Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP43554.RAihFbGttjH3GjkjjFGl2X4T3qW2YIbVGJaMxfLzJZn4I130_assertion description "[Del(GJB6-D13S1830) and GJB2/del(GJB6-D13S1830) mutations have been shown to be the second most frequent cause of deafness in different populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43554.RAihFbGttjH3GjkjjFGl2X4T3qW2YIbVGJaMxfLzJZn4I130_provenance.
- NP43556.RAvXH4qPuMd5xBumNIBSDa-EhapTUbnqOVP35WUx3mnW0130_assertion description "[GJB2 mutation is a major cause for NSHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43556.RAvXH4qPuMd5xBumNIBSDa-EhapTUbnqOVP35WUx3mnW0130_provenance.
- NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_assertion description "[Most probands have a congenital HL that is stable, symmetrical and without associated manifestations, but the audiometric profile should not be the only criteria for offering mutational screening of DFNB1 because of the observed variability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_provenance.
- NP43578.RAjwEJYGIcfLg_4Qoey5PX4yx2edqmZ7MSRFz446ZPmk8130_assertion description "[The CMT1Adup, GJB1, MPZ and PMP22 mutation frequencies were in the range of those described in other CMT patient collectives with different ethnical backgrounds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43578.RAjwEJYGIcfLg_4Qoey5PX4yx2edqmZ7MSRFz446ZPmk8130_provenance.
- NP43579.RAqIXFmGsujRgTkLrRz37KadbVvM40TE3ZIyiaK9G8Lhk130_assertion description "[Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43579.RAqIXFmGsujRgTkLrRz37KadbVvM40TE3ZIyiaK9G8Lhk130_provenance.
- NP43584.RAieFdnlnznTqBU_byHWdhS-gVDzAG0uniGN9ATrc-V3o130_assertion description "[The findings expand the spectrum of mutations in connexin40 linked to AF and provide new insight into the molecular aetiology involved in the pathogenesis of AF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43584.RAieFdnlnznTqBU_byHWdhS-gVDzAG0uniGN9ATrc-V3o130_provenance.
- NP43589.RAj_0xGA2cf9dfyOfqR709GtDfeSUJVimZCEYkHX7IKpk130_assertion description "[Association between C1019T polymorphism of connexin37 and acute myocardial infarction: a study in patients from Sicily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43589.RAj_0xGA2cf9dfyOfqR709GtDfeSUJVimZCEYkHX7IKpk130_provenance.
- NP43594.RAuPE99-JClqyfBPmSEF_IGDivbTYjzCCTWZq2wc7tojg130_assertion description "[Further studies are needed to explore contributions from other genetic factors such as rare variants in these genes and variation outside of these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43594.RAuPE99-JClqyfBPmSEF_IGDivbTYjzCCTWZq2wc7tojg130_provenance.
- NP43596.RAiFShLkZiVRrKCKy6Dh6XZnli9Wz8e0dtAbs-Pq0JNLI130_assertion description "[Polymorphisms in genes involved in GH1 release and their association with breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43596.RAiFShLkZiVRrKCKy6Dh6XZnli9Wz8e0dtAbs-Pq0JNLI130_provenance.
- NP43598.RApLmNRJ-0vuQkso8T9SVlhUPKF1s-dHtyuknnza49lxw130_assertion description "[ It is suggested that the SNP of GHR are unevenly distributed and different in different ethnic populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43598.RApLmNRJ-0vuQkso8T9SVlhUPKF1s-dHtyuknnza49lxw130_provenance.
- NP43600.RAgUVXqhvDR7FpsdLlrZukLafF0G4jpQMnDZmMTRsReRQ130_assertion description "[Genetic variation in the growth hormone synthesis pathway in relation to circulating insulin-like growth factor-I, insulin-like growth factor binding protein-3, and breast cancer risk: results from the European prospective investigation into cancer and nutrition study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43600.RAgUVXqhvDR7FpsdLlrZukLafF0G4jpQMnDZmMTRsReRQ130_provenance.
- NP43607.RAtJeORgogrwEucbV3I8e8ChXiafxzzCszns2AGIlHtrY130_assertion description "[Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43607.RAtJeORgogrwEucbV3I8e8ChXiafxzzCszns2AGIlHtrY130_provenance.
- NP43610.RAnfrZnNsEylY-RJF9Nwq0z2lBau0escnq6aooTXv0RVo130_assertion description "[The influence of sequence variations in factor VII, gamma-glutamyl carboxylase and vitamin K epoxide reductase complex genes on warfarin dose requirement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43610.RAnfrZnNsEylY-RJF9Nwq0z2lBau0escnq6aooTXv0RVo130_provenance.
- NP43617.RAvnY3VSZj9MJEQaGvJPpAgK83jz5P9esFYPOVBN8fVyo130_assertion description "[Overall, we obtained no solid evidence for the involvement of the GDNF gene in the pathogenesis of schizophrenia, although further studies in larger numbers of subjects will be required to conclude whether the trinucleotide repeat polymorphism is associated with the development of schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43617.RAvnY3VSZj9MJEQaGvJPpAgK83jz5P9esFYPOVBN8fVyo130_provenance.
