Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP43117.RArTWZeufrWjafGOLyW_gLj4o_kJaNmWoVBwYwpuEuLqE130_assertion description "[GSTM1 polymorphism along with PM10 exposure contributes to the risk of preterm delivery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43117.RArTWZeufrWjafGOLyW_gLj4o_kJaNmWoVBwYwpuEuLqE130_provenance.
- NP43118.RAhOu8BcDHBqFc3cQwg-_1JG64JW2utYQ2BQNiy2_ZFc4130_assertion description "[Oxidative stress-related gene interactions with preterm delivery in Korean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43118.RAhOu8BcDHBqFc3cQwg-_1JG64JW2utYQ2BQNiy2_ZFc4130_provenance.
- NP43119.RAhWYeoA08gYOCYhrtjjbWla8NfoC_ry-EHM0J3zXB_rI130_assertion description "[Polymorphic variations in GSTM1, GSTT1, PgP, CYP2D6, CYP3A5, and dopamine D2 and D3 receptors and their association with tardive dyskinesia in severe mental illness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43119.RAhWYeoA08gYOCYhrtjjbWla8NfoC_ry-EHM0J3zXB_rI130_provenance.
- NP43124.RAkvofxIiapbK1NfmUiGJh0KWY-f8arat_oDwTxuLWZNo130_assertion description "[The impact of the GSTM1 null genotype on oral cancer risk was also analyzed in separate groups of individuals with different tobacco habits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43124.RAkvofxIiapbK1NfmUiGJh0KWY-f8arat_oDwTxuLWZNo130_provenance.
- NP43125.RAhhJqcN9N2PCYPn1LAIw34ihVnGTimatkRwKsTzcIJos130_assertion description "[ Nuclear genetic polymorphisms related to oxidative stress or apoptosis may modify the age at onset of LHON.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43125.RAhhJqcN9N2PCYPn1LAIw34ihVnGTimatkRwKsTzcIJos130_provenance.
- NP43128.RArGYj6ra0x0LmCtKJwhxveXYjjc7iHij_msBdDu_dwDE130_assertion description "[We found that the GSTM1-null allele was more prevalent in active smoking endometriosis patients (63.4%) than in the controls (35.0%), and the difference was statistically significant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43128.RArGYj6ra0x0LmCtKJwhxveXYjjc7iHij_msBdDu_dwDE130_provenance.
- NP43129.RAnlSj1Py3gPv1enK4to9-txwnMtAxZo4O5rsWLGgij_E130_assertion description "[In conclusion, our findings suggest that the GSTM1, GSTT1 and GSTP1 genetic polymorphisms are not associated with the development of endometriosis in Korean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43129.RAnlSj1Py3gPv1enK4to9-txwnMtAxZo4O5rsWLGgij_E130_provenance.
- NP43132.RAiIT6xVtojCqj6Hw7eXgtXQAgSU3yZeDz5-cBf15RESE130_assertion description "[Polymerase chain reaction was used to identify the GSTM1 genotypes in 76 patients with endometriosis and 80 controls (surgical patients for gynecological problems other than endometriosis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43132.RAiIT6xVtojCqj6Hw7eXgtXQAgSU3yZeDz5-cBf15RESE130_provenance.
- NP43138.RAlf2QG4nEb9PI2U2JGI1nnAqNp8wMspcRTrtQNsGJXKQ130_assertion description "[GSTM1 (0/0) gene polymorphism may be linked to prostate cancer risk and early age of onset in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43138.RAlf2QG4nEb9PI2U2JGI1nnAqNp8wMspcRTrtQNsGJXKQ130_provenance.
- NP43145.RAmxf-ettTjg4KGfvQ5_vaSFDoWgfVLsBVm9Umq1hkflc130_assertion description "[To assess whether CYP1A1, GSTM1, GSTT1 susceptibility genotypes, smoking status and alcohol consumption factors contribute to PCa risk, gene-gene and gene-environment interactions were analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43145.RAmxf-ettTjg4KGfvQ5_vaSFDoWgfVLsBVm9Umq1hkflc130_provenance.
- NP43156.RAjg9WUFXa-0KC2dK3w1Z4bLbd4TOTw82AGiUFGh4VsJ4130_assertion description "[In the current study, risk factors for developing cervical cancer were tobacco smoking and GSTM1 null; however, no association was observed between these two factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43156.RAjg9WUFXa-0KC2dK3w1Z4bLbd4TOTw82AGiUFGh4VsJ4130_provenance.
- NP43158.RApHzEUUvHniIg9pIfASXvXdGKK5dHJR7L8Z1mHuGpnDM130_assertion description "[Chronic obstructive pulmonary disease. 1: Susceptibility factors for COPD the genotype-environment interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43158.RApHzEUUvHniIg9pIfASXvXdGKK5dHJR7L8Z1mHuGpnDM130_provenance.
- NP43160.RAvB_dydX6sn_nEozpCziqe6C-NG8J0f9fM-ZyHCbehSU130_assertion description "[The GSTM1 gene is a genetic contributor to overall COPD susceptibility in non-Asian populations, and the GSTT1 gene is not associated with COPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43160.RAvB_dydX6sn_nEozpCziqe6C-NG8J0f9fM-ZyHCbehSU130_provenance.
