62RAfBqjpK0I9c130_provenance.
- NP230446.RAddG9slZPlHWzla16vTgzh70Kfp05mNO5UIxO9Xa3UHg130_assertion description "[The tumour necrosis factor receptor (TNFR)-associated periodic syndrome (TRAPS) is an autosomal dominant, multisystemic, autoinflammatory disorder caused by mutations in the TNFR1 gene ( TNFRSF1A ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230446.RAddG9slZPlHWzla16vTgzh70Kfp05mNO5UIxO9Xa3UHg130_provenance.
- NP230461.RAZCl_SqNi6gJTbbDKgczJZkMUeOXLL22fKJ_PFb7-rIs130_assertion description "[The most frequent genetic changes found so far in human malignant mesothelioma (HMM) are deletions and point mutations in the tumor suppressor genes p16INK4a and NF2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230461.RAZCl_SqNi6gJTbbDKgczJZkMUeOXLL22fKJ_PFb7-rIs130_provenance.
- NP230463.RAeuS7Sy5kdeHmFFXPtWdc4H_F7aPRSeFCrTyyBQCEAlo130_assertion description "[Novel SNPs were identified in the VDR and DBP transcription regulatory gene regions and genotyped in a case-control study using male subjects with (n=258) or without (n=434) prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230463.RAeuS7Sy5kdeHmFFXPtWdc4H_F7aPRSeFCrTyyBQCEAlo130_provenance.
- NP230464.RAfPW-S1M1yZcbkKlGAoU_uvz1ZzwHfyUYE_VXmN91XvQ130_assertion description "[Staphylococcus aureus-infected MBL null mice developed disseminated intravascular coagulation, which was associated with elevated blood IL-6 levels (but not TNF-α) and systemic inflammatory responses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230464.RAfPW-S1M1yZcbkKlGAoU_uvz1ZzwHfyUYE_VXmN91XvQ130_provenance.
- NP230467.RAdLZllUblgUjaZ9uuEPLl-9yLRnz-a7EgIaSO_YWXBKY130_assertion description "[Islet cell antibodies (ICA), autoantibodies to glutamic acid decarboxylase (GAD) and HLA genotypes were examined in 31 patients with diabetes and a mitochondrial gene mutation located at base pair 3243 (mtDNA 3243 mutation).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230467.RAdLZllUblgUjaZ9uuEPLl-9yLRnz-a7EgIaSO_YWXBKY130_provenance.
- NP230468.RAbg1rHGfu7sdhgHN2zDhD4NVvnwYQDGRyaIQdE5GC3_Y130_assertion description "[Thus, expression of Slug, Twist, MMP-2 and MMP-9 was characteristic of mesenchymal tumor areas of gliosarcomas, suggesting that mechanisms involved in the EMT in epithelial neoplasms may play roles in mesenchymal differentiation in gliosarcomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230468.RAbg1rHGfu7sdhgHN2zDhD4NVvnwYQDGRyaIQdE5GC3_Y130_provenance.
- NP230470.RAYTcnuNa3sMS6kfJS4jSEt3S5kerF4EhPBZLOO4FCG9Q130_assertion description "[We establish that some loci, notably the IBD3 and chromosome 3q linkage regions demonstrate contributions from both small intestine and colon cohorts, whereas others, notably the IBD1 (NOD2/CARD15) and IBD2 regions increase risk for small intestine or colon inflammation, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230470.RAYTcnuNa3sMS6kfJS4jSEt3S5kerF4EhPBZLOO4FCG9Q130_provenance.
- NP230472.RAUEejnsQKRIH02j1XAwvS1YLoAnc_QeXySSb3CWqfGeI130_assertion description "[Absolute OPRK1 and OXTR expression varied greatly by primary tumor type and was close to SSTR2 in small bowel NETs but not pancreatic NETs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230472.RAUEejnsQKRIH02j1XAwvS1YLoAnc_QeXySSb3CWqfGeI130_provenance.
- NP230483.RAYdO-vKUg9q9c3MhlReBKnYX8TA2PkMVkd1Az2s8vzN4130_assertion description "[Microsatellite and EGFR, HER2 and K-RAS analyses in sclerosing hemangioma of the lung.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230483.RAYdO-vKUg9q9c3MhlReBKnYX8TA2PkMVkd1Az2s8vzN4130_provenance.