- NP43620.RAtS_ObwOPEaYfGWAA_ArkKdR2TbHPzW2cpcSBE4k2FOA130_assertion description "[ This study identifies a strong association between MIC-1 serum levels and neoplastic progression within the large bowel. We suggest that the measurement of serum MIC-1 levels and determination of MIC-1 genotype may have clinical use in the management of patients with CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43620.RAtS_ObwOPEaYfGWAA_ArkKdR2TbHPzW2cpcSBE4k2FOA130_provenance.
- NP43623.RAlL8NpFNyOyMg-ID0sOt81uA14RBjbWjETZxdJ4_pHPQ130_assertion description "[The minor -588T allele of polymorphism -588C/T of a modifier subunit gene in glutamate-cysteine ligase (GCLM), a rate-limiting enzyme for glutathione (GSH) synthesis, was associated with lower plasma GSH levels and was a risk factor for myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43623.RAlL8NpFNyOyMg-ID0sOt81uA14RBjbWjETZxdJ4_pHPQ130_provenance.
- NP43624.RArA8g2F8Jdnrt-FQUZddkFMO1e4YHXQKgvMT82uO6zcw130_assertion description "[The molecular genetics of the human I locus and molecular background explain the partial association of the adult i phenotype with congenital cataracts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43624.RArA8g2F8Jdnrt-FQUZddkFMO1e4YHXQKgvMT82uO6zcw130_provenance.
- NP43628.RAoluf_btj8Tb83FbbHcA_DElTJxA2MSKDabySNFf43Tc130_assertion description "[ The -30G-->A polymorphism of the beta-cell-specific promoter of GCK and the I27L polymorphism of HNF1A seem to increase the risk of GDM in Scandinavian women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43628.RAoluf_btj8Tb83FbbHcA_DElTJxA2MSKDabySNFf43Tc130_provenance.
- NP43631.RAs_xQhB1yMfNHl7oONQcnS4xnbjXsSIyXmMu3hz6thnM130_assertion description "[Our research suggested in Chinese population the prevalences of MODY2 was less than 1% in early onset familial type 2 diabetic patients, the IVS9+8 C>T polymorphism at MODY2 gene, intron 9 or nearby genes was associated with early onset familial type 2 diabetes .]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43631.RAs_xQhB1yMfNHl7oONQcnS4xnbjXsSIyXmMu3hz6thnM130_provenance.
- NP43634.RAi_4P9pPZgAvVkJ6vSVLKMbFBrA0HTcj2fD1hvFd8_M0130_assertion description "[Linkage analysis does not support a role for glucokinase gene in the aetiology of type 2 diabetes mellitus among north western Italians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43634.RAi_4P9pPZgAvVkJ6vSVLKMbFBrA0HTcj2fD1hvFd8_M0130_provenance.
- NP43650.RAlW-9XWhUN4v7NYvbnHf7P02utRxXtZzgO14TRKQD2E8130_assertion description "[Human glucagon-like peptide-1 receptor gene in NIDDM. Identification and use of simple sequence repeat polymorphisms in genetic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43650.RAlW-9XWhUN4v7NYvbnHf7P02utRxXtZzgO14TRKQD2E8130_provenance.
- NP43651.RAp6RsvYz19HkZmukEbLQMClrUUmzy3JW0Fyk71yY8ck4130_assertion description "[A population association study of four candidate genes (hexokinase II, glucagon-like peptide-1 receptor, fatty acid binding protein-2, and apolipoprotein C-II) with type 2 diabetes and impaired glucose tolerance in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43651.RAp6RsvYz19HkZmukEbLQMClrUUmzy3JW0Fyk71yY8ck4130_provenance.
- NP43663.RAmWZZqEUqdH0xZQVGo_849Y_FM1Jo4XD4838EjJzrmdU130_assertion description "[The aim of this study was to characterise the GBA mutations and analyze genotype/phenotype relationships in 193 unrelated patients from the Spanish GD Registry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43663.RAmWZZqEUqdH0xZQVGo_849Y_FM1Jo4XD4838EjJzrmdU130_provenance.
- NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_assertion description "[To characterize sequence variation within the glucocerebrosidase (GBA) gene in a select subset of our sample of patients with familial Parkinson disease (PD) and then to test in our full sample whether these sequence variants increased the risk for PD and were associated with an earlier onset of disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_provenance.
- NP43677.RAi7jZHwW-_BVMDQ_f38NuTERijFzTeutiqlqnKAntpzo130_assertion description "[The frequency of GBA mutations among the Chinese PD probands was 4.3%, in contrast to 1.1% in Chinese controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43677.RAi7jZHwW-_BVMDQ_f38NuTERijFzTeutiqlqnKAntpzo130_provenance.
- NP43681.RAjP4a1H-wVd2vUrvV-YwnT9aFm758eUwF7gzF1DEdYgU130_assertion description "[We screened this gene in 46 patients with essential thrombocythemia and identified only a common single nucleotide polymorphism that is unlikely to be of pathological significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43681.RAjP4a1H-wVd2vUrvV-YwnT9aFm758eUwF7gzF1DEdYgU130_provenance.
