Nanopublications

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

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NP43196.RA2mukb1d1OT4nH3NDYZzr_NU6Kt6ZIzRxNNpnOsS3Aw4130_assertion description "[We present an investigation of joint genetic and clinical factors associated with atherosclerosis that shows predictive results for both cases, as well as enhanced performance for their combination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43196.RA2mukb1d1OT4nH3NDYZzr_NU6Kt6ZIzRxNNpnOsS3Aw4130_provenance.
NP43200.RA2temjgKW_xWZw2iiGZz-4py0ys9F6Z6G2RmAW9Rlz1I130_assertion description "[Glutathione-S-transferase genotypes, smoking, and their association with markers of inflammation, hemostasis, and endothelial function: the atherosclerosis risk in communities (ARIC) study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43200.RA2temjgKW_xWZw2iiGZz-4py0ys9F6Z6G2RmAW9Rlz1I130_provenance.
NP43201.RAx98EdroZP4l4ZkDV7MGlrjLJO5H2U__bUvYCQymOM34130_assertion description "[Effects of arsenic exposure and genetic polymorphisms of p53, glutathione S-transferase M1, T1, and P1 on the risk of carotid atherosclerosis in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43201.RAx98EdroZP4l4ZkDV7MGlrjLJO5H2U__bUvYCQymOM34130_provenance.
NP43202.RAyAjgE8UhSz0bn1ULs9C5-Qo4BEgf-Vgr_dB-ZcI3Y0c130_assertion description "[Two common deletion polymorphisms of GSTM1 and GSTT1 genes and the GSTP1 Ile105Val polymorphism have been associated with asthma in children and adults, but results are inconsistent across studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43202.RAyAjgE8UhSz0bn1ULs9C5-Qo4BEgf-Vgr_dB-ZcI3Y0c130_provenance.
NP43204.RAxn5p2e_-7lqURe_oFPmvEj0HmglIB8PD2vwWWc7flx8130_assertion description "[We examined asthma prevalence and evaluated polymorphisms in genes involved in oxidative stress pathways gluthatione S-transferases M1 (GSTM1), T1 (GSTT1), and P1 (GSTP1) and NAD(P)H:quinine oxidoreductase (NQO1), inflammatory response tumor necrosis factor alpha (TNFA), immunologic response Toll-like receptor 4 (TLR4), and airway reactivity adrenergic receptor beta2 (ADRB2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43204.RAxn5p2e_-7lqURe_oFPmvEj0HmglIB8PD2vwWWc7flx8130_provenance.
NP43205.RA2ocX04VVqND7qW3JQ2AxOJc9XQIIR705QULEe_f4ekU130_assertion description "[The glutathione S-transferase M1 (GSTM1)-null variant is a common copy number variant associated with adverse pulmonary outcomes, including asthma and airflow obstruction, with evidence of important gene-by-environment interactions with exposures to oxidative stress.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43205.RA2ocX04VVqND7qW3JQ2AxOJc9XQIIR705QULEe_f4ekU130_provenance.
NP43207.RA2Fnh0mbaOJSqHaVD7-VMH9QqliKOeJNKqS7vOH8el6I130_assertion description "[The effect of GSTM1 null/present genotype on the association between GSTP1 Ile105Val and asthma was also investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43207.RA2Fnh0mbaOJSqHaVD7-VMH9QqliKOeJNKqS7vOH8el6I130_provenance.
NP43208.RAxMfvrNlwXbbnjx7l7vMc28P7MpEZmfSWXO6YUTzBfig130_assertion description "[The GSTM1 null genotype was found to be protective from the development of asthma in atopic subjects (odds ratios 0.55, 95% confidence interval 0.34-0.90; P=0.017).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43208.RAxMfvrNlwXbbnjx7l7vMc28P7MpEZmfSWXO6YUTzBfig130_provenance.