- NP230486.RAbeZb93MdikgrDibAcS_IjkSRc9pxrBVuW1Job-8ulo8130_assertion description "[Rare forms of congenital hyperinsulinism (CHI) are caused by mutations in GLUD1 (encoding glutamate dehydrogenase), GCK (encoding glucokinase), HADH (encoding for L-3-hydroxyacyl-CoA dehydrogenase), SLC16A1 (encoding the monocarboxylat transporter 1), HNF4A (encoding hepatocyte nuclear factor 4α) or UCP2 (encoding mitochondrial uncoupling protein 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230486.RAbeZb93MdikgrDibAcS_IjkSRc9pxrBVuW1Job-8ulo8130_provenance.
- NP230497.RATdLADuwHbNCmAoG5ABpn1NP_67d_HKw1D6mBsLuUG3c130_assertion description "[Our data also indicate that somatic FH mutations appear to be limited to tumor types observed in hereditary leiomyomatosis and renal cell cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230497.RATdLADuwHbNCmAoG5ABpn1NP_67d_HKw1D6mBsLuUG3c130_provenance.
- NP230499.RAXDRhFeO2Cm9J-MwCK2EMNcOWXEpj8Z6dPVu0DWg82Us130_assertion description "[Results IGHV genes derived from major subgroups 1, 3, 4 and 5 and a diverse set of IGHD and IGHJ genes were shown to create the IgE repertoire in patients diagnosed with NAFES and CRS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230499.RAXDRhFeO2Cm9J-MwCK2EMNcOWXEpj8Z6dPVu0DWg82Us130_provenance.
- NP230504.RAd-_tLRdHWclZBWJYBU9Qoo-ZtIrn6RnhX9mUfcnMpPg130_assertion description "[The most common presenting sign of retinoblastoma is leukocoria; the second most common presenting sign is strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230504.RAd-_tLRdHWclZBWJYBU9Qoo-ZtIrn6RnhX9mUfcnMpPg130_provenance.
- NP230507.RAS8EZArfRtbfO5UQv1ro8WHaUklTstkFltrykSwxfrbQ130_assertion description "[The gene that encodes hepcidin expression (HAMP) is subject to regulation by proinflammatory cytokines, such as IL-6 and IL-1; excessive hepcidin production explains the relative deficiency of iron during inflammatory states, eventually resulting in the anaemia of inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230507.RAS8EZArfRtbfO5UQv1ro8WHaUklTstkFltrykSwxfrbQ130_provenance.
- NP230508.RAZEoxwoi78G2NWg3xhEMQfmUVJhAx_NCwk6WIzGP9Sgk130_assertion description "[Ezrin phosphorylation and translocation are thought to be correlated with cell motility, invasion, and carcinoma metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230508.RAZEoxwoi78G2NWg3xhEMQfmUVJhAx_NCwk6WIzGP9Sgk130_provenance.
- NP230510.RAccmSvC3BBeUqdx0CWTGR7ERfmscfKXlajiabkacyL7M130_assertion description "[The reduced DMPK and the delayed slow fiber maturation in congenital DM1 may be two separate consequences of nuclear retention of DMPK RNA transcripts with expanded CUG repeats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230510.RAccmSvC3BBeUqdx0CWTGR7ERfmscfKXlajiabkacyL7M130_provenance.
- NP230519.RAQvTLEzuNxdODWd0GqT40scVFaRnFGL8X59_wxqoTMiY130_assertion description "[In addition, we found that the level of MTA1 protein was progressively up-regulated, whereas that of miR-661 and its activator, c/EBPalpha, were down-regulated in a breast cancer progression model consisting of MCF-10A cell lines whose phenotypes ranged from noninvasive to highly invasive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230519.RAQvTLEzuNxdODWd0GqT40scVFaRnFGL8X59_wxqoTMiY130_provenance.
- NP230529.RASyVGSswTxwoNnPpADfv45JIq4NhE_rKxU-D8ZJPTO-w130_assertion description "[Coincidentally, RFC40 is overexpressed in gestational trophoblastic diseases such as choriocarcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230529.RASyVGSswTxwoNnPpADfv45JIq4NhE_rKxU-D8ZJPTO-w130_provenance.
- NP230533.RARI9QlJkLs7xvlRUsSJlLczWtnwYCUBeOePTpglVRS6Q130_assertion description "[A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230533.RARI9QlJkLs7xvlRUsSJlLczWtnwYCUBeOePTpglVRS6Q130_provenance.
