Nanopublications

Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }

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NP217629.RAnLQSEDzOaYW61dQsjC9bATVLOBX3otnjXMQfSvNMbDs130_assertion description "[Malaria is globally endemic in tropical and subtropical regions and so is the hemoglobinopathies, thalassemias and glucose-6-phosphate dehydrogenase (G6PD) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217629.RAnLQSEDzOaYW61dQsjC9bATVLOBX3otnjXMQfSvNMbDs130_provenance.
NP217635.RAgUvj-vf74L5hUqs1VBVtsyWsk2KLo1UPHut7szIh194130_assertion description "[Recently, an association of a single nucleotide polymorphism, 163A>G encoding M55V, in the gene SUMO4, which has been shown to be a negative feedback regulator for nuclear factor kappaB, has been reported in type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217635.RAgUvj-vf74L5hUqs1VBVtsyWsk2KLo1UPHut7szIh194130_provenance.
NP217639.RAjp2G7DoljtHcTwEU5xy7P40nEmFFdJjzHeQvXdRRDGE130_assertion description "[To investigate whether the killer cell immunoglobulin-like receptor (KIR) gene polymorphism and the corresponding specific HLA ligands in parent couples possessing a susceptibility to unexplained recurrent spontaneous abortion (RSA), we searched 73 pairs of childless couples with three or more abortions characterized as unexplained RSA and 68 pairs of healthy control couples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217639.RAjp2G7DoljtHcTwEU5xy7P40nEmFFdJjzHeQvXdRRDGE130_provenance.
NP217640.RAt3G0BNm1xdwR5k8xzxaGgSiS5IaUol64zEDYFVw_naY130_assertion description "[When challenged i.p., mice deficient in either MPO or NE were markedly more susceptible to bacterial infection and death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217640.RAt3G0BNm1xdwR5k8xzxaGgSiS5IaUol64zEDYFVw_naY130_provenance.
NP217641.RApDBSsozX2o54Yx79vtKZWhg9--4pJggPkZ2K_43U4bI130_assertion description "[Bartter's syndrome (BS) is an inherited disease of renal potassium wasting characterized by hypokalemic alkalosis, normal blood pressure, vascular insensitivity to pressor agents and elevated plasma concentrations of renin and aldosterone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217641.RApDBSsozX2o54Yx79vtKZWhg9--4pJggPkZ2K_43U4bI130_provenance.
NP217653.RAsBOHZ3M35eQVUL9BOtMSY7_QfMRz51oKqX0f1f6-WwM130_assertion description "[Despite a spontaneous regression in most of the cases, TMD can be fatal or lead to the subsequent development of myeloid leukemia in 20% of DS children (DS ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217653.RAsBOHZ3M35eQVUL9BOtMSY7_QfMRz51oKqX0f1f6-WwM130_provenance.
NP217654.RAi7yNFIRvpRMtIElr0euL17eupOmHHOglnVD_QW8atz8130_assertion description "[In 2007 it is well established that mutations in DNA repair genes (MLH1, MSH2, MSH6, MYH) and Wnt pathway signal transduction inhibitors (APC) underlie a significant percentage of hereditary CRC susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217654.RAi7yNFIRvpRMtIElr0euL17eupOmHHOglnVD_QW8atz8130_provenance.
NP217659.RAucVvy9Cr41yYRONsYJb3SEdrA_TBKoppF5QGFfabyYk130_assertion description "[The purpose of this study was to determine the pharmacogenetic effects of complement factor H (CFH) Y402H, LOC387715 and high-temperature requirement factor A1 (HTRA1) genotypes on the treatment of exudative age-related macular degeneration (AMD) by intravitreal bevacizumab injection in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217659.RAucVvy9Cr41yYRONsYJb3SEdrA_TBKoppF5QGFfabyYk130_provenance.
NP217662.RAtvIPG3eRXZHT4GBKsxyPwwxoNoMHJE5iDkT9hFn91go130_assertion description "[Utilizing neuroendocrine tumor samples, we found that the frequency as well as the average intensity of the expression of PAX5 increased from pulmonary carcinoid (9%, moderate and strong PAX5 expression, n=44), to large-cell neuroendocrine carcinoma (LCNC, 27%, n=11) to SCLC (33%, n=76).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217662.RAtvIPG3eRXZHT4GBKsxyPwwxoNoMHJE5iDkT9hFn91go130_provenance.
NP217663.RAnQSE--I8c_peuuaHaiVHp32AXOiOft4ehkNdlfd_au0130_assertion description "[Proliferative defects in dyskeratosis congenita skin keratinocytes are corrected by expression of the telomerase reverse transcriptase, TERT, or by activation of endogenous telomerase through expression of papillomavirus E6/E7 or the telomerase RNA component, TERC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217663.RAnQSE--I8c_peuuaHaiVHp32AXOiOft4ehkNdlfd_au0130_provenance.
NP217668.RAu8PIX74Nq2tEjDauwjHzvsQsuHf5cOiUEAYuKLAZTCc130_assertion description "[Association of HPC2/ELAC2 polymorphism with prostate cancer risk in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217668.RAu8PIX74Nq2tEjDauwjHzvsQsuHf5cOiUEAYuKLAZTCc130_provenance.
NP217671.RAps-CQI0TcykEW0m9xBxl9dl6x-URzl9ceal5qB8A8Io130_assertion description "[To date over 40 disease mutations and 9 nonsynonymous polymorphisms in POLG have been found to be associated with autosomal recessive and dominant progressive external ophthalmoplegia (PEO), Alpers syndrome, sensory ataxia, neuropathy, dysarthria and ophthalmoparesis (SANDO), Parkinsonism, and male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217671.RAps-CQI0TcykEW0m9xBxl9dl6x-URzl9ceal5qB8A8Io130_provenance.
