Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP182295.RAVtiM1Xc49miUZokkg_qRDlqGj4FN33UXxIfZKEq9BxE130_assertion description "[Here, we describe linkage investigations of the VNTR and ADHD in affected sibling pair (ASP) families and singleton families using both the transmission disequilibrium test (TDT) and a mean test of identity-by-descent (IBD) sharing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182295.RAVtiM1Xc49miUZokkg_qRDlqGj4FN33UXxIfZKEq9BxE130_provenance.
- NP182304.RAYpE9UwOkkL8cxOTr-tgEy6JEwfBL1sy2j2tbYnsa-50130_assertion description "[Using cDNA microarrays to identify human CD19(+) B cell gene products (ESTs) originated from systemic lupus erythematosus susceptibility loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182304.RAYpE9UwOkkL8cxOTr-tgEy6JEwfBL1sy2j2tbYnsa-50130_provenance.
- NP182308.RAduDReD9TmKrmuU-_H6PZbT-VW4DqwiMgbRwIIvAp92s130_assertion description "[A reduction in Pten tumor suppressor activity promotes ErbB-2-induced mouse prostate adenocarcinoma formation through the activation of signaling cascades downstream of PDK1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182308.RAduDReD9TmKrmuU-_H6PZbT-VW4DqwiMgbRwIIvAp92s130_provenance.
- NP182310.RAeqRkMpbavr6D6lDM8hLDzbhbkeONbD-AimYnRa3XbSs130_assertion description "[ACTH therapy resulted in prompt remission of seizures and resolution of EEG abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182310.RAeqRkMpbavr6D6lDM8hLDzbhbkeONbD-AimYnRa3XbSs130_provenance.
- NP182312.RAdr1MAwC4-2Hi30p_h03Ccgan5XRJgZwbKkuk1BrJotc130_assertion description "[The aim of this study was to identify proteins associated with PRL-3-promoted colon cancer metastasis, by comparative proteomic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182312.RAdr1MAwC4-2Hi30p_h03Ccgan5XRJgZwbKkuk1BrJotc130_provenance.
- NP182315.RAaPUTr7PUCnuMASwoKxfCnbOAdDjhMSbrQf5gU5Tk_kk130_assertion description "[Association of genetic variation in serum amyloid-A with cardiovascular disease and interactions with IL6, IL1RN, IL1beta and TNF genes in the Cardiovascular Health Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182315.RAaPUTr7PUCnuMASwoKxfCnbOAdDjhMSbrQf5gU5Tk_kk130_provenance.
- NP182323.RAfl4wB-hiho6RY9T_vIR3YEtzy8zmdfruQYSKnuQgyPc130_assertion description "[The identification of a second mutation in the cationic trypsinogen gene (HP2) suggests a dominant role of trypsin in premature protease activation-mediated forms of acute pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182323.RAfl4wB-hiho6RY9T_vIR3YEtzy8zmdfruQYSKnuQgyPc130_provenance.
- NP182326.RAS0bHycvcgYzM9CKemCgLasR21oLN8In8vL1soR33Nxc130_assertion description "[We investigated the presence of high-risk (types 16 and 18) and intermediate-risk (types 31 and 33) human papilloma virus (HPV) sequences, TP53 and K-ras gene mutations, and loss of heterozygosity (LOH) at 9 genes/chromosomal regions, including 3p14.2/FHIT, 3p14-p21, 3p21, 3p22-p24, 5q21-q22/APC-MCC region, 9p21/CDKN2, 11q23/MEN1, 13q/RB, and 17p/TP53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182326.RAS0bHycvcgYzM9CKemCgLasR21oLN8In8vL1soR33Nxc130_provenance.
- NP182328.RAVCVMipy96ttEKFXduReDsn-wojA3p-4fgiPBD9VOwTM130_assertion description "[Erythrokeratodermia variabilis (EKV, OMIM 133200) is an autosomal dominant genodermatosis with considerable intra- and interfamilial variability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182328.RAVCVMipy96ttEKFXduReDsn-wojA3p-4fgiPBD9VOwTM130_provenance.
- NP182333.RAdLpvhFnpm05WTr5AS9fsJdODwQkk1IjaLbeBrJVYsa8130_assertion description "[In hepatitis B virus related hepatocarcinogenesis, p21WAF1/CIP1 and p53 are suggested to be involved in late stage of tumor progression rather than in early stage of dysplastic nodules and p53 is considered to be the main regulator of the cell dynamics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182333.RAdLpvhFnpm05WTr5AS9fsJdODwQkk1IjaLbeBrJVYsa8130_provenance.
- NP182349.RAXlQ618FUvM2S_cLociGAyEydIwTu66MVBCLCo0Zd4B4130_assertion description "[The expression of MIC2 and the genetic rearrangement of EWS-FLI1 are considered to be highly specific to the pPNET/ES.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182349.RAXlQ618FUvM2S_cLociGAyEydIwTu66MVBCLCo0Zd4B4130_provenance.
- NP182353.RAceB3_7Zw8hvdAH8YJxbMsD_sxXdCI6LcG9_qihlBXdY130_assertion description "[Furthermore, the elevated beta-casein antibody levels found in LADA patients suggest that the antibody response to this protein may be relevant in autoimmune diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182353.RAceB3_7Zw8hvdAH8YJxbMsD_sxXdCI6LcG9_qihlBXdY130_provenance.