NP43221.RAzCvob6gblnSBM7gH-a80Yo8VgXsp4ESSA0GqzithuiY130_assertion description "[It is suggested that NAT2 slow-acetylator, GSTM1 null, GSTM1/GSTT1-double null, and variant CYP2A6 genotypes may play important roles in the development of bladder cancer in Henan area, China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43221.RAzCvob6gblnSBM7gH-a80Yo8VgXsp4ESSA0GqzithuiY130_provenance.
NP43223.RA2-iIfPg96LKjnUK2bUZuD3yF4QjECrYQOFgLXtcVkQ8130_assertion description "[This study suggests that in Tunisian subjects the GSTM1 null genotype may be associated with an increased risk of bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43223.RA2-iIfPg96LKjnUK2bUZuD3yF4QjECrYQOFgLXtcVkQ8130_provenance.
NP43224.RA9eS6klIDzhyDbmgkT3wvIsDB1D_SAENm1A71_GpIGe8130_assertion description "[In summary, these prospective results are consistent with previous literature supporting associations between bladder cancer and the NAT2 slow acetylation and the GSTM1 null genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43224.RA9eS6klIDzhyDbmgkT3wvIsDB1D_SAENm1A71_GpIGe8130_provenance.
NP43226.RA_CGIGCdOsZPbyYMoFEAWauE9hzAzMfUgIJnZKQNwYkY130_assertion description "[Glutathione S-transferase M1, T1 and P1 polymorphisms and bladder cancer risk in Egyptians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43226.RA_CGIGCdOsZPbyYMoFEAWauE9hzAzMfUgIJnZKQNwYkY130_provenance.
NP43229.RA7BZwxjj3F9oeUeZCerOdbMNbF8Nh0OqqHmtiE8roY6E130_assertion description "[ The functional GSTT-1*A genotype was associated with severe attacks of pancreatitis. Heightened oxidative stress characterized by glutathione depletion may be of importance in mediating the progression from mild to severe pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43229.RA7BZwxjj3F9oeUeZCerOdbMNbF8Nh0OqqHmtiE8roY6E130_provenance.
NP43236.RA3Wu9ZL8JYkFfOvyhs0NYU6_Aw2GiIHdib-jrWhVr3n4130_assertion description "[ Further study of the role of the AhR polymorphism is warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43236.RA3Wu9ZL8JYkFfOvyhs0NYU6_Aw2GiIHdib-jrWhVr3n4130_provenance.
NP43240.RA08YXUeUhx_iFf2GT7kRuP2YFSziF3JAtAzwJ0YUWjEU130_assertion description "[These results suggest that the GSTT1 null genotype may be associated with increased risk of stomach cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43240.RA08YXUeUhx_iFf2GT7kRuP2YFSziF3JAtAzwJ0YUWjEU130_provenance.
NP43244.RA4dzhlSwi_mcA337F1vFQ2qJV0Dy3haQiljfvACEdNFQ130_assertion description "[Specific polymorphisms may influence clinical outcomes of AGC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43244.RA4dzhlSwi_mcA337F1vFQ2qJV0Dy3haQiljfvACEdNFQ130_provenance.
NP43246.RA0qy9dI3Z9XDBMZ1-E4KIDQ4Xmu1jzltnx-cXdgVsUbA130_assertion description "[Polymorphisms in detoxification genes CYP1A1, CYP2E1, GSTT1 and GSTM1 in gastric cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43246.RA0qy9dI3Z9XDBMZ1-E4KIDQ4Xmu1jzltnx-cXdgVsUbA130_provenance.
NP43248.RA-6igq-MkucNFPOPrWIE0rt4wtNiNT54BuOAAx0eMJVQ130_assertion description "[A case-control study was performed in 303 subjects (108 GC and 195 healthy controls) to analyze the association of polymorphisms in GSTM1, GSTT1, GSTP1, GSTM3, CYP1A1, and CYP2E1 genes in susceptibility to GC in Kashmir Valley.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43248.RA-6igq-MkucNFPOPrWIE0rt4wtNiNT54BuOAAx0eMJVQ130_provenance.