- NP43682.RAq27cne3Kdrq19vZCwEZiA9eU2mTXQIr_RfXakzQv_ig130_assertion description "[ We identified a panel of novel SNPs in genes coding for proteins important in the T H 1/T H 2 cell differentiation. SNPs of the GATA3 gene showed an initial association to asthma-related phenotypes. Elucidation of the importance of the identified panel of SNPs in other T H 1/T H 2 mediated diseases will be of great interest.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43682.RAq27cne3Kdrq19vZCwEZiA9eU2mTXQIr_RfXakzQv_ig130_provenance.
- NP43695.RAhLREZopDckSpeUlkz7Fd2w5aCqcnaXFi813_hsCcRpc130_assertion description "[This study did not support the hypothesis that reduced galactose metabolism is a risk factor for ovarian cancer, although increased GALT activity attenuated the inverse association of oral contraceptive pill use with risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43695.RAhLREZopDckSpeUlkz7Fd2w5aCqcnaXFi813_hsCcRpc130_provenance.
- NP43697.RArD0s2qFO8BPOX5thUbnei76J_tKWYlTjb4HWM8_yOpM130_assertion description "[No significant differences in allele frequency were detected between the Traveller and non-Traveller groups, or between the Irish population groups and the literature values for Northern and Western Europe.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43697.RArD0s2qFO8BPOX5thUbnei76J_tKWYlTjb4HWM8_yOpM130_provenance.
- NP43699.RAr3YZ-_ie5H47IOOng0JDwuV61WYkvFi3ROmUGlKr0So130_assertion description "[The P28T mutation in the GALK1 gene accounts for galactokinase deficiency in Roma (Gypsy) patients across Europe.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43699.RAr3YZ-_ie5H47IOOng0JDwuV61WYkvFi3ROmUGlKr0So130_provenance.
- NP43700.RAombry3-jUPZTmxch0IV2Di_YkXZVAcOccjDmIU1_Yu0130_assertion description "[Galactokinase (GALK) deficiency is an autosomal recessive disorder characterized by hypergalactosemia and cataract formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43700.RAombry3-jUPZTmxch0IV2Di_YkXZVAcOccjDmIU1_Yu0130_provenance.
- NP43703.RAh8G31pWrHkt9XPtxOoVZee8yAz-zvntiJqkUJef66Ug130_assertion description "[A population-based association study of candidate genes for depression and sleep disturbance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43703.RAh8G31pWrHkt9XPtxOoVZee8yAz-zvntiJqkUJef66Ug130_provenance.
- NP43704.RAljC_Jk7_UPzM96zO56zCxUMGZhNPWR1pdT2vHXB1SsI130_assertion description "[ These analyses suggest that GABRG3 may be involved in the risk for alcohol dependence. These findings support the theory that the predisposition to alcoholism may be inherited as a general state of central nervous system disinhibition/hyperexcitability that results from an altered responsiveness to GABA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43704.RAljC_Jk7_UPzM96zO56zCxUMGZhNPWR1pdT2vHXB1SsI130_provenance.
- NP43709.RAkQiyfz2j-kff4XHjwnb4oo90ofl8SIq_JK59ZSHjjYo130_assertion description "[These LD findings, together with the association results, suggest that the GABRA6 and GABRA1 genes account for alcohol susceptibility in Han and exert their genetic influences in a somewhat dominant and synergistic fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43709.RAkQiyfz2j-kff4XHjwnb4oo90ofl8SIq_JK59ZSHjjYo130_provenance.
- NP43726.RAt9XYKD6VJ6nY70RTDPK1FAOGnXxhn3yj_dNq-tNYp2c130_assertion description "[Association study of dopamine D2, D4 receptor gene, GABAA receptor beta subunit gene, serotonin transporter gene polymorphism with children of alcoholics in Korea: a preliminary study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43726.RAt9XYKD6VJ6nY70RTDPK1FAOGnXxhn3yj_dNq-tNYp2c130_provenance.
- NP43733.RApFHcRa46vFG_bdzlW33wYCDQsWssFRS71jrW8wifDLI130_assertion description "[Association of GABRB3 polymorphisms with autism spectrum disorders in Korean trios.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43733.RApFHcRa46vFG_bdzlW33wYCDQsWssFRS71jrW8wifDLI130_provenance.
- NP43739.RAtqgvopQ4q1F3LST6py8hA90sXMXPdB2j7RaiQ1nJR_8130_assertion description "[Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43739.RAtqgvopQ4q1F3LST6py8hA90sXMXPdB2j7RaiQ1nJR_8130_provenance.
- NP43742.RAvsZ_wT0SasC_1bM5_J9M41dqHIGaujMSEx_Nsf0FOsA130_assertion description "[Systematic study of association of four GABAergic genes: glutamic acid decarboxylase 1 gene, glutamic acid decarboxylase 2 gene, GABA(B) receptor 1 gene and GABA(A) receptor subunit beta2 gene, with schizophrenia using a universal DNA microarray.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43742.RAvsZ_wT0SasC_1bM5_J9M41dqHIGaujMSEx_Nsf0FOsA130_provenance.