- NP182354.RAY8kmxjdII42bR7NHXViyRdpvapAEdw1EKtolSkjEM6U130_assertion description "[The increase of the GNAI2 expression significantly inhibits, whereas knockdown of the GNAI2 expression remarkably enhances HCC cell migration and invasion, indicating that GNAI2 functions as a metastasis suppressor in HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182354.RAY8kmxjdII42bR7NHXViyRdpvapAEdw1EKtolSkjEM6U130_provenance.
- NP182355.RAZm9yEpe3HPii1N6k4P2tLhWZlnGOmNRHzlazjnmR0UE130_assertion description "[mRNA expression of WTX from MSI-H and MSS cases and a panel of colorectal cancer cell lines was investigated using reverse transcription (RT-) PCR and FCE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182355.RAZm9yEpe3HPii1N6k4P2tLhWZlnGOmNRHzlazjnmR0UE130_provenance.
- NP182356.RAQV_kGzM9o3PzV1Gncuo_lDFyU2SHF08iwiKhVNz3SBg130_assertion description "[Increased expression of APAF-1 in low-risk myelodysplastic syndrome: a possible role in the pathophysiology of myelodysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182356.RAQV_kGzM9o3PzV1Gncuo_lDFyU2SHF08iwiKhVNz3SBg130_provenance.
- NP182359.RAXSV6jbcrTcTVB__jmEtflaCdRSu6-cDjaslaXpx-zBs130_assertion description "[Although mutations in the endoglin (ENG) and activin A receptor type II-like 1 (ACVRL1) genes have been known to cause HHT for more than 10 yr, little is known about the clinical features or genetic background of Korean patients with HHT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182359.RAXSV6jbcrTcTVB__jmEtflaCdRSu6-cDjaslaXpx-zBs130_provenance.
- NP182373.RAcSA7zwQm_3mwNCvhP-dFx7YjNYrOuKi5cxOLRK6SiN4130_assertion description "[Several mutations in the N terminus of the G-protein-coupled receptor rhodopsin disrupt NXS/T consensus sequences for N-linked glycosylation (located at N2 and N15) and cause sector retinitis pigmentosa in which the inferior retina preferentially degenerates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182373.RAcSA7zwQm_3mwNCvhP-dFx7YjNYrOuKi5cxOLRK6SiN4130_provenance.
- NP182378.RAVJZS6GJx7Tc2cWdi1ayXbTjF92MbrowssGjb6nxD4Wg130_assertion description "[Hypophosphatasia is a rare inherited disorder characterized by defective bone mineralization and deficiency of serum and tissue liver/bone/kidney tissue alkaline phosphatase (L/B/K ALP) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182378.RAVJZS6GJx7Tc2cWdi1ayXbTjF92MbrowssGjb6nxD4Wg130_provenance.
- NP182379.RAebSSkQ7nP2X-E6v7Fllz55IbxF_035gI7VKYuAKAKrc130_assertion description "[Neural tube defects (NTD) are common malformations resulting from incomplete closure of the neural tube in the first month after conception.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182379.RAebSSkQ7nP2X-E6v7Fllz55IbxF_035gI7VKYuAKAKrc130_provenance.
- NP182383.RAY6UniObxYckd_1gaxvYNNzYsVz8camKMCXR0WG2fsDU130_assertion description "[Losses of 1p32.2-p31.3, 10q11.23-q21.1 and 15q21.3 were correlated with tumor recurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182383.RAY6UniObxYckd_1gaxvYNNzYsVz8camKMCXR0WG2fsDU130_provenance.
- NP182384.RAdagWMzkjkyzFWAthpoLqeisibxAc1d3rnIYbDVnNfks130_assertion description "[GSTT1 homozygous null genotype and GSTP1 genotypes were not associated with the risk of gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182384.RAdagWMzkjkyzFWAthpoLqeisibxAc1d3rnIYbDVnNfks130_provenance.
- NP182385.RAZDqpAmQZQEPS4t6G7bRwqnrUx1ZqdeIdrlfluMHIMFU130_assertion description "[In addition, a subgroup of more aggressive tumors can be identified by evaluating Hiwi level in LN- cancer, and SNCG level in LN+ cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182385.RAZDqpAmQZQEPS4t6G7bRwqnrUx1ZqdeIdrlfluMHIMFU130_provenance.
- NP182389.RAeeLcbX0O2QFo-_fBrHFsfkAiG8aIgfdcYiniuXUgn90130_assertion description "[We measured the levels of alpha(1)-antichymotrypsin (ACT), alpha(1)-antitrypsin (AAT), interleukin-6 (IL-6), monocyte chemoattractant protein-1 (MCP-1) and oxidised low-density lipoprotein (oxLDL) in matched cerebrospinal fluid (CSF) and plasma of 141 patients with probable AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182389.RAeeLcbX0O2QFo-_fBrHFsfkAiG8aIgfdcYiniuXUgn90130_provenance.
- NP182399.RAdBZbAhwwG2opTv9s4IsFXPbyALy4gDJLbWgj705w6XM130_assertion description "[Association study of interferon-γ, cytosolic phospholipase A2, and cyclooxygenase-2 gene polymorphisms in Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182399.RAdBZbAhwwG2opTv9s4IsFXPbyALy4gDJLbWgj705w6XM130_provenance.
- NP182410.RAS34bJ0DfEhSD0cGZwjsei0LUmIP_q9KVYZ2l4Vjo7iY130_assertion description "[Pharmacological activation or inhibition of ERα and/or ERβ provides already the basis for many therapeutic interventions, from contraception or hormone replacement at menopause to prevention of the recurrence of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182410.RAS34bJ0DfEhSD0cGZwjsei0LUmIP_q9KVYZ2l4Vjo7iY130_provenance.