- NP230539.RAYpQMNOM1o0YKILxXQtgHat_QmwTbaFjHa_maEU8duKA130_assertion description "[During acute HIV infection (AHI), detection depends on assay sensitivity for p24 Ag.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230539.RAYpQMNOM1o0YKILxXQtgHat_QmwTbaFjHa_maEU8duKA130_provenance.
- NP230548.RAbSvHANPnSPS46IWsyqhYli4TtFmQByLiZMKGepF5XNo130_assertion description "[The role of heme oxygenase-1 in pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230548.RAbSvHANPnSPS46IWsyqhYli4TtFmQByLiZMKGepF5XNo130_provenance.
- NP230552.RAYgl0b_qXs3de7mE9CwJ7_QNUETxQw3vvAVVC3MSHq-s130_assertion description "[RFC methylation is more common in PCNSL compared with systemic DLBCL, and is associated with a lower CR rate to HD-MTX-based chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230552.RAYgl0b_qXs3de7mE9CwJ7_QNUETxQw3vvAVVC3MSHq-s130_provenance.
- NP230554.RAW8K4Y-tggux7vft8Oe9szyhulB4cX_T1Kd1-m10lUqs130_assertion description "[In Middle and Northern Europe the frequency of G6PD is much lower, and with approximately 0.0005, comparable with the frequency of pyruvate kinase (PK) enzymopathies, the most frequent enzyme deficiency in glycolysis in this area (Luzzatto, 1987; Beutler and Kuhl, 1990).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230554.RAW8K4Y-tggux7vft8Oe9szyhulB4cX_T1Kd1-m10lUqs130_provenance.
- NP230559.RAUTg64TcCZ8I6mZ7Ef8uI22Nslc6OHK6P99yG9VOuDbk130_assertion description "[Bone marrow-derived primitive CD34(+) and CD33(+)/CD34(-) progenitor cells from SCN patients evolving to AML, all with mutations in the granulocyte colony-stimulating factor receptor (G-CSFR) gene, demonstrated normal cell survival, whereas more differentiated CD15(+)/CD33(-)/CD34(-) cells negative for mutant G-CSFR gene, continue to exhibit accelerated apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230559.RAUTg64TcCZ8I6mZ7Ef8uI22Nslc6OHK6P99yG9VOuDbk130_provenance.
- NP230565.RAVnA44XFLTafBvjcvSdq_DFCEDdJYd4Z53rdxVKiGtFk130_assertion description "[The application of IgM EIA is especially important in cases of meningitis when CSF samples are not available and for diagnosis of enterovirus diseases with other clinical symptoms such as fever, enteritis, and hand-foot-and-mouth disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230565.RAVnA44XFLTafBvjcvSdq_DFCEDdJYd4Z53rdxVKiGtFk130_provenance.
- NP230568.RAc3vuHczZQdTErq2raTmaLDNCl1GulyFy53UdcBL5e2Y130_assertion description "[A comparative study of the efficacy of simvastatin and gemfibrozil in combined hyperlipoproteinemia: prediction of response by baseline lipids, apo E genotype, lipoprotein(a) and insulin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230568.RAc3vuHczZQdTErq2raTmaLDNCl1GulyFy53UdcBL5e2Y130_provenance.
- NP230574.RARKxTxZPBWwERc7qNVSDYseZnG7JiJkBWAQOhKEtxMqk130_assertion description "[A microdeletion of the HBII-85 snoRNAs in a child with PWS provides, in combination with previous data, effectively conclusive evidence that deficiency of HBII-85 snoRNAs causes the key characteristics of the PWS phenotype, although some atypical features suggest that other genes in the region may make more subtle phenotypic contributions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230574.RARKxTxZPBWwERc7qNVSDYseZnG7JiJkBWAQOhKEtxMqk130_provenance.
- NP230575.RAZQpH9ghsK6yS6-DaCD_YbWU4GCAGMVdEVlvLIdhxe-k130_assertion description "[Because 4 geriatric patients (aged 67-94) were found to have the rate c-mos allele (A2), and the frequency of this A2 allele was no higher among the lymphoma/leukemia patients than among cancer-free individuals, it is unlikely that it constitutes a marker for NHL or ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230575.RAZQpH9ghsK6yS6-DaCD_YbWU4GCAGMVdEVlvLIdhxe-k130_provenance.