- NP43746.RApVaHBXkjir5atcKmPsVv3aFAlvZqzk4NP-eaXLDd7Xg130_assertion description "[Lack of GABABR1 gene variation (G1465A) in a Chinese population with temporal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43746.RApVaHBXkjir5atcKmPsVv3aFAlvZqzk4NP-eaXLDd7Xg130_provenance.
- NP43749.RAkO-zToGtD-4dVOg0dVMRS_Mw3fpqGtVepdC--C-YxVE130_assertion description "[There was no indication of an increased vulnerability to panic disorder or agoraphobia with respect to the allelic variants under study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43749.RAkO-zToGtD-4dVOg0dVMRS_Mw3fpqGtVepdC--C-YxVE130_provenance.
- NP43760.RAg78hYHVBCeh0ckw7SR5UgvQumUDYx6PuW9LXhHZCsl4130_assertion description "[These results suggest that the GABRA5 gene may confer susceptibility to bipolar I disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43760.RAg78hYHVBCeh0ckw7SR5UgvQumUDYx6PuW9LXhHZCsl4130_provenance.
- NP43767.RAvRnnFjZPNIpaXmc1Pyq--ugk3HDr22TL4LhioyA5e_I130_assertion description "[Positive association between the GABRA5 gene and unipolar recurrent major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43767.RAvRnnFjZPNIpaXmc1Pyq--ugk3HDr22TL4LhioyA5e_I130_provenance.
- NP43770.RAqKgj5uAA2VUJx3Ipyhc37CfFkksqtG1KfeMfFcj2JG4130_assertion description "[Previous studies in our lab indicated association of noncoding single nucleotide polymorphisms (SNPs) within a GABA receptor subunit gene on chromosome 4, GABRA4, and interaction between SNPs in GABRA4 and GABRB1 (also on chromosome 4), within Caucasian autism patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43770.RAqKgj5uAA2VUJx3Ipyhc37CfFkksqtG1KfeMfFcj2JG4130_provenance.
- NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_assertion description "[We conclude that GABRA4 is involved in the etiology of autism and potentially increases autism risk through interaction with GABRB1. These results support the hypothesis that GABA receptor subunit genes are involved in autism, most likely via complex gene-gene interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_provenance.
- NP43777.RAoXpdzjkG7V3cK2_RUlP9qS8whoSU86TrsnP_HnIThJA130_assertion description "[There was evidence of association to alcohol dependence for seven adjacent markers spanning 98,000 bp in the middle and 3'-portion of the GABRA2 gene (range of P-values = 0.008-0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43777.RAoXpdzjkG7V3cK2_RUlP9qS8whoSU86TrsnP_HnIThJA130_provenance.
- NP43779.RAp3-BnrGERiXKYVO6NYVgAbOFiWf-1fx9a0JUhPMjmNU130_assertion description "[The very strong association of GABRA2 with both alcohol dependence and the beta frequency of the electroencephalogram, combined with biological evidence for a role of this gene in both phenotypes, suggest that GABRA2 might influence susceptibility to alcohol dependence by modulating the level of neural excitation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43779.RAp3-BnrGERiXKYVO6NYVgAbOFiWf-1fx9a0JUhPMjmNU130_provenance.
- NP43782.RAv9veslWutBtdEm1JhsKkp-KPfnW_RblwCjW82sQQkhE130_assertion description "[These analyses provide evidence of both gene-environment correlation and gene-environment interaction associated with GABRA2, marital status, and alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43782.RAv9veslWutBtdEm1JhsKkp-KPfnW_RblwCjW82sQQkhE130_provenance.
- NP43784.RAnQ2No2S94LBkWvrdu0K2wg4LTZRBHnIKxmMy8vbSCY8130_assertion description "[First, we tested whether a single nucleotide polymorphism within GABRA2 gene, which encodes a subunit of the GABA(A) receptor, and that has been associated with AD, influences 'extreme' alcohol intake and second, the efficacy of three psychotherapies for alcoholism in treating extreme drinking behavior.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43784.RAnQ2No2S94LBkWvrdu0K2wg4LTZRBHnIKxmMy8vbSCY8130_provenance.
- NP43791.RAqt4v55TOn9vhl7aynyEPaPdlUUnWnQwPCB_KnHy6og0130_assertion description "[A pilot multivariate parallel ICA study to investigate differential linkage between neural networks and genetic profiles in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43791.RAqt4v55TOn9vhl7aynyEPaPdlUUnWnQwPCB_KnHy6og0130_provenance.
- NP43793.RAr0QLHgXzrqkOZs_HHAnSlTj5ozLqeCaMDojRO6giVFY130_assertion description "[We found evidence for association between GABRA1 and COGA alcohol dependence, history of blackouts, age at first drunkenness, and level of response to alcohol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43793.RAr0QLHgXzrqkOZs_HHAnSlTj5ozLqeCaMDojRO6giVFY130_provenance.
- NP43796.RAt90kbrhCfo7QKSnM7Oa-PC7bzLmeNdISE1HOyAG97Q8130_assertion description "[ These results indicate that the GABRA1 gene may play a role in the etiology of bipolar disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43796.RAt90kbrhCfo7QKSnM7Oa-PC7bzLmeNdISE1HOyAG97Q8130_provenance.