NP29852.RAnUgEe0a19CgiGhasyT6t4tMaLLAad44iAy8R54ZXreo130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29852.RAnUgEe0a19CgiGhasyT6t4tMaLLAad44iAy8R54ZXreo130_provenance.
NP29864.RAoDIhoUlWBEwIByfg5bCaQVNOidTUuHk-BSaybcn3hZ0130_assertion description "[Chronic hyperglycemia, independent of plasma lipid levels, is sufficient for the loss of beta-cell differentiation and secretory function in the db/db mouse model of diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29864.RAoDIhoUlWBEwIByfg5bCaQVNOidTUuHk-BSaybcn3hZ0130_provenance.
NP29865.RAldr5FfgWbaO-762LLZKbB7SyvjQwHEhEmWVaKT_43Hc130_assertion description "[Chronic hyperglycemia, independent of plasma lipid levels, is sufficient for the loss of beta-cell differentiation and secretory function in the db/db mouse model of diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29865.RAldr5FfgWbaO-762LLZKbB7SyvjQwHEhEmWVaKT_43Hc130_provenance.
NP29869.RAptAclMUna5ah453V1uQScZmC7C_IpCvJqa-Er4q4E60130_assertion description "[Microarray analyses in dendritic cells reveal potential biomarkers for chemical-induced skin sensitization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29869.RAptAclMUna5ah453V1uQScZmC7C_IpCvJqa-Er4q4E60130_provenance.
NP29870.RAhEmYKpWREvyB7MCVRvdV9bkzD9nRbDW-zINZt2H8png130_assertion description "[A toxicogenomic approach to drug-induced phospholipidosis: analysis of its induction mechanism and establishment of a novel in vitro screening system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29870.RAhEmYKpWREvyB7MCVRvdV9bkzD9nRbDW-zINZt2H8png130_provenance.
NP29874.RAjblyGKpFC-IUZ270W8pahxrQ-GteATEC8cm-q669L0k130_assertion description "[Impaired expression of NADH dehydrogenase subunit 1 and PPARgamma coactivator-1 in skeletal muscle of ZDF rats: restoration by troglitazone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29874.RAjblyGKpFC-IUZ270W8pahxrQ-GteATEC8cm-q669L0k130_provenance.
NP29880.RAnIC9_CBxr4h04oUDVGokPoxtQQOs8yAJhJO2phu4wkY130_assertion description "[Troglitazone improves GLUT4 expression in adipose tissue in an animal model of obese type 2 diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29880.RAnIC9_CBxr4h04oUDVGokPoxtQQOs8yAJhJO2phu4wkY130_provenance.
NP29886.RAtBMHuwKgnuIYhyVjAJ5JoGvKUF9M4dX-IsD6Eg2RWcE130_assertion description "[Mutations in the SLC2A9 gene cause hyperuricosuria and hyperuricemia in the dog.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29886.RAtBMHuwKgnuIYhyVjAJ5JoGvKUF9M4dX-IsD6Eg2RWcE130_provenance.
NP29888.RAtBlFm411DoRip8X-O2A_irTPoPzv-LuR-tqrsGtdBGY130_assertion description "[Expression profiles of hippocampal regenerative sprouting-related genes and their regulation by E-64d in a developmental rat model of penicillin-induced recurrent epilepticus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29888.RAtBlFm411DoRip8X-O2A_irTPoPzv-LuR-tqrsGtdBGY130_provenance.
NP29895.RAptencvJ7MuJasoSG5avepbt52wKeNv1Vk2FaYUmBeAI130_assertion description "[Beta cell-specific Znt8 deletion in mice causes marked defects in insulin processing, crystallisation and secretion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29895.RAptencvJ7MuJasoSG5avepbt52wKeNv1Vk2FaYUmBeAI130_provenance.