- NP230589.RAfy0sWjt14wtrEW8hFXVIOxlILghCOWKctL3o2KTdiTk130_assertion description "[Among participants who had all three suspected aflatoxin-related high-risk genotypes [GSTM1 null, HLY1*2 (HY/HH), and XRCC1 (AG/GG)], a significant 15-fold increased risk of HCC was observed albeit with imprecise estimates (OR, 14.7; 95% CI, 1.27-169).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230589.RAfy0sWjt14wtrEW8hFXVIOxlILghCOWKctL3o2KTdiTk130_provenance.
- NP230592.RAS8p2DryIuAueBHCxfEic80QcdlDIk3-7rbBENYo0J-Y130_assertion description "[The BTNL2 rs2076530 polymorphism is associated with T1D, RA, and SLE because of its strong linkage disequalibrium with predisposing HLA DQB1-DRB1 haplotypes in Caucasian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230592.RAS8p2DryIuAueBHCxfEic80QcdlDIk3-7rbBENYo0J-Y130_provenance.
- NP230595.RAeJCZkKfqv8mxSaPMMJ6vUqIj9geq_1K3MDQlQpaCCAo130_assertion description "[A new subtype of pre-B acute lymphoblastic leukemia with t(5;12)(q31q33;p12), molecularly and cytogenetically distinct from t(5;12) in chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230595.RAeJCZkKfqv8mxSaPMMJ6vUqIj9geq_1K3MDQlQpaCCAo130_provenance.
- NP230601.RAUb-FpjJxCKypoNeuaeUY2abG8TLtIGfuFXHudVuYw8o130_assertion description "[Average MKP1/DUSP1 mRNA expression was increased by 8.2-fold (SEM, +/-2.9) following dexamethasone versus 1.1-fold (SEM, +/-0.4) following normal saline (P = 0.009).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230601.RAUb-FpjJxCKypoNeuaeUY2abG8TLtIGfuFXHudVuYw8o130_provenance.
- NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_assertion description "[To investigate whether the PRND polymorphisms are associated with an increased risk for developing sporadic CJD in the Korean population, we compared the genotype and allele frequencies of PRND polymorphisms in 110 sporadic CJD patients with those in 102 healthy Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230602.RAYA-eaLRWxt3Uesd33ivmMGUsfAyywdr7TBIM-3Ivg4k130_provenance.
- NP230616.RAaTc4JvJhw0VAvanyJQNwH9zWFTClVACHLn6uUcY-_Mk130_assertion description "[Differentiation from neuroblastoma may be made based on immunoreactivity for beta 2 microglobulin and HBA71 and lack of immunoreactivity for chromogranin in PPNET and MSCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230616.RAaTc4JvJhw0VAvanyJQNwH9zWFTClVACHLn6uUcY-_Mk130_provenance.
- NP230623.RAUU7HU_rGCuoZsmSgjqpvuqol-JagLe67yyAhOXFvDbA130_assertion description "[In particular, a strong association has been found between SF3B1 mutation and refractory anemia with ring sideroblasts, a condition characterized by ineffective erythropoiesis and parenchymal iron overload.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230623.RAUU7HU_rGCuoZsmSgjqpvuqol-JagLe67yyAhOXFvDbA130_provenance.
- NP230626.RAYvcG87Fn478QUMuXrpzZKgTc7PuUfIGAQSZpoEyqPJY130_assertion description "[In this immunohistochemical study, we showed recruitment of ataxin-2, ataxin-3 and TATA box binding protein (TBP) into NIIs of the pontine neurons of spinocerebellar ataxia type (SCA) 1, SCA2, SCA3 and dentatorubral-pallidoluysian atrophy brains.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230626.RAYvcG87Fn478QUMuXrpzZKgTc7PuUfIGAQSZpoEyqPJY130_provenance.
- NP230630.RARFDf6c3CsYGSaO2SDtLaTyXA-BYpqZmvO1ps4MkbmCQ130_assertion description "[The Xpert MTB/RIF test enables rapid detection of tuberculosis (TB) and rifampicin resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230630.RARFDf6c3CsYGSaO2SDtLaTyXA-BYpqZmvO1ps4MkbmCQ130_provenance.
- NP230633.RAU_CcBQwH6jsXHZIrAi4IF0dzSXC3-9kvQCsB6Q2Bk9Q130_assertion description "[The neoplasms, respectively, did not show germline SDHA, SDHB, SDHC, and SDHD, and KIT mutations associated with familial paraganglioma and familial GIST.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230633.RAU_CcBQwH6jsXHZIrAi4IF0dzSXC3-9kvQCsB6Q2Bk9Q130_provenance.