- NP182422.RATuOMFHHrE1veK0RP9HyREC-8DAYdLphFlCQMze1Rf6I130_assertion description "[We present the physical history, clinical presentation, diagnosis and treatment of a patient with a novel germline APC mutation, the W421X mutation, which resulted in FAP presenting with about a hundred colorectal polyps, gastric hyperplastic polyps and multiple aggressive intra-abdominal and extra-abdominal desmoid tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182422.RATuOMFHHrE1veK0RP9HyREC-8DAYdLphFlCQMze1Rf6I130_provenance.
- NP182426.RAX-FRKJ2zTK86Ah9PomUhEwjCF8kuXQrat9Irz2nNxG0130_assertion description "[Relationship between the p27Kip1 (here after referred to as p27) V109G polymorphism and cancer risk has been extensively studied; however, results from different studies were not fully consistent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182426.RAX-FRKJ2zTK86Ah9PomUhEwjCF8kuXQrat9Irz2nNxG0130_provenance.
- NP182428.RAQM_8axIMJwbEtm4XrGHZZObzMO_qhqJAKY8ylfPjwZ0130_assertion description "[Expression of the calcitonin (CT)/calcitonin gene related peptide (CGRP) gene and the proopiomelanocortin (POMC) gene has been demonstrated by Northern blot hybridization analysis of RNA extracted from human medullary thyroid carcinoma (MTC), pheochromocytoma and lung carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182428.RAQM_8axIMJwbEtm4XrGHZZObzMO_qhqJAKY8ylfPjwZ0130_provenance.
- NP182431.RAckw_NcGECTj-i5EzYgRtwUBhYbV7KXFdytmMRglXAa4130_assertion description "[Proinflammatory cytokines cause FAT10 upregulation in cancers of liver and colon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182431.RAckw_NcGECTj-i5EzYgRtwUBhYbV7KXFdytmMRglXAa4130_provenance.
- NP182434.RAcwKWpo_StkwyS6b1CQvo-v-LeHel9mpeSP8SKgaGml4130_assertion description "[Complete elimination of colorectal tumor xenograft by combined manganese superoxide dismutase with tumor necrosis factor-related apoptosis-inducing ligand gene virotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182434.RAcwKWpo_StkwyS6b1CQvo-v-LeHel9mpeSP8SKgaGml4130_provenance.
- NP182443.RAX7QztAZaxXp44fXf1NSixe4Pnl8rfIGZBTFondQr5PA130_assertion description "[Our study implies that overexpression of EcSOD is a promising strategy to enhance the efficacy of heparin/LMWH by inhibiting heparanase as a novel treatment for breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182443.RAX7QztAZaxXp44fXf1NSixe4Pnl8rfIGZBTFondQr5PA130_provenance.
- NP182445.RAX8mxS3fSraPGoY-GwGLAKkoazT9s2yaFszrAw39dLTU130_assertion description "[published in The Journal of the National Cancer Institute (Vol., 2006) new insight is provided of three specific molecular compounds: hypoxia-inducible factor-1alpha (HIF-1alpha), the connective tissue growth factor (CTGF) and the vascular endothelial growth factor-A (VEGF-A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182445.RAX8mxS3fSraPGoY-GwGLAKkoazT9s2yaFszrAw39dLTU130_provenance.
- NP182450.RAYqQk5vm03Z1DB0RNZmh7ZeEHoY1v_Za_dByk0symIPA130_assertion description "[The present study examined the involvement of +138 insA/delA and G198T ET-1 polymorphisms with emphysematous and bronchitic COPD phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182450.RAYqQk5vm03Z1DB0RNZmh7ZeEHoY1v_Za_dByk0symIPA130_provenance.
- NP182453.RAcKdy_oiRfZqy6z6V-9--T32_x4ifEIbyn3cVQvVuUtw130_assertion description "[The RET protooncogene plays a crucial role in neural crest development; accordingly, mutations of RET cause MEN2A and familial medullary thyroid carcinoma, while the expression deregulation of RET is involved in the pathophysiology of glioblastoma multiforme (GBM) and pancreatic cancer (PDAC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182453.RAcKdy_oiRfZqy6z6V-9--T32_x4ifEIbyn3cVQvVuUtw130_provenance.
- NP182456.RAfs6koHvhGtrncTYMhrPQKlzNZHwnLxzGcumpcAp2KK8130_assertion description "[To compare the performance characteristics of prostate cancer risk factors such as total prostate-specific antigen (tPSA), percentage free PSA (%fPSA), PSA velocity (PSAV) and urinary prostate cancer gene 3 (PCA3) at first, second and ≥ third repeat biopsy session.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182456.RAfs6koHvhGtrncTYMhrPQKlzNZHwnLxzGcumpcAp2KK8130_provenance.
- NP182459.RAf54iiLaobQDs1n_sx319SygOL0xPagkQ1f2fSriyzPA130_assertion description "[MMP-2 mRNA was expressed in 26 of 28 oral squamous cell carcinoma (OSCC) specimens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182459.RAf54iiLaobQDs1n_sx319SygOL0xPagkQ1f2fSriyzPA130_provenance.
- NP182469.RATUv7h2jMtWSf4XgIik1MEDeWSUUl3N3dCDilO39Q4jQ130_assertion description "[In vivo, intravenous administration of an Ad-OC vector was effective against preexisting human prostate cancer subcutaneous and bone xenografts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182469.RATUv7h2jMtWSf4XgIik1MEDeWSUUl3N3dCDilO39Q4jQ130_provenance.