- NP43167.RAkZSykx6nsgz5bPRmMFFFjanO5F_uGy5gIoluiN9-UZg130_assertion description "[Polymorphisms of GSTT1, GSTM1 and GSTP1 genes are unlikely to be involved in the pathogenesis of COPD in Chinese in Hong Kong and Southern China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43167.RAkZSykx6nsgz5bPRmMFFFjanO5F_uGy5gIoluiN9-UZg130_provenance.
- NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_assertion description "[To evaluate the occurrence of homozygous deletions of the GSTM1 and GSTT1 genes in women with sporadic breast cancer and in women without cancer and to compare breast cancer mammographic features between patients with and without these deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_provenance.
- NP43175.RApDlUoO-wBT0srIGGiZgQD4DSIeL95_wZz4JrXfyHbFA130_assertion description "[The aim of this study was to investigate associations between genetic variability in specific Glutathione S-transferases (GST) genes (GSTM1, GSTT1 and GSTP1) and susceptibility to breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43175.RApDlUoO-wBT0srIGGiZgQD4DSIeL95_wZz4JrXfyHbFA130_provenance.
- NP43177.RAqfJ6NLDnm6i6j4YhbKaMi-aIcfYR2IM7q-u9eUx841U130_assertion description "[The results conclusively show that single gene GSTM1 polymorphisms do not confer a substantial risk of breast cancer to its carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43177.RAqfJ6NLDnm6i6j4YhbKaMi-aIcfYR2IM7q-u9eUx841U130_provenance.
- NP43179.RAqwucBCrNKRux0CmAhzzbpVxFo_zldk31KvzIVr1L4HQ130_assertion description "[Our results suggest that the XRCC1 399Gln allele is a potentially important determinant of susceptibility to smoking-induced pancreatic cancer. Our findings, including stronger associations and interactions among women, require replication in additional study populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43179.RAqwucBCrNKRux0CmAhzzbpVxFo_zldk31KvzIVr1L4HQ130_provenance.
- NP43183.RAm45tYFzt97rE5zvRX1U6YCpb-ZBm4TC7fhFQFAZ3KfE130_assertion description "[ The results suggest that genetic polymorphism of GSTM1 was susceptible to HCC and individuals who are GSTM1-null have an increased risk of developing HCC. There is evidence of interaction between GSTM1 polymorphism and AFB1 exposure, especially with low/median degrees of AFB1 exposure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43183.RAm45tYFzt97rE5zvRX1U6YCpb-ZBm4TC7fhFQFAZ3KfE130_provenance.
- NP43184.RAkk62P3oc-BLojEfghSXiwOW-7wPjll-P-kTdj0eq3Vo130_assertion description "[our data suggested that CYP1B1 germ line-inactivating mutations might increase the incidence of HCA in women with HNF1alpha mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43184.RAkk62P3oc-BLojEfghSXiwOW-7wPjll-P-kTdj0eq3Vo130_provenance.
- NP43197.RApxrTQIYsz25o0W1WcaXctbTMiA3MV67kqq_GAd-Dk4U130_assertion description "[Interaction of the glutathione S-transferase genes and cigarette smoking on risk of lower extremity arterial disease: the Atherosclerosis Risk in Communities (ARIC) study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43197.RApxrTQIYsz25o0W1WcaXctbTMiA3MV67kqq_GAd-Dk4U130_provenance.
- NP43199.RAoBDEBofv8Y4Yclh_oYOIQWLhUfdR68Yw7AEZBvXM0Fw130_assertion description "[Glutathione S-transferase M1, T1, and P1 gene polymorphisms and carotid atherosclerosis in Korean patients with rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43199.RAoBDEBofv8Y4Yclh_oYOIQWLhUfdR68Yw7AEZBvXM0Fw130_provenance.
- NP43206.RAlHj-CePugyks98XdXWlBpUhQf_qHViQV7jYC93-69ms130_assertion description "[GSTM1 null genotype was significantly associated with the increased risk of asthma (P = .002).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43206.RAlHj-CePugyks98XdXWlBpUhQf_qHViQV7jYC93-69ms130_provenance.
- NP43210.RAurbwgc6GLV_72sN3h-AwBs0Tfdy-mrL2a-ggdSKYYmc130_assertion description "[Genetic polymorphisms in the glutathione S-transferase P1 gene (GSTP1) and the glutathione S-transferase M1 gene (GSTM1) have been implicated as risk factors for asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43210.RAurbwgc6GLV_72sN3h-AwBs0Tfdy-mrL2a-ggdSKYYmc130_provenance.
- NP43217.RArySBZXrkkfp7SX042kI80ND8OOdNj6MUApljv7gZOuE130_assertion description "[GSTM1 and codon 72 P53 polymorphism in multiple myeloma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43217.RArySBZXrkkfp7SX042kI80ND8OOdNj6MUApljv7gZOuE130_provenance.