- NP43800.RAoC8dP8AeD25Dtb6s_V6R_Q3qfKWxz4wt-gD62nspR0s130_assertion description "[Possible association between the gamma-aminobutyric acid type B receptor 1 (GABBR1) gene and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43800.RAoC8dP8AeD25Dtb6s_V6R_Q3qfKWxz4wt-gD62nspR0s130_provenance.
- NP43806.RApr7AFstkH-EOqJtXwQGGPCGhP6zad6w59Sko_26IhI8130_assertion description "[Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43806.RApr7AFstkH-EOqJtXwQGGPCGhP6zad6w59Sko_26IhI8130_provenance.
- NP43808.RAmEQSqFSxhz0U0vUm-o0I-0zML3_9DmhIxhW_Kj3lOj4130_assertion description "[Our finding indicates that the prevalence of factor V Leiden, prothrombin G20210A and MTHFR C677T in G6PD deficient individuals is not statistically different compared to normal subjects and G6PD deficiency is not associated with these thrombophilic mutations in Western Iran.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43808.RAmEQSqFSxhz0U0vUm-o0I-0zML3_9DmhIxhW_Kj3lOj4130_provenance.
- NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_assertion description "[By means of mis-matched primers amplified the G6PD gene, the products were 234 bp, 280 bp and 345 bp in length, then restriction enzyme analysis was used to detect the most common Chinese G6PD mutations, 1376 G-->T, 1388 G-->A and 95 A-->G. The results showed that out of the 1,090 samples, 98 G6PD deficiency samples were found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43810.RAly8ECnXbA9F-COIKgh48Wm--vxB7oae9d7Ngtwi-chY130_provenance.
- NP43813.RAiBB_h6ugQnPSAk4Po-PdOhdn9oSrGynKHeGXOaPoIGQ130_assertion description "[Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common hereditary enzymopathy among Southeast Asians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43813.RAiBB_h6ugQnPSAk4Po-PdOhdn9oSrGynKHeGXOaPoIGQ130_provenance.
- NP43821.RAqwk-WzoHNfyOBtVU2_s5RTECpACjIwQNriG2HTDjy9k130_assertion description "[We found that G6PD A- heterozygous females (18 of 74) have a low prevalence of asymptomatic malaria (38.9% versus 67.3%; P = 0.03, by chi-square test).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43821.RAqwk-WzoHNfyOBtVU2_s5RTECpACjIwQNriG2HTDjy9k130_provenance.
- NP43824.RAjAwfV-34nbxLpaClGRcL9tIBtBABKtYLSzD6KCxhjTU130_assertion description "[The finding that haptoglobin 2-2 genotype is a risk factor for anaemia in children in a malaria-endemic area may reflect the reduced ability of the Hp2-2 polymer to scavenge free haemoglobin-iron following malaria-induced haemolysis. The magnitude of the effect of haptoglobin genotype (4 g/l Hb difference, p = 0.0009) was comparable to that of G6PD deficiency or HbAS (3 g/l difference, p = 0.03; and 2 g/l difference, p = 0.68, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43824.RAjAwfV-34nbxLpaClGRcL9tIBtBABKtYLSzD6KCxhjTU130_provenance.
- NP43826.RAlUy-4uWPeB3P5qdjKbyv2pRU9FkQV0NxyFSGKYxH1Wc130_assertion description "[Association of red cell glucose-6-phosphate dehydrogenase with haemoglobinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43826.RAlUy-4uWPeB3P5qdjKbyv2pRU9FkQV0NxyFSGKYxH1Wc130_provenance.
- NP43831.RAh7YKYEWMgCoWM5Y25H87lXOMYp00JjiBTA8EnqTLjg4130_assertion description "[, our results provide preliminary evidence that the variant allele of c.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43831.RAh7YKYEWMgCoWM5Y25H87lXOMYp00JjiBTA8EnqTLjg4130_provenance.
- NP43842.RAsjfCVFOnq2SHTIt7TbYZCRRht_wlvwUvg7snjMndRwM130_assertion description "[These findings highlight the importance of establishing the incidence and nature of molecular events that impact on Duffy expression in different populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43842.RAsjfCVFOnq2SHTIt7TbYZCRRht_wlvwUvg7snjMndRwM130_provenance.
- NP43844.RAiOn5KsefVCGHF0TuVKP1NUEu6FXglBHPc_b6s6HsZ6I130_assertion description "[High frequency of Friedreich's ataxia carriers in the Paphos district of Cyprus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43844.RAiOn5KsefVCGHF0TuVKP1NUEu6FXglBHPc_b6s6HsZ6I130_provenance.
- NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_assertion description "[ The lack of a statistically significant association between Lewis 'genotype' and subclinical atherosclerosis in our data suggests that earlier studies reporting associations at the 'phenotypic' level may reflect aspects of the biology of the Lewis system other than an inherent genetic property.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_provenance.
- NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_assertion description "[The frequency of the Le(a-b-) phenotype may vary substantially in different populations. Identification of this new genetic marker of obesity may, for example, contribute to the explanation of individual and ethnic differences in the prevalence of obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_provenance.