- NP182470.RAZdwl1iyzy7_8QbMsKEo9TtGnCveHxjSe23qSGLqr9Pw130_assertion description "[Data regarding cancer onset and death ages was obtained from our database and Statistical analysis was performed using the SPSS statistical package (SPCC Inc., Chicago, IL), and JMP software (SAS Institute, Cary, NC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182470.RAZdwl1iyzy7_8QbMsKEo9TtGnCveHxjSe23qSGLqr9Pw130_provenance.
- NP182476.RARlO6xdmCByAGJa_o1J3veWm5G8f_07d4QqWQ_zcyiXA130_assertion description "[CD7+ and CD56+ myeloid/natural killer cell precursor acute leukemia: a distinct hematolymphoid disease entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182476.RARlO6xdmCByAGJa_o1J3veWm5G8f_07d4QqWQ_zcyiXA130_provenance.
- NP182481.RAaK3MyOTHHh4GOweJ549jkSCBwADWRucf6cKjGTKkaAo130_assertion description "[In conclusion, although with the limitations of a small sample size and the few SNPs studied, this study demonstrates a lower frequency of VEGFR-2 rs2071559 AA genotype in an AMD patient population, suggesting future studies on the role VEGFR-2 SNPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182481.RAaK3MyOTHHh4GOweJ549jkSCBwADWRucf6cKjGTKkaAo130_provenance.
- NP182484.RAU5rCSsFuM39TmJkoefbg2xKTDHNAn1MWwszbwXIJE7s130_assertion description "[In the past decade, there have been major advances in our understanding of the molecular genetics and pathogenesis of obesity, especially with regards to the genetics and functions of chemical mediators and their receptors, such as leptin, the leptin receptor, neuropeptide Y, the melanocortin-4 receptor, agouti-related protein and the peroxisome-proliferator-activated receptor gamma 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182484.RAU5rCSsFuM39TmJkoefbg2xKTDHNAn1MWwszbwXIJE7s130_provenance.
- NP182489.RAUauQE853L00hnbQqH0V0zTwrPQTggy7zetyygn2q89o130_assertion description "[Levels of IL-1β (p = 0.001) and TNF-α (p = 0.01) were significantly elevated in H. pylori-positive GBC compared to the control group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182489.RAUauQE853L00hnbQqH0V0zTwrPQTggy7zetyygn2q89o130_provenance.
- NP182491.RAUHlxNMTHBybUR4bwyX8fJhvhSP998cQIpL-PkbPtRiU130_assertion description "[FOXO1 impairs whereas statin protects endothelial function in diabetes through reciprocal regulation of Kruppel-like factor 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182491.RAUHlxNMTHBybUR4bwyX8fJhvhSP998cQIpL-PkbPtRiU130_provenance.
- NP182492.RAUJa0X_gceC0cFtNjPoSvgwd6W5wV-I5KmS-UAul-MBs130_assertion description "[MSCs isolated from patients with BOS demonstrated increased expression of α-SMA and collagen I when compared with non-BOS controls, consistent with a stable in vivo fibrotic phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182492.RAUJa0X_gceC0cFtNjPoSvgwd6W5wV-I5KmS-UAul-MBs130_provenance.
- NP182493.RAVhPTTig6Eb5juyZT7GYUMGNkvV63cla833JuSdgSfPk130_assertion description "[COX2 overexpression has been detected in up to 90% of colon carcinomas, and its downregulation inhibits polyp formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182493.RAVhPTTig6Eb5juyZT7GYUMGNkvV63cla833JuSdgSfPk130_provenance.
- NP182495.RASbbykU6iToHTiCvXZijy6kmoByuELB8PWNikUhUtJkM130_assertion description "[In addition, a significant up-regulation of p15INK4B gene expression is observable during the development of the acute phase of malignancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182495.RASbbykU6iToHTiCvXZijy6kmoByuELB8PWNikUhUtJkM130_provenance.
- NP182496.RAfD9CBDNFr6eWMDc1aqq2Gia7uwfCJYBX4sTCwJ9RpB8130_assertion description "[The presence of COX-2 expression in PJS carcinomas and dysplastic hamartomas provides a rationale for chemoprevention with nonsteroidal anti-inflammatory drugs or COX-2 inhibitors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182496.RAfD9CBDNFr6eWMDc1aqq2Gia7uwfCJYBX4sTCwJ9RpB8130_provenance.
- NP182503.RAfpoYQrr6l5l3D58FlQI635nMrARg1A7RW8PE32fUkhs130_assertion description "[The abnormally spliced mRNA product from the alpha1-gene carrying the mutation does not lead to functional protein and causes a mild HbH-disease phenotype when in combination with the deletion type alpha0-thalassaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182503.RAfpoYQrr6l5l3D58FlQI635nMrARg1A7RW8PE32fUkhs130_provenance.
- NP182507.RAR1fbalFDuqm14oqt97kzi5KjV1wxQraAiutBKWYYbiI130_assertion description "[Resistin, specifically secreted from adipocytes, antagonizes insulin and represents a promising candidate gene for type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182507.RAR1fbalFDuqm14oqt97kzi5KjV1wxQraAiutBKWYYbiI130_provenance.