- NP43219.RAhXM-zUukDRQdxbJm3cSJNf3rhVWpoGGT-1LUQlBysuk130_assertion description "[Susceptibility to urinary bladder cancer: relevance of rs9642880T, GSTM1 0/0 and occupational exposure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43219.RAhXM-zUukDRQdxbJm3cSJNf3rhVWpoGGT-1LUQlBysuk130_provenance.
- NP43222.RAqw9wksz3o4msW4a0k-ToFPi_U6L_V2nnotgM6L7lWCc130_assertion description "[The aim of the study was to investigate NAT1, NAT2, GSTM1, GSTT1, GSTP1, SULT1A1, XRCC1, XRCC3 and XPD genetic polymorphisms, coffee consumption and risk of bladder cancer (BC) through a hospital-based case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43222.RAqw9wksz3o4msW4a0k-ToFPi_U6L_V2nnotgM6L7lWCc130_provenance.
- NP43228.RAg5R88898H3yIY4waZxt5VxUiV2LTZikk7bWAddMGc60130_assertion description "[To determine whether polymorphisms of tumor necrosis factor-alpha (TNF-alpha), vascular endothelial growth factor (VEGF), human 8-oxoguanine DNA glycosylase 1 (hOGG1), glutathione S-transferase-mu (GSTM1), and glutathione S-transferase-phi (GSTT1) are risk factors for bladder cancer among Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43228.RAg5R88898H3yIY4waZxt5VxUiV2LTZikk7bWAddMGc60130_provenance.
- NP43234.RAphiLhkV-1NdX4lu8xfzMdG7kmRkN3hFTz26F-O5jdfM130_assertion description "[We prospectively collected peripheral blood lymphocytes from 313 patients with Hodgkin lymphomas to analyze GSTP1, GSTM1, GSTT1, UGT1A1, and CYP3A4 enzyme gene polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43234.RAphiLhkV-1NdX4lu8xfzMdG7kmRkN3hFTz26F-O5jdfM130_provenance.
- NP43237.RAoTXtqe4imbiSKkrXMjzy8jsyY1y_rmIE_WVMaIk_M7k130_assertion description "[Polymorphisms interact to influence antileukemic outcome, and represent determinants of response that can be used to optimize therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43237.RAoTXtqe4imbiSKkrXMjzy8jsyY1y_rmIE_WVMaIk_M7k130_provenance.
- NP43238.RAle7kjVaMeiugu0D3XUnBDxcmeIgjQaavLGh3Nf9ALs4130_assertion description "[Genetic polymorphism of glutathione-S-transferase M1 and T1 in children with acute lymphoblastic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43238.RAle7kjVaMeiugu0D3XUnBDxcmeIgjQaavLGh3Nf9ALs4130_provenance.
- NP43241.RAgC6NxnWxeQKQDKJMEEepCry4grrdMAIS8im91goKQuk130_assertion description "[ Logistic regression model can be used to evaluate gene-environment interaction and dose-response of exposure-gene effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43241.RAgC6NxnWxeQKQDKJMEEepCry4grrdMAIS8im91goKQuk130_provenance.
- NP43251.RAgukFgCvTS2C3lUWEyxAwntKrNQupL75by3g6Os2YRfU130_assertion description "[ In high-risk area, nasopharyngeal carcinoma patients and local residents have high frequency of GSTM1 and/or GSTT1 gene deletion. It suggests that a genetic susceptibility to putative chemical carcinogens may be responsible for NPC clustering in the high-risk area studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43251.RAgukFgCvTS2C3lUWEyxAwntKrNQupL75by3g6Os2YRfU130_provenance.
- NP43252.RArxAFhCs21K7vyHP255Vx1PNiRja7Y4wUEqVMly7QTZU130_assertion description "[the increase of nasopharyngeal carcinoma risk in Tunisia seems to be associated with GSTM10/0 and NAT2*6/6 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43252.RArxAFhCs21K7vyHP255Vx1PNiRja7Y4wUEqVMly7QTZU130_provenance.
- NP43262.RAiziu1IV7b8D_DLzMHvGGrDmC5LbVkzguzwc1zAc7k_g130_assertion description "[Four-hundred PD cases (age at onset: 60.0 +/- 10.7 years) were genotyped for common polymorphisms in GSTM1, P1, T1 and Z1 using well-established methods.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43262.RAiziu1IV7b8D_DLzMHvGGrDmC5LbVkzguzwc1zAc7k_g130_provenance.
- NP43271.RAiqWPl539OHe3oVsbfnT4CqvKLmpwraP3rqYV_qGPyss130_assertion description "[Glutathione-S-transferase-1 and interleukin-1beta gene polymorphisms in Japanese patients with Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43271.RAiqWPl539OHe3oVsbfnT4CqvKLmpwraP3rqYV_qGPyss130_provenance.