NP217673.RAmGfIpcp4rzz3PT4AcZDN-8eFZIBCmfFv_b-2JvN5XtE130_assertion description "[The presence of inhibitors of the Taq DNA polymerase was monitored by spiking aliquots of the above CSF samples with 3 infectious units each of HSV-1 and HSV-2 or HCMV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217673.RAmGfIpcp4rzz3PT4AcZDN-8eFZIBCmfFv_b-2JvN5XtE130_provenance.
NP217682.RArptwySvQt4c_9cjNpO82ThQ49N6Xm84S90gmy-4j8y8130_assertion description "[These data indicate that alterations of p73, including mutations, changes in message abundance, and changes in allelic expression, are likely to be rare in early-stage prostate cancer, and that p73 could be a tissue-specific imprinting gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217682.RArptwySvQt4c_9cjNpO82ThQ49N6Xm84S90gmy-4j8y8130_provenance.
NP217685.RArWzWcCXMq1xfVws1si_6Enu023qHPAe9U_1EGb7FGkQ130_assertion description "[We investigated the association of human leukocyte antigen (HLA) II (DRB1 and DQB1) alleles with susceptibility to human papillomavirus (HPV)-associated cervical precancer and cancer cases in a hospital-based case-control study in a northern Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217685.RArWzWcCXMq1xfVws1si_6Enu023qHPAe9U_1EGb7FGkQ130_provenance.
NP217688.RAo9aEAqlI6PrkbiCrRmZYka3Uv8kdR4NBG86Kl1Em950130_assertion description "[Frequency of a mutated CCR-5 allele (delta32) among Italian healthy donors and individuals at risk of parenteral HIV infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217688.RAo9aEAqlI6PrkbiCrRmZYka3Uv8kdR4NBG86Kl1Em950130_provenance.
NP217692.RAq0qihpK79HgnxXcuViWnEkRd4yj6xqbN9mNdALdrfvg130_assertion description "[Patients with generalized atrophic benign epidermolysis bullosa (GABEB), an inherited subepidermal blistering disease, often have no immunologically detectable bullous pemphigoid antigen 2 (BPAG2) in their epidermal basement membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217692.RAq0qihpK79HgnxXcuViWnEkRd4yj6xqbN9mNdALdrfvg130_provenance.
NP217698.RAsvpaKNzTmE9mvQYIFG-jNtC9FPnRs07b9KqZAHfWcTo130_assertion description "[The gene diagnosis of N-acetyltransferase 2 suggested that the type was classified as NAT2*6A/*7B, indicating that the patient was a slow acetylator.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217698.RAsvpaKNzTmE9mvQYIFG-jNtC9FPnRs07b9KqZAHfWcTo130_provenance.
NP217699.RAqoL-RkC55DASWr3Meef7jQt5S_KldH1ZbHd3sugEY2I130_assertion description "[In contrast to the human syndrome, CSB-deficient mice show increased susceptibility to skin cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217699.RAqoL-RkC55DASWr3Meef7jQt5S_KldH1ZbHd3sugEY2I130_provenance.
NP217704.RAnNAxabkz4TVmUQSJa9Do0dCUgfHkaotxtQlX7gFjBCU130_assertion description "[WS results in visual/spatial processing defects, cognitive impairment, unique behavioral phenotypes, characteristic `elfin` facial features, low muscle tone and heart defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217704.RAnNAxabkz4TVmUQSJa9Do0dCUgfHkaotxtQlX7gFjBCU130_provenance.
NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_assertion description "[In order to determine whether there are phenotypic differences between patients whose PWS is caused by these two different mechanisms, 54 affected individuals (37 with deletion, 17 with UPD) were personally examined and studied using molecular techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217705.RAqQLX15k52NE9SvlPbDIL6BhUBmSd6S-ieQlHfyHa2Pc130_provenance.
NP217708.RAhHNK4cVJmeebCqRdW_gWvGKvz7M-5WrJz5sd3cGXUy8130_assertion description "[In the Mediterranean population, we found suggestive evidence that RECQL4, a gene involved in genome stability, RTEL1, a gene regulating telomere elongation, and TERF2, a gene implicated in the protection of telomeres, were associated with melanoma, the presence of dysplastic nevi and number of nevi, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217708.RAhHNK4cVJmeebCqRdW_gWvGKvz7M-5WrJz5sd3cGXUy8130_provenance.
NP217709.RAkedvfUaGganSxMSEMfvYZsX1qAx-tk1W3eH6-_Y2ZFs130_assertion description "[The last TD patient, found to be heterozygous for a known mutation (p.D1009Y), had a complete defect in ABCA1-mediated cholesterol efflux in fibroblasts, suggesting the presence of a second undetected mutant allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217709.RAkedvfUaGganSxMSEMfvYZsX1qAx-tk1W3eH6-_Y2ZFs130_provenance.
NP217713.RAgOVFEKJsWajr2XdbbJo0VGXBeD5wNiBPPda8OQ7h_JU130_assertion description "[The neuropathology of MOPD I/III is little understood, especially in comparison to other forms of lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217713.RAgOVFEKJsWajr2XdbbJo0VGXBeD5wNiBPPda8OQ7h_JU130_provenance.
NP217721.RAngcWNVhqolXVOYQIupIs6nxiPSMDld4A1v_HoZJT4ck130_assertion description "[DHA also inhibits AKT(T308) but not AKT(S473) phosphorylation, alters PI(3,4,5)P3 (PIP3) and phospho-AKT(S473) protein localization, decreases pPDPK1(S241)-AKT and AKT-BAD interaction and suppresses prostate tumor growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217721.RAngcWNVhqolXVOYQIupIs6nxiPSMDld4A1v_HoZJT4ck130_provenance.