NP29905.RAlOATKnTSBsFPzxSp6hdL4SDD1tMio9fTgpUPia1adx0130_assertion description "[Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29905.RAlOATKnTSBsFPzxSp6hdL4SDD1tMio9fTgpUPia1adx0130_provenance.
NP29936.RAtkf2nkhrffvuAoMZYWuUHE9mOzJIRVxbk1xnoyQfjbo130_assertion description "[Here we report that mice deficient in Zn transporter Slc39a13/Zip13 show changes in bone, teeth and connective tissue reminiscent of the clinical spectrum of human Ehlers-Danlos syndrome (EDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29936.RAtkf2nkhrffvuAoMZYWuUHE9mOzJIRVxbk1xnoyQfjbo130_provenance.
NP29944.RAliYVc_kReUaAtdKgzetBzWwscGuOOP4Rh3X32bz8ZeM130_assertion description "[Identification of SLC39A4, a gene involved in acrodermatitis enteropathica.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29944.RAliYVc_kReUaAtdKgzetBzWwscGuOOP4Rh3X32bz8ZeM130_provenance.
NP29946.RAuURGBtFfIjmPCoJ6orXu-pDv1ld3F-Qe20PQ-XaaMXQ130_assertion description "[The ZIP5 gene encodes a protein closely related to ZIP4, a zinc transporter mutated in the human genetic disorder acrodermatitis enteropathica.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29946.RAuURGBtFfIjmPCoJ6orXu-pDv1ld3F-Qe20PQ-XaaMXQ130_provenance.
NP29950.RAlc421Bxa6qpgbK8sER8wAsSVmz_DI44eNpjpE1Lo8XA130_assertion description "[Anti-inflammatory effects of zinc and alterations in zinc transporter mRNA in mouse models of allergic inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29950.RAlc421Bxa6qpgbK8sER8wAsSVmz_DI44eNpjpE1Lo8XA130_provenance.
NP29970.RAunD4s_bYN7hyMIHnhEbkqt_cTR4jVJU19x2R8DAbOQQ130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29970.RAunD4s_bYN7hyMIHnhEbkqt_cTR4jVJU19x2R8DAbOQQ130_provenance.
NP29971.RAqGqU1FOxrxQ4-18LF6TgbY9XW_ylPufq0bjOmA4i7Io130_assertion description "[Genome wide association for addiction: replicated results and comparisons of two analytic approaches.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29971.RAqGqU1FOxrxQ4-18LF6TgbY9XW_ylPufq0bjOmA4i7Io130_provenance.
NP29972.RAkCM7txpFAIT5BTxeXG2LG8ZloNtZD_8HMmiF8csq55I130_assertion description "[By 4 weeks of age, PCFT-deficient (PCFT(-/-)) mice developed severe macrocytic normochromic anemia and pancytopenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29972.RAkCM7txpFAIT5BTxeXG2LG8ZloNtZD_8HMmiF8csq55I130_provenance.
NP29973.RAtusgAl_nPloz8x69RjI9MEVli8u7zrtQnZm-04fptHI130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29973.RAtusgAl_nPloz8x69RjI9MEVli8u7zrtQnZm-04fptHI130_provenance.
NP29974.RAvMMzFD8CmhWc9p5jxIOXsmIqqVMhv1ms-odSRptMWTk130_assertion description "[Genetic or nutritional disorders in homocysteine or folate metabolism increase protein N-homocysteinylation in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29974.RAvMMzFD8CmhWc9p5jxIOXsmIqqVMhv1ms-odSRptMWTk130_provenance.
NP29978.RAmmGrV2EgLyZUBCBh_dDwJ_zOIU7YmYyVeXI-qW4ogvM130_assertion description "[Mutations in the SLC4A1 gene encoding the anion exchanger 1 (AE1) can cause distal renal tubular acidosis (dRTA), a disease often due to mis-trafficking of the mutant protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29978.RAmmGrV2EgLyZUBCBh_dDwJ_zOIU7YmYyVeXI-qW4ogvM130_provenance.