- NP43275.RAgP8gHRUwbWYH3HvF2b6Qx_T4RBNxyyiKlzziy9Fqdj0130_assertion description "[GSTM1 polymorphisms seem to be involved in BCC risk, while GSTM1 null/null genotype combined with CYP1A1 allele Val(462) are associated with a higher risk for SCC, indicating that allelism and/or interactions between allelic variants at other loci may also influence the risk of NMSC, particularly SCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43275.RAgP8gHRUwbWYH3HvF2b6Qx_T4RBNxyyiKlzziy9Fqdj0130_provenance.
- NP43276.RAgbIPVzJ9DU_4uf4yfvHC6ut_soUg-HVsO_4ahAJdIEA130_assertion description "[Patients with Basal Cell Skin Carcinoma (BCC) presented the combined GSTM1-GSTT1+ genotype more frequently (49.1%) than controls (29.8%) (Fisher test; p=0.04), conferring a 2.273 (Odds Ratio; 95% CI=1.199-4.308) higher risk for BCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43276.RAgbIPVzJ9DU_4uf4yfvHC6ut_soUg-HVsO_4ahAJdIEA130_provenance.
- NP43279.RAoDnoKcGWXoH80nOPlDhWVmJY3c8JhJqmpF6ywTVt_Hc130_assertion description "[There was no independent association between SLE and presence of the homozygous null GSTM1 or GSTT1 genotype, the homozygous Val/Val or heterozygous Val/Ile GSTP1 genotype, or occupational sunlight exposure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43279.RAoDnoKcGWXoH80nOPlDhWVmJY3c8JhJqmpF6ywTVt_Hc130_provenance.
- NP43281.RAgjEG1eZvE4Rup1JZyklMoeWM8hTB-7aurQrSfoObT_M130_assertion description "[There seems to be an increased risk for AA and MDS in individuals lacking GSTT1 or both GSTM1/GSTT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43281.RAgjEG1eZvE4Rup1JZyklMoeWM8hTB-7aurQrSfoObT_M130_provenance.
- NP43285.RAh8BHBSlSGzcZb3EY0KupiXCMhROU_z19mH6aa0JZyEM130_assertion description "[Our previous study of a Chinese population found the GSTM1 null genotype to be associated with an increased risk of lung AC, and the combination of GSTM1 null genotype and CYP2E1 wild type conferred a significantly elevated risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43285.RAh8BHBSlSGzcZb3EY0KupiXCMhROU_z19mH6aa0JZyEM130_provenance.
- NP43288.RAv_Ot_iG_vqAmABU2YdVYxV9IkfRLv4MGfRqWXDew4Tc130_assertion description "[ Our data suggest that disease outcome in female RA patients with a history of smoking is significantly worse than in those who have never smoked. Smoking was associated with the most severe disease in patients who carried the GSTM1-null polymorphism. This association may be due in part to a relationship between the GSTM1 polymorphism and RF production in smokers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43288.RAv_Ot_iG_vqAmABU2YdVYxV9IkfRLv4MGfRqWXDew4Tc130_provenance.
- NP43290.RAtpvmxEKT0ktH9wLzZtL7PowAWoJuIAMJTZSz-KQpqDM130_assertion description "[Our findings suggest that the GSTM1*0 is associated with an increased susceptibility to schizophrenia, particularly disorganized type of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43290.RAtpvmxEKT0ktH9wLzZtL7PowAWoJuIAMJTZSz-KQpqDM130_provenance.
- NP43293.RAmaDWdpTLk8XXMkadcM0iyB2Pc2aV1oNDitEealgVuI0130_assertion description "[Glutathione S-transferase M1 polymorphism may contribute to schizophrenia in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43293.RAmaDWdpTLk8XXMkadcM0iyB2Pc2aV1oNDitEealgVuI0130_provenance.
- NP43304.RAiaJDtL5_Z4-Ft4nzWnAwCgMP7UPelfKIc0TNiIXqaEY130_assertion description "[The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43304.RAiaJDtL5_Z4-Ft4nzWnAwCgMP7UPelfKIc0TNiIXqaEY130_provenance.
- NP43313.RAtnQhzftSAe7hXXiEszvMrjzKGbiqOF-grUbNZpx1zgA130_assertion description "[Effects of glutathione S-transferase A1 (GSTA1) genotype and potential modifiers on breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43313.RAtnQhzftSAe7hXXiEszvMrjzKGbiqOF-grUbNZpx1zgA130_provenance.
- NP43314.RAkGbp9NL-_ARmapCyiTniRfwu7CJ3oNXra8e5zeY4ogM130_assertion description "[Polymorphisms of glutathione S-transferase A1 and O1 and breast cancer among postmenopausal Danish women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43314.RAkGbp9NL-_ARmapCyiTniRfwu7CJ3oNXra8e5zeY4ogM130_provenance.
- NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_assertion description "[Results warrant interest for the variants of genes pertaining to the molecular clock as possible endophenotypes of bipolar disorder, but caution ought to be taken in interpreting these preliminary results and future replication studies must be awaited.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_provenance.
- NP43325.RAiTVEU4z3MfS9-1irnUxoEwKwpkxCzLb3aDE8gF9Rv9w130_assertion description "[Increase in GSK3beta gene copy number variation in bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43325.RAiTVEU4z3MfS9-1irnUxoEwKwpkxCzLb3aDE8gF9Rv9w130_provenance.