NP217724.RAiAe38w_FEx2ujDHVPCQZ2mQgnWgOosp6KsSa0V-hT1A130_assertion description "[Apart from viral factors, CYP2E1 polymorphism might be associated with increased risk of liver diseases in Northeast India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217724.RAiAe38w_FEx2ujDHVPCQZ2mQgnWgOosp6KsSa0V-hT1A130_provenance.
NP217727.RAkozn8x0w66hOCY-qfB9sSPUbjQUHkH8GdrezOh9dMeY130_assertion description "[Metastasis-associated lung adenocarcinoma transcript 1(MALAT1), a long non-coding RNA (lncRNA), is up-regulated in many solid tumors and associated with cancer metastasis and recurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217727.RAkozn8x0w66hOCY-qfB9sSPUbjQUHkH8GdrezOh9dMeY130_provenance.
NP217731.RAtN2YZZ4NyDlGGvNf5wPMzIUAL_e83dqJoJOxJSuq5OA130_assertion description "[Neither tankyrase nor Rap1 was upregulated in cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217731.RAtN2YZZ4NyDlGGvNf5wPMzIUAL_e83dqJoJOxJSuq5OA130_provenance.
NP217732.RAnqlFrS6WNGflqZOHlSwRm8zBeuCspHO_Yhf4swzfIyg130_assertion description "[To our knowledge, our patient is the first with NBS reported in the literature who was successfully treated for diffuse large B-cell lymphoma with the anti-CD20 monoclonal antibody rituximab in addition to a modified dose of CHOP (cyclophosphamide/doxorubicin/vincristine/prednisone) chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217732.RAnqlFrS6WNGflqZOHlSwRm8zBeuCspHO_Yhf4swzfIyg130_provenance.
NP217737.RAtrd62NT76RSOk7JekgTtI5HzEEDN1SEULjgiW2zy8zE130_assertion description "[At present, there are ample indications that NK cells can eradicate acute myeloid leukemia blasts in patients with a favorable combination of HLA and KIR genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217737.RAtrd62NT76RSOk7JekgTtI5HzEEDN1SEULjgiW2zy8zE130_provenance.
NP217743.RAkZfxvUI1HanVopUdLam9qxnTz40HcG81O9VAkjMgGCk130_assertion description "[This result is complementary to that previously described for the chimeric virus HSV-2 333/LAT1 and indicate that the HSV-1 latency phenotype can be changed to that of HSV-2 by substitution of a 2.8-kb piece of complementary viral DNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217743.RAkZfxvUI1HanVopUdLam9qxnTz40HcG81O9VAkjMgGCk130_provenance.
NP217747.RAoe0bKYdL1PCOSWYnKOjIRuQGJH3wAE65XleHnKE3m34130_assertion description "[In FRG1 mice and FSHD patients, the Calpain 3 isoform lacking exon 6 (Capn3 E6-) is increased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217747.RAoe0bKYdL1PCOSWYnKOjIRuQGJH3wAE65XleHnKE3m34130_provenance.
NP217749.RAnvNi4V2d6M4SJ9lnFZ04bCUK_O5td2mer_SZ7lw0fxo130_assertion description "[Thus, our data indicate that physical interaction and synergy between GATA1 and RUNX1 are retained in DS-AMKL, although it is still possible that increased RUNX1 activity plays a role in the development of leukemia in DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217749.RAnvNi4V2d6M4SJ9lnFZ04bCUK_O5td2mer_SZ7lw0fxo130_provenance.
NP217750.RAo20B4VT_BK1mx83FJ4K9v_--jsrO9URh4y8DLpQxiqg130_assertion description "[Evidence from a carefully designed prospective longitudinal study on a Mexican cohort of HIV/AIDS patients, not receiving anti-retroviral treatment, revealed that the onset of oral candidiasis and oral hairy leukoplakia was heralded by a sustained reduction of CD4+, with an associated sharp increase in viral load.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217750.RAo20B4VT_BK1mx83FJ4K9v_--jsrO9URh4y8DLpQxiqg130_provenance.
NP217756.RAlV6rkjfpmYqUic-reaG40b-GmwBPLVsMn-cv9_yrtAM130_assertion description "[Our array-based analyses of gene expression in patients with chronic myeloid leukemia (CML) revealed several genes (MMP8, MMP9, PCNA, JNK2, MAPK p38) with significant increased expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217756.RAlV6rkjfpmYqUic-reaG40b-GmwBPLVsMn-cv9_yrtAM130_provenance.
NP217760.RApxKLU86hY3rMK8KJfAl3qT7vZnSBU7TVnZfIAk7sUfI130_assertion description "[Three distinct clinical manifestations of carnitine palmitoyltransferase II (CPT II) deficiency have been defined including a mild adult onset myopathy, a severe infantile disorder and a lethal neonatal form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217760.RApxKLU86hY3rMK8KJfAl3qT7vZnSBU7TVnZfIAk7sUfI130_provenance.
NP217761.RArtd0vWUPgw9Z13TwTsSletPkm8_BPDBEtpqWNZEqLV4130_assertion description "[To understand the leukemogenic chromatin signature, we analyzed acute promyelocytic leukemia, a subtype of leukemia characterized by the expression of RARα-fusion proteins, such as PML-RARα.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217761.RArtd0vWUPgw9Z13TwTsSletPkm8_BPDBEtpqWNZEqLV4130_provenance.
NP217764.RAo1_sEJORF8yWPLPPlVC0uHK8qxZCWsJzk2dLsaFA_SU130_assertion description "[To understand the mechanism, telomerase enzymatic activity and telomerase reverse transcriptase (hTERT), gene expression were compared in MDS cases (n=35) and healthy controls (n=42) within different T-cell compartments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217764.RAo1_sEJORF8yWPLPPlVC0uHK8qxZCWsJzk2dLsaFA_SU130_provenance.