- NP182508.RASGdwDppTVvKPkFxxC564AU2smN0tV-kmPlYXTSB65Lg130_assertion description "[Together, with the low toxicity profile of PPAR-γ ligands, our data show that these ligands may serve as potential therapeutic agents to inhibit metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182508.RASGdwDppTVvKPkFxxC564AU2smN0tV-kmPlYXTSB65Lg130_provenance.
- NP182509.RAc9tBG44fC1wMozXclSEoqbbE-UJZKugzVt4wGCXDJ6k130_assertion description "[Polymorphic analysis of the human MHC-linked heat shock protein 70 (HSP70-2) and HSP70-Hom genes in insulin-dependent diabetes mellitus (IDDM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182509.RAc9tBG44fC1wMozXclSEoqbbE-UJZKugzVt4wGCXDJ6k130_provenance.
- NP182518.RAeiU7J6XZqQ1egj5J9WeSQCYrTB3EoUfZCe7MEQfX4bU130_assertion description "[Influence of Serum Amyloid A (SAA1) and SAA2 gene polymorphisms on renal amyloidosis, and on SAA/C-reactive protein values in patients with familial mediterranean fever in the Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182518.RAeiU7J6XZqQ1egj5J9WeSQCYrTB3EoUfZCe7MEQfX4bU130_provenance.
- NP182520.RAelHNw0HK-PymsnOA7QuAdayPXzX9p6HfIzLMYuT35iQ130_assertion description "[These data suggest a role of the NOS3 gene in the pathogenesis of metabolic syndrome in hypertensive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182520.RAelHNw0HK-PymsnOA7QuAdayPXzX9p6HfIzLMYuT35iQ130_provenance.
- NP182530.RAZ-xJomyUx0XXjFUwwHh5hBRQFKk0MyQpLi58L_qb0qY130_assertion description "[Flow cytometric analysis of estrogen, progesterone receptor expression and DNA content in formalin-fixed, paraffin-embedded human breast tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182530.RAZ-xJomyUx0XXjFUwwHh5hBRQFKk0MyQpLi58L_qb0qY130_provenance.
- NP182531.RASwtqXjiclI5rtiPbv6JVUWOCYTNLwONfKSMTzAYbjAo130_assertion description "[Microarray analysis of specific areas of cerebral cortex from individuals who had suffered from major depressive disorder demonstrated significant down-regulation of SLC1A2 and SLC1A3, two key members of the glutamate/neutral amino acid transporter protein family, SLC1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182531.RASwtqXjiclI5rtiPbv6JVUWOCYTNLwONfKSMTzAYbjAo130_provenance.
- NP182534.RAd796X4JCnPC8uSddAUtDcn_zl7km5z7BjwiPYWrVvWI130_assertion description "[To map shared and seizure type-related susceptibility loci, both nonparametric loci (NPL) and parametric linkage analyses were performed for a broad trait model (GGEs) in the entire set of GGE-multiplex families and a narrow trait model (typical absence or myoclonic seizures) in the subgroups of JME and GAE families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182534.RAd796X4JCnPC8uSddAUtDcn_zl7km5z7BjwiPYWrVvWI130_provenance.
- NP182537.RASJ9-I9fmfH1oa-UXKgS-Y9EJMxUup85q7ZFNii6712I130_assertion description "[This esophageal-cancer susceptibility locus, TOC (tylosis with oesophageal cancer), might be a target of deletions at 17q25.1 in multiple types of malignancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182537.RASJ9-I9fmfH1oa-UXKgS-Y9EJMxUup85q7ZFNii6712I130_provenance.
- NP182541.RAaxs0z5XVaVwHHQaJl9g_9BHSRimMUPh7iQstvzyKtoA130_assertion description "[Three loci for the restless legs syndrome (RLS) on chromosomes 12q, 14q, and 9p (RLS1, RLS2, and RLS3) have been mapped, but no gene has been identified as yet.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182541.RAaxs0z5XVaVwHHQaJl9g_9BHSRimMUPh7iQstvzyKtoA130_provenance.
- NP182549.RATs7WDsEDdRQ9tlkz8kTzC8YqWonCDwUqQ0G3o6stuyc130_assertion description "[Immunohistochemical expression of ERK-1 and ERK-2 in the squamous carcinomas was diffuse throughout the tumor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182549.RATs7WDsEDdRQ9tlkz8kTzC8YqWonCDwUqQ0G3o6stuyc130_provenance.
- NP182551.RAUqqgFQv1tIyxzDVxcUHlOux0L8ahQ-Z6hUzK8r6-PUg130_assertion description "[A cytomegaloviral vector containing the decorin transgene caused greatly reduced cell growth, motility and observed metastases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182551.RAUqqgFQv1tIyxzDVxcUHlOux0L8ahQ-Z6hUzK8r6-PUg130_provenance.
- NP182552.RAbNBFXWlZjMEE1yfsH9SpFJwa6eCvhdixqkktJg_s4Wc130_assertion description "[The high incidence of RET/PTC and Trk rearrangements or point mutations in RAS and c-MET oncogenes are the genetic hallmarks of PTC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182552.RAbNBFXWlZjMEE1yfsH9SpFJwa6eCvhdixqkktJg_s4Wc130_provenance.
- NP182567.RAZXheMq72FLLQ7j2v4TTPzDrYn2dHo6P5uFE7sbaQ5aw130_assertion description "[COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182567.RAZXheMq72FLLQ7j2v4TTPzDrYn2dHo6P5uFE7sbaQ5aw130_provenance.