- NP230641.RAS9JJrVu8KeT-m3EVNhU4UGI2X3XhSqCcdPqeLh-g09M130_assertion description "[These data demonstrate that i) increased flux of cholesterol from HDL into the liver via SR-BI as a result of phospholipase modification of the HDL particle translates neither into increased biliary and fecal sterol output nor into increased gallstone formation, and ii) increased sPLA2 expression in patients with cholesterol gallstones might be a consequence rather than the underlying cause of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230641.RAS9JJrVu8KeT-m3EVNhU4UGI2X3XhSqCcdPqeLh-g09M130_provenance.
- NP230642.RAaa6HS7RLIppFDXKR95LRsKq3V0Q3yoHJTGGNLYrQYMg130_assertion description "[Furthermore, although neither the prevalence nor the concentration of total anti-MSP-1(19) antibodies was associated with resistance to malaria in African children, significant associations were observed between antibody fine specificity and subsequent risk of infection and high-density parasitemia during a follow-up period.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230642.RAaa6HS7RLIppFDXKR95LRsKq3V0Q3yoHJTGGNLYrQYMg130_provenance.
- NP230647.RAfqjgvqAiEL00XN9e_Du_vC0VFys-orNklGL2n8Em62w130_assertion description "[A strong Bcl-2 expression was found in the four cases of Brca2 -associated carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230647.RAfqjgvqAiEL00XN9e_Du_vC0VFys-orNklGL2n8Em62w130_provenance.
- NP230654.RAbeFEE7_nqk7dPkq1high63DT6a_c1yKMUR02xc82KHU130_assertion description "[Although associations have been reported for various cancers, this paper focuses on urinary bladder cancer, a cancer in which a role for NAT2 polymorphism was first proposed and for which evidence is accumulating that the effect is biologically significant with important public health implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230654.RAbeFEE7_nqk7dPkq1high63DT6a_c1yKMUR02xc82KHU130_provenance.
- NP230656.RASj4U2YTzo-SKVdGDFAqkVOYv-oqEHOJXWWPmGbV72cA130_assertion description "[The upregulated MT1-MMP expression in type 1 diabetes may be the result of higher maternal insulin and TNF-alpha levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230656.RASj4U2YTzo-SKVdGDFAqkVOYv-oqEHOJXWWPmGbV72cA130_provenance.
- NP230657.RAav_ASzFRKfobIbCWDdgbBP_uTKts9hi5DFVzRucw9iU130_assertion description "[In order to see if these families had mutations in the SLC4A11 gene, we selected 11 microsatellite markers from the CHED2 candidate region and used them to genotype the families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230657.RAav_ASzFRKfobIbCWDdgbBP_uTKts9hi5DFVzRucw9iU130_provenance.
- NP230658.RASmb5DhZtgtkeUAMFBj2bcxobE-S6lzMpMsZLYESembM130_assertion description "[This study sought to define the genetic architecture of ADIPOQ in the comprehensively phenotyped Hispanic (n = 1,151) and African American (n = 574) participants from the Insulin Resistance Atherosclerosis Family Study (IRASFS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230658.RASmb5DhZtgtkeUAMFBj2bcxobE-S6lzMpMsZLYESembM130_provenance.
- NP230663.RAZ8E34y3JONcrrpLAaWqJYnzuzpdTmrAdpMnksEXuqBk130_assertion description "[TMPRSS2 exon 1 was fused in-frame with ERG exon 4 in 17 of 34 (50%) prostate carcinomas and in 4 of 19 (21%) HGPIN lesions, but in none of controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230663.RAZ8E34y3JONcrrpLAaWqJYnzuzpdTmrAdpMnksEXuqBk130_provenance.
- NP230668.RAbVxPqkrAM7NDw_Ym94xJW3oNED02ui93MUMyGcvUGGM130_assertion description "[The effects of VDR gene polymorphisms including immunomodulation, stimulation of cellular differentiation and inhibition of proliferation make it a possible candidate for therapy of psoriasis as well as for the psoriasis gene modification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230668.RAbVxPqkrAM7NDw_Ym94xJW3oNED02ui93MUMyGcvUGGM130_provenance.