NP217774.RAgcFqC4XYx_osDjkZMgKcx_hm_Vf2sYW6eloITWJfJpE130_assertion description "[Alternative splicing of one such gene, the neural cell adhesion molecule CD56 (NCAM), impacts the progression, inadequate therapeutic response, and reduced total survival of patients who suffer from numerous malignant neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217774.RAgcFqC4XYx_osDjkZMgKcx_hm_Vf2sYW6eloITWJfJpE130_provenance.
NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_assertion description "[Moreover, mutations in the TFIIH subunits XPB and XPD found in Cockayne syndrome impair the interaction of TFIIH with the rDNA, but do not influence initiation complex formation or promoter escape of RNA polymerase I, but preclude the productivity of the enzyme by reducing transcription elongation in vivo and in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_provenance.
NP217794.RAqNjHZjqX36tgkyR5tNQqcTm7eqBTD1EW1Ant6BN419o130_assertion description "[The study group consisted of 57 viremic (hepatitis C virus [HCV] 1b) women for whom HLA class II DRB1 and DQB1 haplotyping, virologic, histologic, and biochemical markers of disease activity were available.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217794.RAqNjHZjqX36tgkyR5tNQqcTm7eqBTD1EW1Ant6BN419o130_provenance.
NP217796.RAq-Kb_SNgCpH9mXV1LhhwWc6FpEBTNyxNuEdVXy_V5tE130_assertion description "[In our population, HLA-DRB1*0301 was associated with an increased risk for CD, while HLA-DRB1*1501 conferred protection from the disease (OR: 7.38 and 0.06, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217796.RAq-Kb_SNgCpH9mXV1LhhwWc6FpEBTNyxNuEdVXy_V5tE130_provenance.
NP217797.RAjt1z5KHQxZHpc5oKsJvfEu4ySO6Bh6kangh6ZTzYnZk130_assertion description "[Intragenic polymorphisms in COL7A1 and flanking microsatellite markers on chromosome 3p21, as well as detection of pathogenetic mutations in families, were used to perform PCR-based prenatal diagnosis from DNA obtained by chorionic villus sampling at 10-15 weeks or amniocentesis at 12-15 weeks gestation in 10 families at risk for recurrence of RDEB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217797.RAjt1z5KHQxZHpc5oKsJvfEu4ySO6Bh6kangh6ZTzYnZk130_provenance.
NP217800.RAl3-e_UbH7mQb_U9jjheo0_cSU0WVhwbSA_iF04RwTS0130_assertion description "[Both AP1 and NF-kappaB, transcription factors that regulate IL-2 gene expression, were activated in vivo in sarcoid pulmonary CD4(+) T lymphocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217800.RAl3-e_UbH7mQb_U9jjheo0_cSU0WVhwbSA_iF04RwTS0130_provenance.
NP217802.RAsexz3TFuS5Sj14_GNRU1TTb5aqM4CpYFCCheteioMNo130_assertion description "[These results show that periodontitis lesions in AIDS patients can be characterized by a rapid macrophage turnover, and these HIV-infected macrophage exudates in GCF may be considered as a within-mouth source of virus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217802.RAsexz3TFuS5Sj14_GNRU1TTb5aqM4CpYFCCheteioMNo130_provenance.
NP217805.RAtPi7-Vnx55PLLKkzl4ZysgRiM86XCH83IkJPUsBwqr8130_assertion description "[A polymorphism in the TCF7 gene, C883A, is associated with type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217805.RAtPi7-Vnx55PLLKkzl4ZysgRiM86XCH83IkJPUsBwqr8130_provenance.
NP217807.RAsEVzzv5LsIVeTxWA7nu7iwk9u2T2sTAZYHJxJVnmzCg130_assertion description "[EphA2 receptor tyrosine kinase is frequently overexpressed and functionally altered in a variety of human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217807.RAsEVzzv5LsIVeTxWA7nu7iwk9u2T2sTAZYHJxJVnmzCg130_provenance.
NP217810.RAut5zcd588BSlFAIFECd7cx25ydWOW-lfY7emOYzAMU4130_assertion description "[Cyclin-dependent kinase inhibitor type 2A (CDKN2A) has been identified as a major melanoma susceptibility gene based on the presence of germline mutations in high-risk melanoma families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217810.RAut5zcd588BSlFAIFECd7cx25ydWOW-lfY7emOYzAMU4130_provenance.
NP217813.RAsm871Ae0vcR4WAAbb0s8omobIMjJkcLmltkMC0GAvsw130_assertion description "[Homozygous deletion and expression of PTEN and DMBT1 in human primary neuroblastoma and cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217813.RAsm871Ae0vcR4WAAbb0s8omobIMjJkcLmltkMC0GAvsw130_provenance.
NP217817.RArv9M2l25pO8s3TsV93v0QhNC9J-jUqlU113ZU29fw1w130_assertion description "[Infection with gram-negative monocytotropic Ehrlichia strains results in a fatal toxic shock-like syndrome characterized by a decreased number of Ehrlichia-specific CD4(+) Th1 cells, the expansion of tumor necrosis factor alpha (TNF-alpha)-producing CD8(+) T cells, and the systemic overproduction of interleukin-10 (IL-10) and TNF-alpha.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217817.RArv9M2l25pO8s3TsV93v0QhNC9J-jUqlU113ZU29fw1w130_provenance.
NP217818.RAkKpf4Grx7vkfoZXfZVHMau6Iultbzasqh5i8FaNiwl4130_assertion description "[NKG2D is a functional marker of CD4+ T cells that produce IL-17 in patients with CD, via costimulation of the TCR and NKG2D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217818.RAkKpf4Grx7vkfoZXfZVHMau6Iultbzasqh5i8FaNiwl4130_provenance.