- NP43854.RAnrcbkIQQhPn-4d1OKzAZ5P_mDkLLjSKpS9gDzVzLbq0130_assertion description "[The null alleles of the FUT2 gene are another example of rare alleles occurring with unexpectedly high frequencies in distinct geographic regions or populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43854.RAnrcbkIQQhPn-4d1OKzAZ5P_mDkLLjSKpS9gDzVzLbq0130_provenance.
- NP43860.RArh_HA7-Ruo9xEOT4Qo2RXAyBpafTVnarccct8GnPLfE130_assertion description "[The ferritin L-chain is one of these genes, but the rare insertional mutations that cause neuroferritinopathy with basal ganglia degeneration have not yet been identified in PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43860.RArh_HA7-Ruo9xEOT4Qo2RXAyBpafTVnarccct8GnPLfE130_provenance.
- NP43882.RAvq8wFX5ip4o4zZRXkY4S1SnSczwuMEYXrvVtyywpt8o130_assertion description "[The AccI polymorphism in FSHbeta gene may be associated with PCOS in some women, especially those with obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43882.RAvq8wFX5ip4o4zZRXkY4S1SnSczwuMEYXrvVtyywpt8o130_provenance.
- NP43885.RAm43iF7SEvtDGMsGSn1P3PAl98UBDGFXfGTsLJdjw26A130_assertion description "[Radiographic osteoarthritis at three joint sites and FRZB, LRP5, and LRP6 polymorphisms in two population-based cohorts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43885.RAm43iF7SEvtDGMsGSn1P3PAl98UBDGFXfGTsLJdjw26A130_provenance.
- NP43886.RApI2XxvOvnO66XpSDtLGVl08f0SpKrtWkWi7rTIGi4Vw130_assertion description "[ The Pro 23 His and Pro 347 Leu mutations in the rhodopsin gene are representative mutations for ADRP in other countries, but the mutation in the rhodopsin gene is very rare in Japanese patients with ADRP. On the other hand, a novel 208 delG mutation in the FSCN 2 gene was identified in 14 patients from 4 Japanese families with ADRP. This mutation was found in 3.3% of patients with ADRP, which suggests that this mutation might be relatively common and characteristic in Japanese patients with ADRP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43886.RApI2XxvOvnO66XpSDtLGVl08f0SpKrtWkWi7rTIGi4Vw130_provenance.
- NP43891.RAh0-_gV7jnpAqz3OORjd_WwHflePGqIvqkuBUhSyR5OU130_assertion description "[FOXP2 might be involved in the language disorder in patients with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43891.RAh0-_gV7jnpAqz3OORjd_WwHflePGqIvqkuBUhSyR5OU130_provenance.
- NP43894.RApTWhQ08PrigJHW7HD5Rrylbr3xfBqSdyUHiSGq7AbC8130_assertion description "[Polymorphism of the polyalanine tract of thyroid transcription factor-2 gene in patients with thyroid dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43894.RApTWhQ08PrigJHW7HD5Rrylbr3xfBqSdyUHiSGq7AbC8130_provenance.
- NP43896.RAlVfPpWYCACaKRhsuXWdpSHUSLva_y-ul9aoxwuATUOI130_assertion description "[Identification of missense mutations in the hepatocyte nuclear factor-3beta gene in Japanese subjects with late-onset Type II diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43896.RAlVfPpWYCACaKRhsuXWdpSHUSLva_y-ul9aoxwuATUOI130_provenance.
- NP43900.RAoeQmsuwmVAaMt2T7DEJZJJF1EOctHuTS6pMnSfs8bEo130_assertion description "[ The promoter region of FR-alpha may harbor much more genetic variation than its highly conserved exons, and not just isolated, unique mutations. This could be a new factor contributing to gene-food interaction explaining part of the hyperhomocysteinemia panorama. Extended searches for polymorphisms further upstream in the FR-alpha gene are warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43900.RAoeQmsuwmVAaMt2T7DEJZJJF1EOctHuTS6pMnSfs8bEo130_provenance.
- NP43903.RAiLx029qUqMWJAFxTCzvO0oe3Ar4wOy4r6Y28-aVVyE0130_assertion description "[FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43903.RAiLx029qUqMWJAFxTCzvO0oe3Ar4wOy4r6Y28-aVVyE0130_provenance.
- NP43904.RAqh0l8h652_nJTj2tKmV05FZvVqiqaV7AGl2LlcsFglk130_assertion description "[ Over 30 triple CGG repeats denote increased risk (and severity) toward premature ovarian senescence in parallel to increasing expansions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43904.RAqh0l8h652_nJTj2tKmV05FZvVqiqaV7AGl2LlcsFglk130_provenance.
- NP43905.RAv4E0kEK1AIyTesM2w-uM0W-aT2PyhXOvVu4-xRKKPnI130_assertion description "[To study three molecular parameters (number of CGG repeats, X-inactivation ratio, and expression of FMR1 mRNA) in premutation carriers of fragile X syndrome with and without premature ovarian failure (POF) to find differences between these two groups that could be useful in reproductive counseling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43905.RAv4E0kEK1AIyTesM2w-uM0W-aT2PyhXOvVu4-xRKKPnI130_provenance.