- NP182568.RAY8xW5AchF0P5UU2G2NuZkO0nd6IHUAlkCy9zrAT1HMY130_assertion description "[Male sex, PKD1 gene, episodes of gross hematuria, and the precocity and severity of hypertension play an important role in the progression of renal disease to ESRF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182568.RAY8xW5AchF0P5UU2G2NuZkO0nd6IHUAlkCy9zrAT1HMY130_provenance.
- NP182569.RARc-fQ0A7kQDHDVwbiZ-w2b8swVkc1kSorOjn-2whWOg130_assertion description "[Disease activity measured using the SLEDAI-2K is correlated with the high IFN gene signature, indicating that GEP may be a useful biomarker of disease activity in SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182569.RARc-fQ0A7kQDHDVwbiZ-w2b8swVkc1kSorOjn-2whWOg130_provenance.
- NP182571.RAcHpYPXNRXkYnhVKUIMueWF7TCcMcOvvPf8l11T7xKyA130_assertion description "[Vesicular monoamine transporter subtype 2 (VMAT2) activity protects against neurotoxins, and reduced VMAT2 expression is implicated in drug addiction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182571.RAcHpYPXNRXkYnhVKUIMueWF7TCcMcOvvPf8l11T7xKyA130_provenance.
- NP182577.RAfOLdeZO2cDfQG6-KOXwS-MZW9bQAcgimMSNNnMpOgmc130_assertion description "[Although sophisticated analytical methods have yielded comprehensive data about the conformation of the native protein both as a monomer and as the light chain of the type I major histocompatibility complex, the cause and mechanisms leading to the transformation of beta(2)m into amyloid deposits in patients with dialysis-related amyloidosis are unsettled.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182577.RAfOLdeZO2cDfQG6-KOXwS-MZW9bQAcgimMSNNnMpOgmc130_provenance.
- NP182584.RAWfLH3mkh3mtBQbKHDkX9H_mmfbVef3RGXSkeyq_IspI130_assertion description "[The INS-GAS mouse, a transgenic mouse model of gastric carcinogenesis which overexpresses amidated gastrin, was used to investigate the in vivo relationship between HB-EGF, MMP-7, gastrin and EMT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182584.RAWfLH3mkh3mtBQbKHDkX9H_mmfbVef3RGXSkeyq_IspI130_provenance.
- NP182585.RAfya6AwfzC5cl-0EDNyMUaT8_T7RKYT8MR1XHtp9ANpo130_assertion description "[Clinical implications of expression of ETS-1 in relation to angiogenesis in ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182585.RAfya6AwfzC5cl-0EDNyMUaT8_T7RKYT8MR1XHtp9ANpo130_provenance.
- NP182588.RAa5dUXMrOz_EVsaGLn5EkLsFthz4rIbXJdWuTrj0hdyw130_assertion description "[Among the proteins associated with the malignant phenotype, Gamma-glutamyl hydrolase, CD44, Galectin-3-binding protein, and Syndecan-1 protein have been reported as potential biomarkers of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182588.RAa5dUXMrOz_EVsaGLn5EkLsFthz4rIbXJdWuTrj0hdyw130_provenance.
- NP182589.RAaL_MPm6N8gJlBVa_8oJaI9-DJcFAPsT5cp3ejv8pkyE130_assertion description "[Pharmacologic inhibitors of the prostaglandin-synthesizing COX-2 oncogene prevent the development of premalignant human colon adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182589.RAaL_MPm6N8gJlBVa_8oJaI9-DJcFAPsT5cp3ejv8pkyE130_provenance.
- NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_assertion description "[To determine whether there are any molecular markers that might help explain this paradox between pathologically aggressive neoplasms in patients with HBC and the lack of extreme clinically aggressive disease, we studied several molecular parameters in a group of 34 breast cancer patients with mutations in either the BRCA1 or BRCA2 tumor suppressor genes and compared them with a group of 20 breast cancer patients with non-HBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182591.RAZUbn-uUjuLztw6bRSXFXAf1mJPRXK5T6cn8WgHoipho130_provenance.
- NP182592.RASqzkAIz78j8fnI43oaVtrnXdK8Rrq_xD6zniQcq95oo130_assertion description "[Previous allelic deletion studies in enteropancreatic ETs suggested MEN1 gene involvement in tumorigenesis of familial pancreatic ETs (nongastrinomas) and sporadic gastrinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182592.RASqzkAIz78j8fnI43oaVtrnXdK8Rrq_xD6zniQcq95oo130_provenance.
- NP182593.RAQ68Wxl29s17Bu0HnhQLS40UciM0FaEbgAsSh8ZihxQw130_assertion description "[MCT8 mutations usually cause abnormal thyroid function in addition to neurological abnormalities, but this proband had normal thyroid function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182593.RAQ68Wxl29s17Bu0HnhQLS40UciM0FaEbgAsSh8ZihxQw130_provenance.
- NP182597.RAcU1uRYC46TH7SO0m1FxZoyOPwTbGG7VZgx-djEs1OgI130_assertion description "[We investigated the association between a null mutation in the ciliary neurotrophic factor (CNTF) gene and functional psychoses including schizophrenia and schizoaffective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182597.RAcU1uRYC46TH7SO0m1FxZoyOPwTbGG7VZgx-djEs1OgI130_provenance.
- NP182598.RAeTAUiaq-nVu9cftRTJGOhhZNYg_SgTgxU9kjO9GuMDk130_assertion description "[The ACE rs4291 TT genotype, which has been associated with HPA axis hyperactivity and higher levels of serum angiotensin converting enzyme (ACE), predicted acute stress response and reports of physician-diagnosed CVD in a national sample following collective stress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182598.RAeTAUiaq-nVu9cftRTJGOhhZNYg_SgTgxU9kjO9GuMDk130_provenance.