NP217827.RArlqnrTlrWc4tq3oDr9dTWnrtb3MGzgB1hM9twfcuR9c130_assertion description "[The peripheral levels of IAPP relative to insulin are lower in GDM, a finding similar to that described in type 2 diabetes mellitus (non-insulin-dependent diabetes mellitus).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217827.RArlqnrTlrWc4tq3oDr9dTWnrtb3MGzgB1hM9twfcuR9c130_provenance.
NP217829.RAhf0XI219Nc9-b1g74pB2pHi6cnCs1XwuBva9UTZMfE0130_assertion description "[Mutations in the epsilon-sarcoglycan (SGCE) gene have been found recently to cause myoclonus-dystonia (MD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217829.RAhf0XI219Nc9-b1g74pB2pHi6cnCs1XwuBva9UTZMfE0130_provenance.
NP217835.RAnt_lVXABY4GG5FRB8b6Ahx6LuqWtq1ozTFaplj4W5d0130_assertion description "[In conclusion, this analysis provided to detect some molecular differences between primary metastatic and nonmetastatic CRCs, with K-Ras and p16INK4A statistically altered in metastatic tumours; particular gene combinations, such as coincidental K-Ras mutation with two methylated genes are associated to a metastogenic phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217835.RAnt_lVXABY4GG5FRB8b6Ahx6LuqWtq1ozTFaplj4W5d0130_provenance.
NP217837.RAtReCAMxIzr9PmMY0Hg5riybBiMlKFpxrEaG_k6fRZto130_assertion description "[Mutations in the CLN2 gene result in classical late infantile neuronal ceroid lipofuscinosis (LINCL), a fatal childhood neurodegenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217837.RAtReCAMxIzr9PmMY0Hg5riybBiMlKFpxrEaG_k6fRZto130_provenance.
NP217838.RAkZRWZRf2b4lzZFvvSZaXBmbxtgmz9qyq-mlBKDRad4Y130_assertion description "[Furthermore, we studied the pathophysiological role of HGF in a myocardial infarction model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217838.RAkZRWZRf2b4lzZFvvSZaXBmbxtgmz9qyq-mlBKDRad4Y130_provenance.
NP217839.RAgdxJP-wKykiv3SwEMyddgNPFKKIfA7jPXBml_TX9Qqk130_assertion description "[Given the role of even-skipped homeobox 1 (EVX1) in the regulation of multiple genes during embryogenesis, we postulated that EVX1 methylation is altered in PCa progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217839.RAgdxJP-wKykiv3SwEMyddgNPFKKIfA7jPXBml_TX9Qqk130_provenance.
NP217840.RAhda7pr4SWPT4ToobeUtH3nJ6CnWoCHwSgeDMaBTWkCk130_assertion description "[Tyrosinase, the primary enzyme in melanin synthesis commonly mutated in albinism, oxidizes l-tyrosine to l-dopaquinone using l-3,4-dihydroxyphenylalanine (L-DOPA) as an intermediate product.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217840.RAhda7pr4SWPT4ToobeUtH3nJ6CnWoCHwSgeDMaBTWkCk130_provenance.
NP217850.RAieR9nrmC8XY6s-VsuQEa7jvyi9dCIld4MmUxCHWgoUU130_assertion description "[Seven out of nine patients had a mutation on codon 634 of exon 11 of RET (TGC-CGC), leading to cysteine arginine substitution in the codified protein; all gene carriers had biochemical markers of MTC/CCH and four of Pheo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217850.RAieR9nrmC8XY6s-VsuQEa7jvyi9dCIld4MmUxCHWgoUU130_provenance.
NP217854.RAisAmVjvOWwO6XHiFhfd4-2oxTNeqEmnKnFbrZnL0zAE130_assertion description "[Trichostatin A reverses skewed expression of CD154, interleukin-10, and interferon-gamma gene and protein expression in lupus T cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217854.RAisAmVjvOWwO6XHiFhfd4-2oxTNeqEmnKnFbrZnL0zAE130_provenance.
NP217855.RAvMNujxLUO90E4YMvsPLeMMHPuL1I7_vROV5f2GjIw5g130_assertion description "[The genetic polymorphism of p53 codon 72 Arg/Pro has been implicated in oral cancer risk, but the results of previous studies remain controversial and ambiguous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217855.RAvMNujxLUO90E4YMvsPLeMMHPuL1I7_vROV5f2GjIw5g130_provenance.
NP217862.RAi_yZWAsFGukYJ0mkOnMj7ccrpparEd69aYZXwgjxsoY130_assertion description "[The reciprocal translocation t(1;3)(p36;q21) is associated with myelodysplastic syndromes (MDSs) and acute myeloid leukemia (AML) characterized by trilineage dysplasia, in particular dysmegakaryocytopoiesis, and a poor prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217862.RAi_yZWAsFGukYJ0mkOnMj7ccrpparEd69aYZXwgjxsoY130_provenance.
NP217865.RAuZ6i0L-X2-OG2EvqLTVGOw067Ck8cVsrifpHjSgw6kM130_assertion description "[Five single nucleoside polymorphisms of the TPH1 gene were studied in a population-based sample of postpartum Taiwanese women consisting of 120 subjects with depression or/and anxiety and 86 matched normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217865.RAuZ6i0L-X2-OG2EvqLTVGOw067Ck8cVsrifpHjSgw6kM130_provenance.
NP217871.RAl9daT1YiygvZHgoTbgSOKs_t9r3lP6Q-NrCEnEFSLaQ130_assertion description "[Protein expression analysis of chronic lymphocytic leukemia defines the effect of genetic aberrations and uncovers a correlation of CDK4, P27 and P53 with hierarchical risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217871.RAl9daT1YiygvZHgoTbgSOKs_t9r3lP6Q-NrCEnEFSLaQ130_provenance.