- NP43327.RAi9Hr0IvNcvMPpvr2Ivin01e5OunJKt31H4lyX2hglS0130_assertion description "[These data suggest that the SNPs in DRD2 and AKT1 may influence the treatment response to risperidone in schizophrenia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43327.RAi9Hr0IvNcvMPpvr2Ivin01e5OunJKt31H4lyX2hglS0130_provenance.
- NP43331.RAl6sFhINKGkB9FZDnB3DvWrwkzPMGV4LfjBCncBWGpvs130_assertion description "[A case-control association study identified a significant difference in allele frequency distribution between schizophrenics and controls (P = 0.04). This is suggestive of involvement of the GRM5 gene in schizophrenia in this population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43331.RAl6sFhINKGkB9FZDnB3DvWrwkzPMGV4LfjBCncBWGpvs130_provenance.
- NP43336.RAnfSx6QwU-XNlvhx1GHIEnuCk1Zi0nHuY_KsGSPcDK8M130_assertion description "[A sample of 242 families with affected offspring and five single nucleotide markers located in the genomic region of GRM3 has been used to replicate association with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43336.RAnfSx6QwU-XNlvhx1GHIEnuCk1Zi0nHuY_KsGSPcDK8M130_provenance.
- NP43338.RAo9azWXqKBxAQTDUX8ycxGkm6cAPTydr2NvzR4mOgLUY130_assertion description "[We focused on the metabotropic glutamate receptor type 3 gene (GRM3) as a candidate for schizophrenia susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43338.RAo9azWXqKBxAQTDUX8ycxGkm6cAPTydr2NvzR4mOgLUY130_provenance.
- NP43340.RAtiAGAgRDJeEb0EFN1b3vQ4seXs9pyCZwn55KWABBc40130_assertion description "[Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43340.RAtiAGAgRDJeEb0EFN1b3vQ4seXs9pyCZwn55KWABBc40130_provenance.
- NP43343.RAie9MqolIvPajxQJXfIOwA8CoKgl4_SlBEeoepl2fPk8130_assertion description "[Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43343.RAie9MqolIvPajxQJXfIOwA8CoKgl4_SlBEeoepl2fPk8130_provenance.
- NP43347.RAtyPTr_rkMIyd47PPqBDIPM3D_6B1N7eSfCFTTOJYsaE130_assertion description "[Association study with 33 single-nucleotide polymorphisms in 11 candidate genes for hypertension in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43347.RAtyPTr_rkMIyd47PPqBDIPM3D_6B1N7eSfCFTTOJYsaE130_provenance.
- NP43349.RAqrhW3FPL6MCBctHaEg8FbvV8D-25dvKY5FMDpZg8rKA130_assertion description "[The purpose of this study was to determine if variants in the G-protein coupled receptor Kinase-4 (GRK4), nitric oxide synthase-3 (NOS3), or angiotensin converting enzyme (ACE) genes are associated singly or through complex interactions, with HBP in African Americans aged 18-49 years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43349.RAqrhW3FPL6MCBctHaEg8FbvV8D-25dvKY5FMDpZg8rKA130_provenance.
- NP43356.RAgtoVfvwf9XK9p0tTz5VJFkEzVq0E3VU32Ab-rNdhITM130_assertion description "[Genetic variations in NR2A have the greatest relevance for human alcohol dependence among the glutamatergic genes selected for their known alteration of alcohol effects in animal models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43356.RAgtoVfvwf9XK9p0tTz5VJFkEzVq0E3VU32Ab-rNdhITM130_provenance.
- NP43358.RAoDJE4_vCwonie5mcvUCdVtguEgTsLx-OaEs9WXlo8YY130_assertion description "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43358.RAoDJE4_vCwonie5mcvUCdVtguEgTsLx-OaEs9WXlo8YY130_provenance.
- NP43359.RAmbjLiJ_M-o-HSl-DhYgCvgnu7M8I7h0gajI162NXjcc130_assertion description "[An association study of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) and NR2B subunit gene (GRIN2B) in schizophrenia with universal DNA microarray.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43359.RAmbjLiJ_M-o-HSl-DhYgCvgnu7M8I7h0gajI162NXjcc130_provenance.
- NP43361.RAkcSLBTatH1erlXpn00jhxxfZJ6fVmTfkM15ZiBBYMj0130_assertion description "[Identification of a novel variant of the human NR2B gene promoter region and its possible association with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43361.RAkcSLBTatH1erlXpn00jhxxfZJ6fVmTfkM15ZiBBYMj0130_provenance.
- NP43362.RAtNZ5P2feSG_p0WbGnwWJ1izv7_oM3XEDY5uQ6m3TXo4130_assertion description "[Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43362.RAtNZ5P2feSG_p0WbGnwWJ1izv7_oM3XEDY5uQ6m3TXo4130_provenance.
- NP43372.RAqjrz_kBKI6_tx0uM1xNfgEppXUj5sfXpXwbQaHd96ms130_assertion description "[NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43372.RAqjrz_kBKI6_tx0uM1xNfgEppXUj5sfXpXwbQaHd96ms130_provenance.