NP29982.RAkyA70-ayE1U2kxa3g238nz4zS3Wau6UgyHqvGLx5Tdg130_assertion description "[Band 3 HT, a human red-cell variant associated with acanthocytosis and increased anion transport, carries the mutation Pro-868-->Leu in the membrane domain of band 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29982.RAkyA70-ayE1U2kxa3g238nz4zS3Wau6UgyHqvGLx5Tdg130_provenance.
NP29983.RArRvHyk5fxNVPvK6zpfnctg-FtE9dFM1t_f0450t94Zc130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29983.RArRvHyk5fxNVPvK6zpfnctg-FtE9dFM1t_f0450t94Zc130_provenance.
NP29987.RAu1phMQwqIATf9R4lnssKdl9RTKj7GWwd_P4mXlI31hQ130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29987.RAu1phMQwqIATf9R4lnssKdl9RTKj7GWwd_P4mXlI31hQ130_provenance.
NP29990.RArHG9viogSmpUluU5LNtEVunJiidwszVCs_4HSwIlHuw130_assertion description "[Disruption of sodium bicarbonate transporter SLC4A10 in a patient with complex partial epilepsy and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29990.RArHG9viogSmpUluU5LNtEVunJiidwszVCs_4HSwIlHuw130_provenance.
NP29995.RAnvOc5EHvC2akbOOGZUWgHppJgRLz9lu94GFbaoywIUo130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29995.RAnvOc5EHvC2akbOOGZUWgHppJgRLz9lu94GFbaoywIUo130_provenance.
NP30002.RAr6FasBg1s3S8GqTnwXQ0110YWJv0U5CW0wLy3IOUPvg130_assertion description "[Autosomal recessive proximal renal tubular acidosis is caused by mutations in the SLC4A4 gene encoding the electrogenic sodium bicarbonate cotransporter NBCe1-A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30002.RAr6FasBg1s3S8GqTnwXQ0110YWJv0U5CW0wLy3IOUPvg130_provenance.
NP30010.RArVgtBHWl3P1VPiTgnRT2FsvpWBRnW_orttI2gQjMN08130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30010.RArVgtBHWl3P1VPiTgnRT2FsvpWBRnW_orttI2gQjMN08130_provenance.
NP30017.RAtHIUcJI36cG3ro7PUF4ahUsZZ-5rNBVaYrYeJQM5I18130_assertion description "[Establishment of a human hepatocellular carcinoma cell line highly expressing sodium iodide symporter for radionuclide gene therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30017.RAtHIUcJI36cG3ro7PUF4ahUsZZ-5rNBVaYrYeJQM5I18130_provenance.
NP30018.RAtqT3GV9ztD20lRRMajhXRNOipx5EN580gXDJq9SbKZw130_assertion description "[Long-term radioiodine retention and regression of liver cancer after sodium iodide symporter gene transfer in wistar rats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30018.RAtqT3GV9ztD20lRRMajhXRNOipx5EN580gXDJq9SbKZw130_provenance.
NP30033.RAjjBLm3YdeVlEQ2azCDOwW3Kp0o7pv-7cxUGy2xjUW80130_assertion description "[Na(+)/monocarboxylate transport (SMCT) protein expression correlates with survival in colon cancer: molecular characterization of SMCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30033.RAjjBLm3YdeVlEQ2azCDOwW3Kp0o7pv-7cxUGy2xjUW80130_provenance.
NP30050.RAppAWJkXq1YuryCpxv4UidTGQ4e5EREvXXrg69gc3zDw130_assertion description "[Statistically significantly increased methylation in MM versus non-tumor lung samples was found for estrogen receptor 1 (ESR1; p = 0.0002), solute carrier family 6 member 20 (SLC6A20; p = 0.0022) and spleen tyrosine kinase (SYK; p=0.0003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30050.RAppAWJkXq1YuryCpxv4UidTGQ4e5EREvXXrg69gc3zDw130_provenance.