NP217873.RAsw06V70hgMUyE-LW3haATgmHOyNX9KgRHPirofx8tKs130_assertion description "[Irrespective of the differences of gross and morphological pattern, majority (54/74) of cancer cases expressed multiple RHAMM isoforms in Mr 40000-45000, 64000, 70000-73000, 85000 and 93000-95000 with the appearance of cell surface immunocytochemical labeling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217873.RAsw06V70hgMUyE-LW3haATgmHOyNX9KgRHPirofx8tKs130_provenance.
NP217879.RAqAaNtrP1H6UU17B41d63367elVWx-MkmIpa4l7apRPg130_assertion description "[In conclusion, we found that human meningiomas express CXCR4 and SDF1 and that hSDF1alpha induces proliferation in primary meningioma cell cultures through the activation of ERK1/2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217879.RAqAaNtrP1H6UU17B41d63367elVWx-MkmIpa4l7apRPg130_provenance.
NP217880.RAgaIgfzISKBY01FMnHoRGCisL5P4SUBlQrcOlxkakNdA130_assertion description "[We examined the association of 13 variants in eight genes (rs4646903, rs2031920, rs3813867, GSTM1 null, GSTT1 null, rs1695, rs1138272, rs1799782, rs25487, rs1799791, rs1799793, rs13181 and rs1052133) involved in various stages of tobacco and alcohol metabolism and the risk of leukoplakia and oral cancer (OC) in a case-control study involving 219 oral leukoplakia, 665 OC and 802 age, sex and habit-matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217880.RAgaIgfzISKBY01FMnHoRGCisL5P4SUBlQrcOlxkakNdA130_provenance.
NP217882.RAqQE8DzUuMvo6rFIyPjbE8oN83Ep8qYcGsqBk2jzCm2U130_assertion description "[These techniques enable the performance of liver transplantation with ABO blood group compatible organs of almost any size if indicated either by deterioration of liver function or impending complications such as hepatoma or life-threatening progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217882.RAqQE8DzUuMvo6rFIyPjbE8oN83Ep8qYcGsqBk2jzCm2U130_provenance.
NP217887.RAggbcDygH0SaYaw2rxLJO_hlqHeMioTZMlnm71Jkebf8130_assertion description "[We report here that in breast carcinoma, estrogen may induce tumor development by eliciting protease-activated receptor-1 (PAR(1)) gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217887.RAggbcDygH0SaYaw2rxLJO_hlqHeMioTZMlnm71Jkebf8130_provenance.
NP217888.RAm4IOrhNVC95ycFSWuxpphBXUiJ2birmdcZyV04Sv0NE130_assertion description "[Muscle PC-1 content was similar in the insulinoma patients and in insulin sensitive controls but higher (p<0.01) in insulin resistant controls (21.9+/-4.6 ng/mg protein, 23.8+/-3.9, 48.0+/-8.7, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217888.RAm4IOrhNVC95ycFSWuxpphBXUiJ2birmdcZyV04Sv0NE130_provenance.
NP217899.RAmYRv7lqKixTId1QKdEBPEH05PL_pwwhh1B0QB5I3p5Y130_assertion description "[Mx1-Cre, 5A3(fl) mice show normal hematologic parameters and do not spontaneously develop myeloid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217899.RAmYRv7lqKixTId1QKdEBPEH05PL_pwwhh1B0QB5I3p5Y130_provenance.
NP217900.RAtKjRVflZuIZf1XpJuazqkhkwHOYBnHIoy1sCLMUwHdw130_assertion description "[In further stratified analysis, we found that MTHFR 677 CT contributed to elevated risk of cleft lip only, as did MTHFR 677 CT/TT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217900.RAtKjRVflZuIZf1XpJuazqkhkwHOYBnHIoy1sCLMUwHdw130_provenance.
NP217901.RAlLQ74GW4N7fMS90r1vtlvPWaCy5NQ67MlJ4y_4lPOpU130_assertion description "[Validation with the two independent datasets demonstrated that the malignancy-risk score had prognostic and predictive values: Of patients who did not receive ACT, those with a low malignancy-risk score had increased OS compared with a high malignancy-risk score (P = .007 and .01 for the GSE13212 and GSE14814 datasets, respectively), indicating a prognostic value; and in the GSE14814 dataset, patients receiving ACT survived longer in the high malignancy-risk score group (P = .03), and a statistically significant interaction between ACT and the signature was observed (P = .02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217901.RAlLQ74GW4N7fMS90r1vtlvPWaCy5NQ67MlJ4y_4lPOpU130_provenance.
NP217905.RAqQtmuQIj20tomEgXDB81paVInaHNvLXO_vKGcGHkuXQ130_assertion description "[This genetic alteration results in reduced levels of the SMN protein, leading to degeneration of alpha motor neurons of the spinal cord and resulting in muscle weakness and progressive symmetrical proximal paralysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217905.RAqQtmuQIj20tomEgXDB81paVInaHNvLXO_vKGcGHkuXQ130_provenance.
NP217908.RArk11K5HnOrljY_H4Y-hPQVsXC9JHOaqquvklOEm097k130_assertion description "[The association of the T8590C variant with hypertension supports its role as a polygenic determinant of blood pressure control in humans, and results obtained from the large population database suggest that the relevance of the variant may vary according to hypertension comorbidity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217908.RArk11K5HnOrljY_H4Y-hPQVsXC9JHOaqquvklOEm097k130_provenance.