- NP182600.RAZm7JzuVdSE_Z2J2JgTm7i2wCd3BdUvmDWYxzsn3e4n8130_assertion description "[We have identified a novel gene MEL1 (MDS1/EVI1-like gene 1) encoding a zinc finger protein near the breakpoint of t(1; 3)(p36;q21)-positive human acute myeloid leukemia (AML) cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182600.RAZm7JzuVdSE_Z2J2JgTm7i2wCd3BdUvmDWYxzsn3e4n8130_provenance.
- NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_assertion description "[Linkage analyses in experimental crosses of stroke-prone spontaneously hypertensive (SHRSP) and normotensive Wistar-Kyoto (WKY) rats have strongly suggested the presence of quantitative trait loci (QTL) influencing blood pressure and ACE levels on rat chromosome 10, which have been confirmed in multiple independent studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182609.RAfsfrrLQPcYvett3OggVNo_tQnU4S9zGmRw2BEBLJHYg130_provenance.
- NP182612.RAfJkXUh19ARU7C4ibsB-woqgope-gPN5Z12EQrtDTaQo130_assertion description "[HHV-8 DNA was detected in 3 CBS and 6 peripheral blood samples from 11 HHV-8-seropositive women but not in CBS from 78 seronegative women, 96 women from the colposcopy clinic, or in blood samples from 82 seronegative women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182612.RAfJkXUh19ARU7C4ibsB-woqgope-gPN5Z12EQrtDTaQo130_provenance.
- NP182614.RAdSP1pZrrxyRPWA2ucyxjHm5jcsmTvlNxG8t4sV6ANDw130_assertion description "[PMSG was applied to the RDS/peripherin gene of 16 individuals from a family exhibiting autosomal dominant macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182614.RAdSP1pZrrxyRPWA2ucyxjHm5jcsmTvlNxG8t4sV6ANDw130_provenance.
- NP182617.RARQNBQW1ygTg0yqGND35QtEAWB6Fx_qBJbYP9pYsm4gc130_assertion description "[Sections of parathyroid adenomas from 12 cases were stained using PCNA (proliferating cell nuclear antigen), EGFR, and p53 immunohistochemistry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182617.RARQNBQW1ygTg0yqGND35QtEAWB6Fx_qBJbYP9pYsm4gc130_provenance.
- NP182618.RAVXrEIIOIXdwuv6bmL9CH3cmpwh2nddxGtIdOUI71ouY130_assertion description "[The relative amounts of plasma transthyretin forms in familial transthyretin amyloidosis: a quantitative analysis by Fourier transform ion-cyclotron resonance mass spectrometry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182618.RAVXrEIIOIXdwuv6bmL9CH3cmpwh2nddxGtIdOUI71ouY130_provenance.
- NP182626.RAZcjvOzwM2UbnhCtUGxahcMD3SVewtSRGbgYZToFmdhY130_assertion description "[Melanoma candidate genes CDKN2A/p16/INK4A, p14ARF, and CDK4 sequencing in patients with uveal melanoma with relative high-risk for hereditary cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182626.RAZcjvOzwM2UbnhCtUGxahcMD3SVewtSRGbgYZToFmdhY130_provenance.
- NP182628.RAZ9Xl8Lw-PPEZsWpLZxo3AXFkF4fYprvUI3aUQ5DjXnQ130_assertion description "[Our results demonstrate that both TLR2 and TLR4 signalling are critical to the regulation of infection in non-typeable H. influenzae-induced otitis media.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182628.RAZ9Xl8Lw-PPEZsWpLZxo3AXFkF4fYprvUI3aUQ5DjXnQ130_provenance.
- NP182629.RAXYF3vEdYOGkSOWySPfrm7GXGkIC576pM9SXa5U0CMgs130_assertion description "[Here we examined circulating concentrations of inflammatory cytokines (IFN-γ, TNF-α, IL-1β, IL-6), and the acute phase protein CRP alongside plasma tryptophan, kynurenine, kynurenic acid (KYNA) and 3-hydroxyanthranilic acid (3-HAA) concentrations, and whole blood mRNA expression of IDO, kynurenine aminotransferases (KAT I and II), kynurenine-3-monooxygenase (KMO), kynureninase and SERT in patients with major depressive disorder (MDD) compared with age and sex-matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182629.RAXYF3vEdYOGkSOWySPfrm7GXGkIC576pM9SXa5U0CMgs130_provenance.
- NP182634.RAXfQmyq5gJF2eCh-TAhtmwJVLC3Eoq2bTft0vFO1GTWU130_assertion description "[We reviewed cases of HI with sexual precocity reported in the literature and focused on collecting information on other associated organ abnormalities, chromosomal karyotype, and type of sexual precocity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182634.RAXfQmyq5gJF2eCh-TAhtmwJVLC3Eoq2bTft0vFO1GTWU130_provenance.
- NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_assertion description "[Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182635.RATGy6qHpceYzbCy16s1o6Srt6SlYP6IxcF9_IJsWpxFE130_provenance.
- NP182638.RATo2Jx-uP7TyN39RLcSM3Zkm3fon51Iq_6cNtLQzq-gU130_assertion description "[A unique opportunity to study the pathogenesis of human autoimmunity is provided by autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), a rare inherited autoimmune disease caused by mutations in Autoimmune Regulator (AIRE) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182638.RATo2Jx-uP7TyN39RLcSM3Zkm3fon51Iq_6cNtLQzq-gU130_provenance.