NP30051.RAifoFlJaX6P-VKkV2a3MpxQ7UhNLIxdX4GqcxMk3NPKg130_assertion description "[Nine- or fewer repeat alleles in VNTR polymorphism of the dopamine transporter gene is a strong risk factor for prolonged methamphetamine psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30051.RAifoFlJaX6P-VKkV2a3MpxQ7UhNLIxdX4GqcxMk3NPKg130_provenance.
NP30052.RAqm4r46NOt8Pb-2p6kxANKHCTVnkdKzO72xSXwu9A2KI130_assertion description "[Association of ADHD, tics, and anxiety with dopamine transporter (DAT1) genotype in autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30052.RAqm4r46NOt8Pb-2p6kxANKHCTVnkdKzO72xSXwu9A2KI130_provenance.
NP30055.RAtbcatpg92zHncB8kqYmiyoGLwKTSrzLOMb66wUnnInM130_assertion description "[Association of ADHD, tics, and anxiety with dopamine transporter (DAT1) genotype in autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30055.RAtbcatpg92zHncB8kqYmiyoGLwKTSrzLOMb66wUnnInM130_provenance.
NP30057.RAn0cEJvPT1_FR63HfI0HY7BEy6OQA_OXEx7sPJLc-NB4130_assertion description "[Molecular mechanisms of cocaine reward: combined dopamine and serotonin transporter knockouts eliminate cocaine place preference.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30057.RAn0cEJvPT1_FR63HfI0HY7BEy6OQA_OXEx7sPJLc-NB4130_provenance.
NP30058.RApXl8AtWRPHNmycAY4s417Pm97-b7-YHA4LGWhe3i0tI130_assertion description "[Molecular mechanisms of cocaine reward: combined dopamine and serotonin transporter knockouts eliminate cocaine place preference.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30058.RApXl8AtWRPHNmycAY4s417Pm97-b7-YHA4LGWhe3i0tI130_provenance.
NP30060.RAnCPZS5MLEBp7hF8Noo7eZ3kfB741SjgCN-Oh01miGl4130_assertion description "[Self-administration of cocaine and the cocaine analog RTI-113: relationship to dopamine transporter occupancy determined by PET neuroimaging in rhesus monkeys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30060.RAnCPZS5MLEBp7hF8Noo7eZ3kfB741SjgCN-Oh01miGl4130_provenance.
NP30061.RAvTe2hmKT3_j3r8M5L2x4IcutSacbYDs9vU4mkYT6eEw130_assertion description "[A dopamine transporter gene functional variant associated with cocaine abuse in a Brazilian sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30061.RAvTe2hmKT3_j3r8M5L2x4IcutSacbYDs9vU4mkYT6eEw130_provenance.
NP30064.RAtyU8YecoTg45Wd9WotpG_oGIUjr4H7Q4KK_ltNe4prQ130_assertion description "[Lack of cocaine self-administration in mice expressing a cocaine-insensitive dopamine transporter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30064.RAtyU8YecoTg45Wd9WotpG_oGIUjr4H7Q4KK_ltNe4prQ130_provenance.
NP30072.RAoWgyJTytBjPEiICdf2zze7v94Zr2bUz-4pgLo1gp0oY130_assertion description "[The role of dopamine transporter in selective toxicity of manganese and rotenone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30072.RAoWgyJTytBjPEiICdf2zze7v94Zr2bUz-4pgLo1gp0oY130_provenance.
NP30089.RAk76MRaR80yJlgxre-DuJt7fpIbUMrL8_vCiwZnlvApk130_assertion description "[The integrin beta3 (ITGB3) and serotonin transporter (SLC6A4) genes were both recently identified as male quantitative trait loci (QTLs) for serotonin levels and alleles of each have been associated with autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30089.RAk76MRaR80yJlgxre-DuJt7fpIbUMrL8_vCiwZnlvApk130_provenance.