NP217909.RAuDSlHS3bLKfJerdS4gAaMxYNY32nVmtFxpC234Ff_ak130_assertion description "[Metastasis-associated protein 1 (MTA1), a component of the nucleosome-remodeling and histone deacetylase complex, is widely up-regulated in human cancers and significantly correlated with tumor invasion and metastasis, but the mechanisms involved remain largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217909.RAuDSlHS3bLKfJerdS4gAaMxYNY32nVmtFxpC234Ff_ak130_provenance.
NP217911.RAvdYP8rLhkhUpdjzXcOe1LJ7yu2lEKhVriUxzA-4MCOE130_assertion description "[A set of 662 FFPE DNA samples not only confirmed that APOLD1 and SRPX2 are hypomethylated in CRC but also revealed hypomethylation to be significantly (p < 0.01) associated with tumors being localized in the left side, CpG island methylator phenotype negative, MSS, BRAF wt, undifferentiated and of adenocarcinoma histosubtype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217911.RAvdYP8rLhkhUpdjzXcOe1LJ7yu2lEKhVriUxzA-4MCOE130_provenance.
NP217917.RAhKl2lv0pM-409lwqe8t30eoXo2CoH__3lEDsUMzKSJQ130_assertion description "[Given the availability of ABCC9 antagonists, our findings may have direct implications for the treatment of individuals with Cantú syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217917.RAhKl2lv0pM-409lwqe8t30eoXo2CoH__3lEDsUMzKSJQ130_provenance.
NP217918.RAkCbEwhoU-GdKgiX0OyhNtLF_QFmifUYdnW0Qfdsejg4130_assertion description "[The results of this study suggest that TNF plays an important role in the pathogenesis of the cytopenia(s) characteristically associated with HCL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217918.RAkCbEwhoU-GdKgiX0OyhNtLF_QFmifUYdnW0Qfdsejg4130_provenance.
NP217929.RAmD2TVNDcLWSbnYDVGDSC-tbCtVcVwZi8-OM8UsWARfI130_assertion description "[CBL mutations in myeloproliferative neoplasms are also found in the gene's proline-rich domain and in patients with the V617FJAK2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217929.RAmD2TVNDcLWSbnYDVGDSC-tbCtVcVwZi8-OM8UsWARfI130_provenance.
NP217932.RAruqk1bKkaVIrMJ6gqlLREBVD6SedXwo91gVdWMR-q3g130_assertion description "[Moreover, Kaposi sarcoma-associated herpesvirus (KSHV)-encoded viral FLICE inhibitory protein (vFLIP) enhances IRF4-mediated gene induction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217932.RAruqk1bKkaVIrMJ6gqlLREBVD6SedXwo91gVdWMR-q3g130_provenance.
NP217933.RAnnMxHAfZFKCW5DVLO1ij61c49SYDNXyiRlhJa9eU6oc130_assertion description "[The recessively inherited deficiency of acid alpha-glucosidase (GAA) called Glycogenosis Type II is expressed as three different phenotypes: infantile, juvenile, and adult.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217933.RAnnMxHAfZFKCW5DVLO1ij61c49SYDNXyiRlhJa9eU6oc130_provenance.
NP217936.RAua5L04k-Eo34uiYVZALV7UqA1yWbZCw6LQUyS1G1QnY130_assertion description "[Lck-TSLP;CD11b-DTR mice, with or without toxin treatment, had similar levels of cryoglobulinemia and glomerular immunoglobulin deposition as Lck-TSLP mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217936.RAua5L04k-Eo34uiYVZALV7UqA1yWbZCw6LQUyS1G1QnY130_provenance.
NP217939.RAu2BYygRPaz0nQ0kSvs2Y_xDn38npWuaJRttWAuKRVSQ130_assertion description "[The impact of alcohol and polymorphisms in aldehyde dehydrogenase 2 (ALDH2) Glu504Lys, alcohol dehydrogenase (ADH) 1B His48Arg, and ADH1C Arg272Gln on PC risk was examined with multivariate analysis adjusted for potential confounders to estimate odds ratios (ORs) and 95% confidence intervals (CIs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217939.RAu2BYygRPaz0nQ0kSvs2Y_xDn38npWuaJRttWAuKRVSQ130_provenance.
NP217941.RAuIR3yYTu7oxv3eKwNj6StKnBrt1CtdqloFO7f4yEfdg130_assertion description "[To better define IDH1 and IDH2 mutational status, an additional 75 gallbladder and bile duct cancers were examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217941.RAuIR3yYTu7oxv3eKwNj6StKnBrt1CtdqloFO7f4yEfdg130_provenance.
NP217944.RAn5SWIaB1p1RSlZKLqV0aJOzPTZUoMQglRUmGvBhib9o130_assertion description "[Among 6,565 consecutive abnormal cytogenetic reports at our institution, 3,192 (49%) constituted sole abnormalities, of which 230 (7%) involved chromosome 7: monosomy 7 (n = 98), 7q- (n = 51), der(1;7)(q10;p10) (n = 44), balanced translocations (n = 15), ring 7 (n = 13), and 7p- (n = 9).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217944.RAn5SWIaB1p1RSlZKLqV0aJOzPTZUoMQglRUmGvBhib9o130_provenance.
NP217953.RAkw-Xb4n_jjC73cOln87oadByVIh2YIaREC9k_OhJKG0130_assertion description "[KCNJ5 sequencing was performed on somatic (APA, n=380) and peripheral (APA, n=344; bilateral adrenal hyperplasia, n=174) DNA of patients with primary aldosteronism, collected through the European Network for the Study of Adrenal Tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217953.RAkw-Xb4n_jjC73cOln87oadByVIh2YIaREC9k_OhJKG0130_provenance.