- NP182644.RAav-qJLVUzA0IAhogxua8XYVZnDXuyucFOb_IyZgIN-I130_assertion description "[We observed that GSTM1 null genotype was present in 46.74% of the ESRD patients while GSTT1 null genotype was present in 58.7% of the ESRD subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182644.RAav-qJLVUzA0IAhogxua8XYVZnDXuyucFOb_IyZgIN-I130_provenance.
- NP182645.RAWwnnl0X8xbGEPnEqsyXihpnOQTgA-CfyIb2OJ7VZ0LE130_assertion description "[Lys656Asn polymorphism of LEPR gene is associated with obesity parameters, insulin resistance and glucose levels in patients with NAFLD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182645.RAWwnnl0X8xbGEPnEqsyXihpnOQTgA-CfyIb2OJ7VZ0LE130_provenance.
- NP182647.RAQTwstnXwNSWFH2tKaLw2oX8oEklTMaP8BS0aGTa8x7U130_assertion description "[These studies suggest that altM-CSF may be a tumor antigen for HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182647.RAQTwstnXwNSWFH2tKaLw2oX8oEklTMaP8BS0aGTa8x7U130_provenance.
- NP182648.RAUBT4igwo31mVWSsEobA_ERc4R93MYmGAjFZO0x5BF6M130_assertion description "[In conclusion, these findings indicate that up-regulation of DDR1 may contribute to the progression and poor prognosis of NSCLC and this effect may be associated with increased invasiveness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182648.RAUBT4igwo31mVWSsEobA_ERc4R93MYmGAjFZO0x5BF6M130_provenance.
- NP182650.RARVI2o_eWwXkNPviXKDz847XuG8LgJXZV6p12hnq5Og0130_assertion description "[The low level of RUNX3 expression in gastric epithelium and the absence of downregulation in gastric cancer do not support the hypothesis that RUNX3 functions as a gastric tumour suppressor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182650.RARVI2o_eWwXkNPviXKDz847XuG8LgJXZV6p12hnq5Og0130_provenance.
- NP182657.RAWvL94js_t03diBImpONugNlovUQUl1xSWoUkVeIrn4o130_assertion description "[HLA-DQA1 and HLA-DQB1 genes may jointly determine susceptibility to develop multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182657.RAWvL94js_t03diBImpONugNlovUQUl1xSWoUkVeIrn4o130_provenance.
- NP182658.RARUCDnMVJGgXpDuTFthhXhp0ls1uLsz-9p2mUHMxlSSc130_assertion description "[hairpins or G-quadruplex structures) may serve as endogenous, invasion-inducing TLR9-ligands and promote local progression and metastasis of cancers in the alimentary tract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182658.RARUCDnMVJGgXpDuTFthhXhp0ls1uLsz-9p2mUHMxlSSc130_provenance.
- NP182660.RAdmplJW6eDCPS6wYZZXxfUx3yuyjPQAxMcENjK4zeTVo130_assertion description "[Our findings provide new insights into the mechanisms of acquired resistance to 5-FU in colorectal cancer and implicate UMPK as an important mechanism of clinical resistance to pulse 5-FU treatment in some patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182660.RAdmplJW6eDCPS6wYZZXxfUx3yuyjPQAxMcENjK4zeTVo130_provenance.
- NP182668.RASTxofDSHWNdPXG-cnLM0zcPOGCcv1wt0HBO4K5fhhsg130_assertion description "[Codons R124 and R555 of the BIGH3 gene represent mutational hotspots in the genomes of Japanese patients with autosomal-dominant CD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182668.RASTxofDSHWNdPXG-cnLM0zcPOGCcv1wt0HBO4K5fhhsg130_provenance.
- NP182669.RAXuA3VaImGllLHRm0cWu3Bd67XXLw2-e0JmpoJo7yffU130_assertion description "[The most frequent genetic alterations are deletions in 13q14, 17p13 (TP53) and 11q22-q23 (ATM), and trisomy of chromosome 12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182669.RAXuA3VaImGllLHRm0cWu3Bd67XXLw2-e0JmpoJo7yffU130_provenance.
- NP182674.RAZrTIQE1glfvZRfZ-JVUI6_3MlT3ljflRyQ2wGfsObME130_assertion description "[These data suggest that the GC 2 allele exerts a protective effect, whereas 1F, when homozygous, increases the risk of developing COAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182674.RAZrTIQE1glfvZRfZ-JVUI6_3MlT3ljflRyQ2wGfsObME130_provenance.
- NP182675.RAVPzHeYEQya_1d7AgmB8nOg2RUVmuOILcjZY1jp-xwfs130_assertion description "[To analyze the clonality of T cell receptor (TCR) V beta 2- and V beta 13-positive T cells, which are predominantly expressed in the lips of patients with Sjögren's syndrome (SS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182675.RAVPzHeYEQya_1d7AgmB8nOg2RUVmuOILcjZY1jp-xwfs130_provenance.
- NP182677.RATx77_9vcGlxGqlMV8chqPO2poYb5FA5XipWQsDoarCE130_assertion description "[KRAS rearrangement may represent the driving mutation in a rare subset of metastatic prostate cancers, emphasizing the importance of RAS-RAF-MAPK signaling in this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182677.RATx77_9vcGlxGqlMV8chqPO2poYb5FA5XipWQsDoarCE130_provenance.