- NP43375.RAvmRUZ8R93IFm32T5DVX5rzBz9c9ovl20TEUVYRsa52I130_assertion description "[Our results suggest that the NMDAR1 subunit is not frequently involved in the development of schizophrenia in the German population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43375.RAvmRUZ8R93IFm32T5DVX5rzBz9c9ovl20TEUVYRsa52I130_provenance.
- NP43378.RAi-0SAest3_OIun4a_21vY6mApJZQzmRTWriRyqP43B8130_assertion description "[N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) in schizophrenia: TDT and case-control analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43378.RAi-0SAest3_OIun4a_21vY6mApJZQzmRTWriRyqP43B8130_provenance.
- NP43379.RArSP41nPJlfUEtxqpOeADrcwaQoRVI5W2kh-gsmxZ9dg130_assertion description "[Association between the G1001C polymorphism in the GRIN1 gene promoter and schizophrenia in the Iranian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43379.RArSP41nPJlfUEtxqpOeADrcwaQoRVI5W2kh-gsmxZ9dg130_provenance.
- NP43381.RAi1fHgZDaS1VTFNwQ7jz5dUt6eIp6dR0PYAGgNVaUQeE130_assertion description "[ These results suggest that variants in NMDAR genes are associated with alcoholism and related traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43381.RAi1fHgZDaS1VTFNwQ7jz5dUt6eIp6dR0PYAGgNVaUQeE130_provenance.
- NP43393.RAsxmflYFjvb9uky-1sYq-JlT9cLxljSA4XM32ERqggP4130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43393.RAsxmflYFjvb9uky-1sYq-JlT9cLxljSA4XM32ERqggP4130_provenance.
- NP43401.RArtYGVBj2kQAfhCAqvs_wRjaEsPFzTGqb7N2pQhlew7c130_assertion description "[Glutamate receptor 6 gene (GluR6 or GRIK2) polymorphisms in the Indian population: a genetic association study on autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43401.RArtYGVBj2kQAfhCAqvs_wRjaEsPFzTGqb7N2pQhlew7c130_provenance.
- NP43407.RAhMerWheOZrVNGTYpoZb1v9n9DiVEH5qboFChR_pnPoM130_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." NP43407.RAhMerWheOZrVNGTYpoZb1v9n9DiVEH5qboFChR_pnPoM130_provenance.
- NP43414.RAuO4li-Y_Xn8IdIInRJrEFi-oxLLcaCgf01hyaHllNNY130_assertion description "[Due to its high prevalence, the hGPX1 variant may contribute significantly to lung cancer risk among Caucasians but not among ethnic Chinese who do not exhibit this polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43414.RAuO4li-Y_Xn8IdIInRJrEFi-oxLLcaCgf01hyaHllNNY130_provenance.
- NP43417.RAtfRrVZTmFKceJVRPxFvKSHBVuGffpMpRd5wjDadXF4Y130_assertion description "[Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43417.RAtfRrVZTmFKceJVRPxFvKSHBVuGffpMpRd5wjDadXF4Y130_provenance.
- NP43419.RAlKUnhzma11GQcmQFbqJsGEF8eYn7_b44I0KZXQqsrwc130_assertion description "[These results suggest that GSTM4 polymorphisms are biomarkers for the prediction of cisplatin response. ABCC4 polymorphisms, as well as GSTT1 copy number, may also help to predict cisplatin response, but further validation is required. These results represent a step toward the individualized chemotherapy of lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43419.RAlKUnhzma11GQcmQFbqJsGEF8eYn7_b44I0KZXQqsrwc130_provenance.
- NP43420.RAmoLBag0Sud_9yrxPJkBLOhpQMtOcqiBWVJjSXUrc_yY130_assertion description "[Smoking is the most important risk factor for young lung cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43420.RAmoLBag0Sud_9yrxPJkBLOhpQMtOcqiBWVJjSXUrc_yY130_provenance.
- NP43426.RAnedzHPegpv_4horAGxaxSaLDQoAF64IFEAK0Dtf9EVo130_assertion description "[GPX1 Pro198Leu polymorphism and breast cancer risk: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43426.RAnedzHPegpv_4horAGxaxSaLDQoAF64IFEAK0Dtf9EVo130_provenance.
- NP43431.RAlYP7tijmUFKrkgEPaQHp6zXRnq_NuKcZF-5lgpEPy8k130_assertion description "[Frequency of polymorphisms pro198leu in GPX-1 gene and ile58thr in MnSOD gene in the altitude Ecuadorian population with bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43431.RAlYP7tijmUFKrkgEPaQHp6zXRnq_NuKcZF-5lgpEPy8k130_provenance.