- NP43908.RAv9qwAcHmNkAfWUrNsdMK9T4LZ1kmUQdiEoj1gppy-R0130_assertion description "[The influence of FMR1, INHalpha1, NAT2, GSTT1 and GSTM1 genes on ovarian function, and their association with POF and `poor response` to exogenous GT after ovulation stimulation were investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43908.RAv9qwAcHmNkAfWUrNsdMK9T4LZ1kmUQdiEoj1gppy-R0130_provenance.
- NP43909.RAo_rYQM7x1Cp8KW04zRPre8jRTxcqozZkHn2zwWGiUFI130_assertion description "[Fragile X syndrome, which is caused by expanded CGG repeats of the FMR1 gene, is associated with a broad spectrum of clinical involvement and is the most common inherited form of intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43909.RAo_rYQM7x1Cp8KW04zRPre8jRTxcqozZkHn2zwWGiUFI130_provenance.
- NP43912.RAugeTSCG6TvhTy-6xwm_66f_OigtDwUaFTiXw63bx_ss130_assertion description "[We report on the allele distribution in a normal Chilean population at 2 microsatellite loci neighbouring the FRAXA locus and at the CGG repeat in the 5' end of the FMR-1 gene, which causes the fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43912.RAugeTSCG6TvhTy-6xwm_66f_OigtDwUaFTiXw63bx_ss130_provenance.
- NP43914.RAm6YChEHXITsH16WHDi4_eIZ5wU5NMKD9CutYPyduTMg130_assertion description "[Regional grey and white matter density is significantly affected in male pre-mutation carriers of FraX recruited on the basis of genetic, not clinical, phenotype. The association of voxel density reduction and ageing is consistent with observations of a subgroup of older pre-mutation males who present with cognitive decline. Moreover, our findings suggest, for the first time, an association between voxel density reduction and genetic variation in FraX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43914.RAm6YChEHXITsH16WHDi4_eIZ5wU5NMKD9CutYPyduTMg130_provenance.
- NP43925.RAtkRV56l2HhroW9Vq_613cq2bofwNlsL3jZksELJHdcs130_assertion description "[Frequency of FMR1 premutation in individuals with ataxia and/or tremor and/or parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43925.RAtkRV56l2HhroW9Vq_613cq2bofwNlsL3jZksELJHdcs130_provenance.
- NP43928.RAmxSUp3ZviD_i5FMWMoeKmyKd2ofugHVZuql5-tPCq3o130_assertion description "[Association of FMR1 repeat size with ovarian dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43928.RAmxSUp3ZviD_i5FMWMoeKmyKd2ofugHVZuql5-tPCq3o130_provenance.
- NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_assertion description "[tatistically significant heterogeneity in the relative frequencies of single and multiple site alleles, haplotypes, and genotypes of the human FMO3 among ethnic subdivisions suggests that population differences in the susceptibility of humans to abnormal metabolism or adverse drug reactions for chemicals metabolized by human FMO3 could exist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43935.RAq8C2UCo1wOe-Ko7dhGi7yGf9y43Lesr5qWRAUqXcOl8130_provenance.
- NP43936.RAlms861Awgb9Z2RNGNTvJqvcZjchI9qfZzaHg4wxqKtA130_assertion description "[Based on the functional activity of the variant FMO3 enzymes, it is likely that population differences exist for compounds primarily metabolized by FMO3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43936.RAlms861Awgb9Z2RNGNTvJqvcZjchI9qfZzaHg4wxqKtA130_provenance.
- NP43941.RApEtjl-P8bSrVQqmxDEZd_uAIxI47C5NuW7KybmHXcG4130_assertion description "[Genetic polymorphisms of flavin monooxygenase 3 in sulindac-induced regression of colorectal adenomas in familial adenomatous polyposis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43941.RApEtjl-P8bSrVQqmxDEZd_uAIxI47C5NuW7KybmHXcG4130_provenance.
- NP43946.RAmz2G7jH9MHJ5hW5YcGrr6Dfbs2zoFFx_yFWAJ_83XoA130_assertion description "[High-FLT3 expression may be a poor prognostic factor for AML patients without FLT3/ITD mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43946.RAmz2G7jH9MHJ5hW5YcGrr6Dfbs2zoFFx_yFWAJ_83XoA130_provenance.
- NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_assertion description "[We studied a series of 68 subjects diagnosed with childhood acute myeloid leukemia (AML) using conventional cytogenetics and fluorescence in situ hybridization (FISH), polymerase chain reaction (PCR) to analyze mutations in FLT3 and NPM1 genes, and/or array comparative genomic hybridization (CGH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43951.RAu9BlNkxAxSPkvthj3d8EVp6HZAV9SbzRcquC_M8fIkY130_provenance.
- NP43953.RAm4HJUOHAlNLtZE1Tlsu7sjQn4VPxSiEyyg9DCzvvi-A130_assertion description "[A study of NPM1 and FLT3 gene mutations in acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43953.RAm4HJUOHAlNLtZE1Tlsu7sjQn4VPxSiEyyg9DCzvvi-A130_provenance.