NP217954.RArbWC9ERz0yiNDCJUxuvh6h4-u2-449WOJAtM5A6uXI0130_assertion description "[We previously showed that S100P positive gastric cancer patients have a better cumulative survival than S100P negative patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217954.RArbWC9ERz0yiNDCJUxuvh6h4-u2-449WOJAtM5A6uXI0130_provenance.
NP217956.RAuGXECKrm15rULkgwWA-aPHhYAsa22_aqgs0rvRVzuWU130_assertion description "[We describe a patient with congenital hyperinsulinism with previously unreported pathological findings including normal to decreased number of insulin-positive cells with very few enlarged nuclei, aberrant distribution of glucagon-positive cells, and a non-insulin producing adenomatous focus of unusual morphology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217956.RAuGXECKrm15rULkgwWA-aPHhYAsa22_aqgs0rvRVzuWU130_provenance.
NP217959.RArpu6ozH_3hiJJMBLTdPG8nCurcXkSz84R8sq57V61Tw130_assertion description "[To test the hypothesis that the FA network is conserved in vertebrate genomes, we cloned and sequenced zebrafish (Danio rerio) cDNAs and/or genomic BAC clones orthologous to all nine cloned FA genes (FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL), and identified orthologs in the genome database for the pufferfish Tetraodon nigroviridis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217959.RArpu6ozH_3hiJJMBLTdPG8nCurcXkSz84R8sq57V61Tw130_provenance.
NP217965.RArEee3KGaN5k-dOKF2F28RDZ-wMv9NqpGtFfuVgJucsM130_assertion description "[The IL-23R allele was negatively associated with inflammatory bowel disease (IBD): the R381Q SNP was undertransmitted in children with IBD (8 transmitted [T] versus 27 untransmitted [UT]; P = 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217965.RArEee3KGaN5k-dOKF2F28RDZ-wMv9NqpGtFfuVgJucsM130_provenance.
NP217972.RAphC7LhlTC8t1logV79xRqIBXd7DQ8HZ5_4WzmGee8uM130_assertion description "[rs10927875 maps to a region on chromosome 1p36.13 which encompasses several genes among which HSPB7 has been formerly suggested to be implicated in DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217972.RAphC7LhlTC8t1logV79xRqIBXd7DQ8HZ5_4WzmGee8uM130_provenance.
NP217974.RAq0OCu_5INOJ_VExb33Hecx2EWb8KXfx_zNa9UZsAjzo130_assertion description "[In conclusion, ABCB1 and ABCC2 genotypes modulate the expression in the unaffected renal cortex of RCC patients, possibly contributing to inter-individual differences in drug and xenobiotics elimination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217974.RAq0OCu_5INOJ_VExb33Hecx2EWb8KXfx_zNa9UZsAjzo130_provenance.
NP217977.RAiCvEybV1QW9aOLfCmYJeH-EsZxiSHAedYm6LZx8LZIE130_assertion description "[Studies on the associations between the nitric oxide synthase gene (NOS3) Glu298Asp polymorphism and hypertension status or blood pressure (BP) levels have had inconsistent results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217977.RAiCvEybV1QW9aOLfCmYJeH-EsZxiSHAedYm6LZx8LZIE130_provenance.
NP217978.RArJ3u_VOc5dpqltZZFYCXMqu0T37m5InIWqFNTCgKzCg130_assertion description "[We performed whole exome sequencing in a Turkish patient clinically diagnosed with Alzheimer's disease from a consanguineous family with a complex history of neurological and immunological disorders and identified a mutation in NOTCH3 (p.R1231C), previously described as causing cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217978.RArJ3u_VOc5dpqltZZFYCXMqu0T37m5InIWqFNTCgKzCg130_provenance.
NP217979.RAgxBfjBUHnaVLtveEsTgErx_t8UOnbZ7mV-vpoMAmd6I130_assertion description "[In mammospheres exposed to the breast tumor fibroblasts supernatant, autocrine tumor necrosis factor-α signalling engenders the functional interplay between peroxisome proliferator activated receptor-α and hypoxia inducible factor-1α (PPARα/HIF1α).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217979.RAgxBfjBUHnaVLtveEsTgErx_t8UOnbZ7mV-vpoMAmd6I130_provenance.
NP217982.RAjpLTx7jYxFL3ESzQGc2TpmqOfgCBV0ke1xTxb9rq1a0130_assertion description "[Surface-localized protein antigens (alpha, beta, R1, and R4) serve as additional markers to classify GBS isolates, which is particularly useful since NT isolates often express one or more of these proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217982.RAjpLTx7jYxFL3ESzQGc2TpmqOfgCBV0ke1xTxb9rq1a0130_provenance.
NP217986.RAnga0nCoK_Wx5YeuOq4qD_2qoFsM2cvuRmbWQf78lT50130_assertion description "[GSTM1 and GSTT1 polymorphisms and the risk of prostate cancer in a Caribbean population of African descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217986.RAnga0nCoK_Wx5YeuOq4qD_2qoFsM2cvuRmbWQf78lT50130_provenance.
NP217987.RAvwm6Ms4qsyDPn0gYYU-1h7rtlGOjkuAEBR0txjtl1U4130_assertion description "[Hereditary persistence of fetal hemoglobin (HPFH) is one of the hemoglobinopathies in which the fetal gamma-globin genes remain active in adult life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217987.RAvwm6Ms4qsyDPn0gYYU-1h7rtlGOjkuAEBR0txjtl1U4130_provenance.
NP217995.RAucJqBoNMJ628VmXHpFTtjoc6wwdxQLLO_1MirZmykgY130_assertion description "[Furthermore, genes regulating production of interleukin (IL)-1 influence the risk for both aggressive periodontitis (AgP) and chronic periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217995.RAucJqBoNMJ628VmXHpFTtjoc6wwdxQLLO_1MirZmykgY130_provenance.

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