- NP43436.RAmthp8XBls84SAZWLLRzUaruTCHDLpJp96Tkhe47kGzA130_assertion description "[This study analysed 12 single-nucleotide polymorphisms (SNPs) in selenoprotein genes glutathione peroxidase 1 (GPX1), GPX4, 15 kDa selenoprotein (SEP15), selenoprotein S (SELS), selenoprotein P (SEPP1) and thioredoxin reductase 2 (TXNRD2) and in genes that code for a key protein in Se incorporation SECIS-binding protein 2 (SBP2) and in antioxidant defence superoxide dismutase 2 (SOD2) in relation to sporadic CRC incidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43436.RAmthp8XBls84SAZWLLRzUaruTCHDLpJp96Tkhe47kGzA130_provenance.
- NP43439.RAskFr9i1EZjiXcR79CtBsHOY53aFVuehfasG3TT-BP0Q130_assertion description "[Sequence variants of the gene encoding chemoattractant receptor expressed on Th2 cells (CRTH2) are associated with asthma and differentially influence mRNA stability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43439.RAskFr9i1EZjiXcR79CtBsHOY53aFVuehfasG3TT-BP0Q130_provenance.
- NP43443.RAoIxCsxigWcOI9vTWKTHmsxihiqGkNvi0r0hnDGEqMZg130_assertion description "[We genotyped men with localized/regional prostate cancer for 26 loci across eight genes that are central to cellular antioxidant defence: glutathione peroxidase (GPX1, GPX4), peroxisome proliferator-activated receptor coactivator (PPARGC1A, PPARGC1B), SOD1, SOD2, and SOD3, and 'X-ray repair complementing defective repair in Chinese hamster cell 1' (XRCC1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43443.RAoIxCsxigWcOI9vTWKTHmsxihiqGkNvi0r0hnDGEqMZg130_provenance.
- NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_assertion description "[In conclusion, mutations in the MCH receptors are not commonly found in humans with severe early onset obesity. Clarification of the relationship of these variants to obesity must await study in other populations and/or in genetically modified mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43445.RAuNn8G8Q8hP1cI9SYmrZF3i47e-jBCUZ_YyJE3j3qST0130_provenance.
- NP43446.RAqETIJx7VJaFLbW8CoejjI0N6G0WguKdVeRGp8EErq6c130_assertion description "[Association of melanin-concentrating hormone receptor 1 5' polymorphism with early-onset extreme obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43446.RAqETIJx7VJaFLbW8CoejjI0N6G0WguKdVeRGp8EErq6c130_provenance.
- NP43452.RAjb2qAh_r9448qjbjKfvW7BYFnglNwr8FxgMOvM-w_ek130_assertion description "[In view of previous studies linking the presence of the Pl allele of GPIIIa to a higher risk for coronary artery thrombosis, our data have physiologic relevance. However, they need to be confirmed in a larger study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43452.RAjb2qAh_r9448qjbjKfvW7BYFnglNwr8FxgMOvM-w_ek130_provenance.
- NP43464.RAhRImNAkxZxJVS_wPJtUcKSWo4w2ZkMThdd2li1Gy9nY130_assertion description "[Gene polymorphism of platelet glycoprotein I balpha in Chinese patients with large- and small-artery subtypes of ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43464.RAhRImNAkxZxJVS_wPJtUcKSWo4w2ZkMThdd2li1Gy9nY130_provenance.
- NP43472.RAp7GERfu81N7vVxmPUkbC8w6ufCaoQR_8w1iMXnPZel4130_assertion description "[Nonsense mutation and truncated GP Ib alpha polypeptide were found to cosegregate in four individuals through three generations and were associated with either Bernard-Soulier syndrome or carrier state phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43472.RAp7GERfu81N7vVxmPUkbC8w6ufCaoQR_8w1iMXnPZel4130_provenance.
- NP43481.RAsBceFAxCoD5Tf7uQDTx3Bslt1FiQEwFgcxAg8hdxiiQ130_assertion description "[To investigate the relationship between the alpha-adducin (ADD1) gene G460W and the G-protein beta 3-subunit (GNB3) gene C825T polymorphisms and essential hypertension (EH) in a northern Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43481.RAsBceFAxCoD5Tf7uQDTx3Bslt1FiQEwFgcxAg8hdxiiQ130_provenance.
- NP43490.RAgAi3GqvBigi7vymXqEqRP4o2Wzs9rVZowQI5ZydD3eI130_assertion description "[Our data suggest that the FAS 1377G>A and IL10 592C>A polymorphisms could modify disease-free and overall survival in women with lymph node-positive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43490.RAgAi3GqvBigi7vymXqEqRP4o2Wzs9rVZowQI5ZydD3eI130_provenance.
- NP43493.RAgZfyDYwd4xmrB_OsoUY8EJeFPpsdthaMbUkv3dIF74k130_assertion description "[Genetic association study of the GNB3 C825T, the ACE I/D and the eNOS G894T polymorphisms and the risk to develop erectile dysfunction in a German ED population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43493.RAgZfyDYwd4xmrB_OsoUY8EJeFPpsdthaMbUkv3dIF74k130_provenance.