- NP230670.RARZJ20uKI4yfXeuGtQhJJvsRLfc_3ZJ6HsonTff-MnPc130_assertion description "[Studies performed with ADPKD cyst-lining epithelial cells (CC) by comparison with normal tubular cells indicate that integrin alpha(6)beta(4)-Ln-5 interactions are involved in cellular events of potential importance for cystogenesis: 1) laminin 5 is a preferential adhesion substrate for CC, mainly through alpha(6)beta(4) interaction, 2) CC increased haptotactic and chemotactic motility depends on the presence of Ln-5 and requires integrin alpha(3)beta(1) cooperation, and 3) CC haptotactic or chemotactic migration is specifically increased by mAb-mediated beta(4) integrin ligation, through an alpha(3)beta(1) integrin-dependent and independent pathway, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230670.RARZJ20uKI4yfXeuGtQhJJvsRLfc_3ZJ6HsonTff-MnPc130_provenance.
- NP230674.RAWXFzBYchB7Bbobre1mevuNZa5PghoB2meC_gn-uvFG4130_assertion description "[Coordinated reduction of genes of oxidative metabolism in humans with insulin resistance and diabetes: Potential role of PGC1 and NRF1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230674.RAWXFzBYchB7Bbobre1mevuNZa5PghoB2meC_gn-uvFG4130_provenance.
- NP230677.RAbsBAIHYnQ6VSxPlna1wixG_TYmpXVs5GQ-Wh1utoazY130_assertion description "[It is worthy to note that the significant downregulation of full-length MDM4 in PTC reveals a novel status of this factor in human cancer that counsels careful evaluation of its role in human tumorigenesis and of its potential as therapeutic target.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230677.RAbsBAIHYnQ6VSxPlna1wixG_TYmpXVs5GQ-Wh1utoazY130_provenance.
- NP230681.RAXdAEijy7tXwi3SEGHhmtyvx9HPUKUYu5RL4J8FlxclY130_assertion description "[Recent studies showed that dominant negative mutations in the insulin promoter factor-1 (IPF-1), a pancreatic beta-cell specific transcription factor, cause maturity-onset diabetes of the young (MODY), a subtype of T2DM with early onset and monogenic autosomal inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230681.RAXdAEijy7tXwi3SEGHhmtyvx9HPUKUYu5RL4J8FlxclY130_provenance.
- NP230691.RAexBLP6OksH5X5_Qvz_muF3CgDn_pRpmjP5CAiSAjx9s130_assertion description "[DRD2 and DRD4 in relation to regular alcohol and cannabis use among adolescents: does parenting modify the impact of genetic vulnerability? The TRAILS study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230691.RAexBLP6OksH5X5_Qvz_muF3CgDn_pRpmjP5CAiSAjx9s130_provenance.
- NP230692.RAXOjAcowUelMv6sV1RYHnQTJ7u4RKZ7XUyGNqVnhWpbs130_assertion description "[This study investigated whether the prolonged survival of inflammatory cells in periodontal disease could be due to the inhibition of apoptosis by tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) decoy receptors and inhibition of the terminal stages of apoptosis signaling by inhibitor of apoptosis (IAP) family members.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230692.RAXOjAcowUelMv6sV1RYHnQTJ7u4RKZ7XUyGNqVnhWpbs130_provenance.
- NP230693.RAauojqRm0H2ca6v1F3lE9M2Mzm_-0UpSpY_7qUPcmtiA130_assertion description "[To our knowledge this is the first report that describes an intrinsic molecular change, namely methylation of the p16 gene CpG island, common to all three histological patterns associated with Cushing's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230693.RAauojqRm0H2ca6v1F3lE9M2Mzm_-0UpSpY_7qUPcmtiA130_provenance.
- NP230697.RAZhXuVYKrEN9Gx7BaAuTAH3aFxLwFGfP44ts7P6oP3v4130_assertion description "[These findings suggest a role for u-PA and PAI-1 in a relatively early stage of melanoma metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230697.RAZhXuVYKrEN9Gx7BaAuTAH3aFxLwFGfP44ts7P6oP3v4130_provenance.
- NP230699.RAdiX9cLX9JV62APSf-885K3iOZB67mKVrASMTChb5VMg130_assertion description "[Genetic variants in CASP3, BMP5, and IRS2 genes may influence survival in prostate cancer patients receiving androgen-deprivation therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230699.RAdiX9cLX9JV62APSf-885K3iOZB67mKVrASMTChb5VMg130_provenance.
- NP230704.RAUhbhrtAx6JBjHiTrTNfd223xfP-ZcK1FVFeZuN869b8130_assertion description "[Several studies have associated a polymorphism (SNP309 T/G) in the promoter region of MDM2 with higher levels of this protein, which will favor p53-pathway abolishment, cell-cycle escape, and development of cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230704.RAUhbhrtAx6JBjHiTrTNfd223xfP-ZcK1FVFeZuN869b8130_provenance.