- NP43954.RAtMa7ZnNmEkhfHuRXqr33UHVSTbGHMxWhE6Qyt1r-Qoo130_assertion description "[In conclusion, this study demonstrates that NPM1+/FLT3-LM- mutations are an independent predictor for a favorable outcome in AML with normal karyotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43954.RAtMa7ZnNmEkhfHuRXqr33UHVSTbGHMxWhE6Qyt1r-Qoo130_provenance.
- NP43958.RAknZbDi6o4AFiwmkI1bcpmzd8m--Cj_x0tPfaZLfnMko130_assertion description "[The prognostic significance of IDH1 mutations in younger adult patients with acute myeloid leukemia is dependent on FLT3/ITD status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43958.RAknZbDi6o4AFiwmkI1bcpmzd8m--Cj_x0tPfaZLfnMko130_provenance.
- NP43960.RAh8HVOXuIXIwF5ODlO3kTHzvsfV1TO8plLx8NTr2vp_0130_assertion description "[Cuplike nuclei in AML were highly associated with the presence of NPM1 and FLT3-ITD mutations and with several clinicopathologic and immunophenotypic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43960.RAh8HVOXuIXIwF5ODlO3kTHzvsfV1TO8plLx8NTr2vp_0130_provenance.
- NP43962.RAozC7QmAuKXV_s1nLji928BcGfD0dkkO4o2pV7VJar_o130_assertion description "[Data from mutation analyses of the NPM1, CEBPA, FLT3, and MLL genes were correlated with outcome in patients 61 years and older treated within the AML HD98B trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43962.RAozC7QmAuKXV_s1nLji928BcGfD0dkkO4o2pV7VJar_o130_provenance.
- NP43964.RAvkHZHMpRXM7ppjxNquYEZDgZyu5wXFI-XpdCvE3Avow130_assertion description "[Mutations in the fms-like tyrosine kinase 3 (FLT3) gene containing an internal tandem duplication (FLT3/ITD) or mutations in the nucleophosmin 1 gene (NPM1) are thought to be prognostic indicators in acute myeloid leukemia (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43964.RAvkHZHMpRXM7ppjxNquYEZDgZyu5wXFI-XpdCvE3Avow130_provenance.
- NP43973.RAksZveJj1cyjJ1bCJ05ydtzZEj2fhOmMwQNOhHmUZ4jE130_assertion description "[FLT3 mutations (FLT3-ITD or FLT3-TKD) are frequently identified in patients with newly diagnosed APL, both mutations are associated with higher initial WBC and short type PML-RAR alpha isoforms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43973.RAksZveJj1cyjJ1bCJ05ydtzZEj2fhOmMwQNOhHmUZ4jE130_provenance.
- NP43980.RAspLkSzu2ybUCU2NXxm7YXXj5nuGdXJS6sjSNayiK-oU130_assertion description "[Association of EWS-FLI1 type 1 fusion with lower proliferative rate in Ewing's sarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43980.RAspLkSzu2ybUCU2NXxm7YXXj5nuGdXJS6sjSNayiK-oU130_provenance.
- NP43981.RAiOyEm1_x-OxHtvYKWQrHLthG9vtZb5FHbOhyWjSK6gA130_assertion description "[Thus, we investigated the influence of transporters associated with antigen processing (TAP), human leukocyte antigen (HLA)-DQB1, and HLA-DRB1 gene polymorphism in mestizo Colombian patients with pSS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43981.RAiOyEm1_x-OxHtvYKWQrHLthG9vtZb5FHbOhyWjSK6gA130_provenance.
- NP43982.RAtQ_F80JxJOgf6aJ02W5zqenzD403WUcqS-k2RLbN6ds130_assertion description "[Our study thus suggests possible involvement of EDNRA in essential HT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43982.RAtQ_F80JxJOgf6aJ02W5zqenzD403WUcqS-k2RLbN6ds130_provenance.
- NP43985.RAsERdkjddepcLWnFU_YIfmb2nI71kTaoqMW_o6GXghho130_assertion description "[FKBP5 polymorphisms and antidepressant response in geriatric depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43985.RAsERdkjddepcLWnFU_YIfmb2nI71kTaoqMW_o6GXghho130_provenance.
- NP43991.RAq5B8xmZvBZaPM0XXRnMkBV1aLr7ZDHsHxrRFJx4oafY130_assertion description "[The sorted genes allow us to draw novel hypotheses for future studies of HCV infection to ultimately identify bona fide genes and their variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43991.RAq5B8xmZvBZaPM0XXRnMkBV1aLr7ZDHsHxrRFJx4oafY130_provenance.
- NP43993.RAkbXKfjVMaqIWoIA7ub6q8yZJQMVZJPmGrPb-ykgIvMI130_assertion description "[Of the four haplotypes inferred using the FGA -58G>A and FGG 1299 +79T>C SNPs, the most frequent haplotype, FGG-FGA*1 (prevalence 46.6%), was associated with increased risk of MI (OR 1.51; 95%CI 1.18, 1.93), whereas the least frequent haplotype, FGG-FGA*4 (11.8%), was associated with lower risk of MI (OR 0.79 95%CI 0.64, 0.98).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43993.RAkbXKfjVMaqIWoIA7ub6q8yZJQMVZJPmGrPb-ykgIvMI130_provenance.