- NP43497.RAprYbnbXH6Y7LI5IGlmMR73anr6YITMjKtQovmOTAIj0130_assertion description "[These differential pharmacogenetic predictors of antidepressant response by age, may provide clues to understanding the discontinuities in pharmacological responsiveness of child/adolescent and adult depressive disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43497.RAprYbnbXH6Y7LI5IGlmMR73anr6YITMjKtQovmOTAIj0130_provenance.
- NP43503.RAlO0DWGhB-t9WJiQcL7vOX_Ah17mmkGdW282nxAzKHVM130_assertion description "[We investigated whether the C825T polymorphism of the beta3 subunit of G protein (GNB3) gene is associated with the symptom severity or treatment response of major depressive disorders (MDDs) in a Korean sample of 106 MDD patients; our study also included 133 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43503.RAlO0DWGhB-t9WJiQcL7vOX_Ah17mmkGdW282nxAzKHVM130_provenance.
- NP43509.RAh6kve01j7r5mxy4UgUhtx4PmsMIv3NFgVqRAH0N7anQ130_assertion description "[ The study provided evidence against the major impact of the GNB3 C825T polymorphism on the increased risk of the development of nephropathy or hypertension in type 2 diabetic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43509.RAh6kve01j7r5mxy4UgUhtx4PmsMIv3NFgVqRAH0N7anQ130_provenance.
- NP43511.RArUK_1mjx4pimA71kXKmx-A-bhn889vnrfdvZsNld08U130_assertion description "[The risk of diabetes due to thiazide use was not increased among AGTR1 1166 CC homozygous subjects and less increased among GNB3 T allele carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43511.RArUK_1mjx4pimA71kXKmx-A-bhn889vnrfdvZsNld08U130_provenance.
- NP43518.RAvFwSTGi61l-8TlFhjPyYiqx9UdntTA_pCus4iP_yE7o130_assertion description "[Despite the small sample size, this novel analysis method identified an sMRI component including brain areas previously reported to be abnormal in schizophrenia and an associated genetic component containing several putative schizophrenia risk genes. Thus, we identified multiple genes potentially underlying specific structural brain abnormalities in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43518.RAvFwSTGi61l-8TlFhjPyYiqx9UdntTA_pCus4iP_yE7o130_provenance.
- NP43519.RAttgE_TByz_UXM7gLFiREcs0nGAOBxe_eSCg96Knrc20130_assertion description "[Preliminary results showed no statistical relationship between the C825T polymorphism and olanzapine response or weight gain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43519.RAttgE_TByz_UXM7gLFiREcs0nGAOBxe_eSCg96Knrc20130_provenance.
- NP43525.RAvJrcAG_0NnuxJl_rS9VEJ_zSSZvDua1lD_8kPgliuUo130_assertion description "[Our findings suggest that HTR5A gene could play an important role in the pathogenesis of bipolar disorder in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43525.RAvJrcAG_0NnuxJl_rS9VEJ_zSSZvDua1lD_8kPgliuUo130_provenance.
- NP43534.RAp3aAPzFis3nZk3uvGOvhh32OfRUexoUQ5JvTNcufgAw130_assertion description "[Association analysis of the functional Ala111Glu polymorphism of the glyoxalase I gene in panic disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43534.RAp3aAPzFis3nZk3uvGOvhh32OfRUexoUQ5JvTNcufgAw130_provenance.
- NP43536.RAioNIt31cWJ9nFPcg5JdKJtkO3HUJ-UWUcTnAinrAxNc130_assertion description "[Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset GLA mutation c.936+919G>A (IVS4+919G>A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43536.RAioNIt31cWJ9nFPcg5JdKJtkO3HUJ-UWUcTnAinrAxNc130_provenance.
- NP43538.RAnU9i3-3c1m-A2sPHZLC8qeGFYBzROU3n1cAkbSsuYjI130_assertion description "[These findings strengthen the importance of genetic diagnosis, providing early treatment, and genetic counseling of deaf patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43538.RAnU9i3-3c1m-A2sPHZLC8qeGFYBzROU3n1cAkbSsuYjI130_provenance.
- NP43540.RAi_sHrqxe0ce6Tg3IZWnozaulQ8mdvlINJj4pPHjg0WQ130_assertion description "[Based on these results, we are now assessing GJB6 deletion status in cases of prelingual hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43540.RAi_sHrqxe0ce6Tg3IZWnozaulQ8mdvlINJj4pPHjg0WQ130_provenance.
- NP43541.RAiLWFIuAOfSbb6i74N5W6etJf-PJGVLzwB2CmD7zdpMM130_assertion description "[Our results suggest that GJB2 and SLC26A4 mutations together make up a major cause of congenital hearing loss in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43541.RAiLWFIuAOfSbb6i74N5W6etJf-PJGVLzwB2CmD7zdpMM130_provenance.
- NP43545.RAlarv8k3MSj3HwXMUCdRtaeBJ603S12NBhJ9D73R-i6E130_assertion description "[Screening for the GJB2 c.-3170 G>A (IVS 1+1 G>A) mutation in Brazilian deaf individuals using multiplex ligation-dependent probe amplification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43545.RAlarv8k3MSj3HwXMUCdRtaeBJ603S12NBhJ9D73R-i6E130_provenance.