- NP230707.RATl_tB5QO3TTn57JhX9vEAUd6ua-UDxM3ppBMxmVGvMY130_assertion description "[In addition, the overexpression of VEGF had no effect on the ability of LM7/Fas cells to form lung metastases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230707.RATl_tB5QO3TTn57JhX9vEAUd6ua-UDxM3ppBMxmVGvMY130_provenance.
- NP230708.RAdF8GkF3hjAp3jkN_r7PFOcf1B9FhIa4MkKu6aEzwgck130_assertion description "[Of the paired samples, lymph nodes (93% consistency) and visceral metastases (96% consistency) presented a highly similar distribution of BRAF/NRAS mutations versus primary melanomas, with a significantly less consistent pattern in brain (80%) and skin metastases (75%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230708.RAdF8GkF3hjAp3jkN_r7PFOcf1B9FhIa4MkKu6aEzwgck130_provenance.
- NP230722.RASzZFA7OPJ7ARh7xCOf5W-L3Q1ulv8YyKpH5a5n4PTyM130_assertion description "[Since tumor protein D52 (TPD52) has been identified as a chromosome 8q21 amplification target in breast and prostate carcinoma, we compared TPD52 expression in normal ovarian epithelium (n = 9), benign serous adenomas (n = 11), serous borderline tumors (n = 6) and invasive carcinomas of the major histologic subtypes (n = 57) using immunohistochemistry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230722.RASzZFA7OPJ7ARh7xCOf5W-L3Q1ulv8YyKpH5a5n4PTyM130_provenance.
- NP230723.RAXGjPzkPtDAK9Y-Jf1NbYGHoSggw4E2zM_WUX6HpUjTw130_assertion description "[Dominance of CD4+ lymphocytic infiltrates with disturbed effector cell characteristics in the tumor microenvironment of prostate carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230723.RAXGjPzkPtDAK9Y-Jf1NbYGHoSggw4E2zM_WUX6HpUjTw130_provenance.
- NP230724.RAUPsKWrfBotujEY_ROzRFT4BzImlHf-_AEDophnIyavk130_assertion description "[RFALS is clinically and genetically heterogeneous and the locus of RFALS type 3 was mapped to 2q33 (ALS2) in a single family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230724.RAUPsKWrfBotujEY_ROzRFT4BzImlHf-_AEDophnIyavk130_provenance.
- NP230728.RAT7ZCQ0UQSad3ssZQvW7SFiNKXM3jr8GVmCS1JBqbrv0130_assertion description "[The novel findings of this study that warrant replication are the evidence for interaction of coffee with APOE, and of smoking with REP1 on PD risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230728.RAT7ZCQ0UQSad3ssZQvW7SFiNKXM3jr8GVmCS1JBqbrv0130_provenance.
- NP230730.RAWvguAckeEZQ_-SCkOkGeyECXqhkd7fcdRsn1y6QNwy8130_assertion description "[Genetic disorders of excessive salt loss from sweat glands have been observed in pseudohypoaldosteronism type I (PHA) and cystic fibrosis that result from mutations in genes encoding epithelial Na+ channel (ENaC) subunits and the transmembrane conductance regulator (CFTR), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230730.RAWvguAckeEZQ_-SCkOkGeyECXqhkd7fcdRsn1y6QNwy8130_provenance.
- NP230732.RASL9sW6xanYUOAna1a6CY61ZnqV-aOFyDw5BOgP8AiHc130_assertion description "[Reduced CXCL12/CXCR4 results in impaired learning and is downregulated in a mouse model of Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230732.RASL9sW6xanYUOAna1a6CY61ZnqV-aOFyDw5BOgP8AiHc130_provenance.
- NP230754.RARU1m0X9msL1a5hKg8-8ZKi9yGq3fiEIo9lDzkgoXFt8130_assertion description "[We describe three individuals from two families with a recessive inborn error of metabolism, characterized by megaloblastic anemia and/or pancytopenia, severe cerebral folate deficiency, and cerebral tetrahydrobiopterin deficiency due to a germline missense mutation in DHFR, resulting in profound enzyme deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230754.RARU1m0X9msL1a5hKg8-8ZKi9yGq3fiEIo9lDzkgoXFt8130_provenance.
- NP230759.RAbtPVvC_4Nk6d6rRPqanEEFsEEzLLRVUDj2O7vydSwCo130_assertion description "[Although the function of bFGF in normal cells remains unknown, its production in neoplastic conditions may be responsible for the associated desmoplastic and angioblastic proliferations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230759.RAbtPVvC_4Nk6d6rRPqanEEFsEEzLLRVUDj2O7vydSwCo130_provenance.
- NP230763.RAXaeEHIMfWlbV7gSQLH2T3hWRhMtL7FqEbR7Y9yPD5bY130_assertion description "[Molecular screening of 7 genes (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2, KCNJ2, CAV3) associated with LQTS was performed with denaturing high-performance liquid chromatography and nucleotide sequencing of genomic DNA from 201 cases diagnosed as SIDS according to the Nordic Criteria, and from 182 infant and adult controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230763.RAXaeEHIMfWlbV7gSQLH2T3hWRhMtL7FqEbR7Y9yPD5bY130_provenance.
- NP230769.RATgovVCl2UwMIl3ha2GfOY7SelGjHrWMWYAgwRVexOLg130_assertion description "[Extra domain-B containing fibronectin (EDB(+) FN), a recently proposed marker of angiogenesis, has been shown to be expressed in a number of human cancers and in ocular neovascularization in patients with proliferative diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230769.RATgovVCl2UwMIl3ha2GfOY7SelGjHrWMWYAgwRVexOLg130_provenance.
- NP230773.RAbZZTdVz7VjRepQYpGLDfcNXJeyvSO28XgrTE1ULQKQI130_assertion description "[The question of whether cancer stem/tumor-initiating cells (CSC/TIC) exist in human melanomas has arisen in the last few years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230773.RAbZZTdVz7VjRepQYpGLDfcNXJeyvSO28XgrTE1ULQKQI130_provenance.
- NP230777.RARdYa1sjVK5y02fYeakdQpp5XkbPcHJepX-K7Ts6lE6U130_assertion description "[We conclude that the rate of the predominant Jewish BRCA1 and BRCA2 mutations in CaP patients does not significantly differ from that of the general population, and that mutational inactivation of the BRCA1 is rare in familial CaP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230777.RARdYa1sjVK5y02fYeakdQpp5XkbPcHJepX-K7Ts6lE6U130_provenance.
- NP230779.RAWh_AdrOS-Zerj-TyeaAeolWX1gxVIgM4sgly8q8D5E8130_assertion description "[Although genetic variants in ICAM5 showed the strongest association with disease status, ICAM1 is expressed at highest levels in normal and tumor breast tissue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230779.RAWh_AdrOS-Zerj-TyeaAeolWX1gxVIgM4sgly8q8D5E8130_provenance.
- NP230782.RAZMYhnwBcMTWQrk9ozMf1eD_G2GTb-T7hzKkK503XMRg130_assertion description "[Chaudhary and colleagues observed associations of matrix metalloproteinase (MMP)-2 (-1306C/T) and MMP-9 (-1562C/T) promoter polymorphisms with head and neck squamous cell carcinoma (HNSCC), but not with oral submucous fibrosis (OSMF) in an Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230782.RAZMYhnwBcMTWQrk9ozMf1eD_G2GTb-T7hzKkK503XMRg130_provenance.
- NP230783.RAViW8mTf2q9h6DXAhgFy3CVjABJHuT62h9CWApD6W1TQ130_assertion description "[Thus, T-cell targeting by CD3xCD19 bispecific and CD28 antibodies may be used to eliminate leukemic B cells ex vivo and reconstitute immunological control of residual malignant disease by the induction of anti-tumoral T-cell responses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230783.RAViW8mTf2q9h6DXAhgFy3CVjABJHuT62h9CWApD6W1TQ130_provenance.
- NP230784.RAU2CZLhTlcZ9EOSfyGlMlUSw5339lj8g89KUVVaHtmgk130_assertion description "[A variant (rs8090011) in the LAMA1 gene was associated with type 2 diabetes in lean cases (P = 8.4×10⁻⁹, OR = 1.13 [95% CI 1.09-1.18]), and this association was stronger than that in obese cases (P = 0.04, OR = 1.03 [95% CI 1.00-1.06]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230784.RAU2CZLhTlcZ9EOSfyGlMlUSw5339lj8g89KUVVaHtmgk130_provenance.
- NP230791.RAdwTAlKtMvJ32N0ZQc8YwUjx32GM0bH8i34eIfv7cvRE130_assertion description "[Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230791.RAdwTAlKtMvJ32N0ZQc8YwUjx32GM0bH8i34eIfv7cvRE130_provenance.