NP30090.RAgDmFjyO3U5ma7oZ-8qKCBcEHxR0bmSp0sRPFDwZVSqo130_assertion description "[The overall results implicate SLC6A4 and ITGB3 gene interactions in autism etiology and in serotonin level determination, providing evidence for a common underlying genetic mechanism and a molecular explanation for the association of platelet hyperserotonemia with autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30090.RAgDmFjyO3U5ma7oZ-8qKCBcEHxR0bmSp0sRPFDwZVSqo130_provenance.
NP30092.RAif_QNCGlLcYLSA63oP7PHsZ3kew_c2hxaimAm25GF7s130_assertion description "[5-HTTLPR polymorphism: analysis in South African autistic individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30092.RAif_QNCGlLcYLSA63oP7PHsZ3kew_c2hxaimAm25GF7s130_provenance.
NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_assertion description "[Relative to the comparison subjects, subjects with bipolar disorder without panic disorder, but not those with comorbid bipolar disorder and panic disorder, showed significantly higher frequencies of the COMT Met158 and the short 5-HTTLPR alleles and genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30094.RAo6x5qwdo55U9AqaFShAbaMGpE0bftTclWYsiYurxAmQ130_provenance.
NP30097.RAkCCW-WRE12D3108kd4sbMEmkXfEMv04BPKvW5u5ktZg130_assertion description "[5-HTTLPR and early childhood adversities moderate cognitive and emotional processing in adolescence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30097.RAkCCW-WRE12D3108kd4sbMEmkXfEMv04BPKvW5u5ktZg130_provenance.
NP30104.RAhSGrxQuy6xjjg7thqJ30OR_vnP3cTNhnght-5tHr3rE130_assertion description "[These findings suggest that within this restricted population increased symptoms of depression, anxiety, and memory are associated with the 5-HTTLPR polymorphism among both males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30104.RAhSGrxQuy6xjjg7thqJ30OR_vnP3cTNhnght-5tHr3rE130_provenance.
NP30114.RAtZA6SDl2Pg01T2kRz2r55u0oPaSMKLBAlqIW3OxpMd0130_assertion description "[Screening of male patients with autism spectrum disorder for creatine transporter deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30114.RAtZA6SDl2Pg01T2kRz2r55u0oPaSMKLBAlqIW3OxpMd0130_provenance.
NP30117.RAgZK9g3JWCa-5nmvzZqTZhRIzBcvjJl6uB0QYKcBCZo4130_assertion description "[Functional characterization of missense variants in the creatine transporter gene (SLC6A8): improved diagnostic application.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30117.RAgZK9g3JWCa-5nmvzZqTZhRIzBcvjJl6uB0QYKcBCZo4130_provenance.
NP30118.RAjyZm1Qm4TL0PwlZHl-Doy-iviKL5n1OQG1dxkztEgXU130_assertion description "[We report the first X-linked creatine-deficiency syndrome caused by a defective creatine transporter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30118.RAjyZm1Qm4TL0PwlZHl-Doy-iviKL5n1OQG1dxkztEgXU130_provenance.
NP30123.RAqskz3LbtXdvhvtpON17q_mTXI4gYtLUDqsy7S0EFk74130_assertion description "[Microarray analyses in dendritic cells reveal potential biomarkers for chemical-induced skin sensitization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30123.RAqskz3LbtXdvhvtpON17q_mTXI4gYtLUDqsy7S0EFk74130_provenance.
NP30124.RAmuuwyzYOp9XNBwFD3-Hd704-ZUKkhZoZTAmI1pRZ_c0130_assertion description "[Vascular endothelial dysfunction resulting from L-arginine deficiency in a patient with lysinuric protein intolerance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30124.RAmuuwyzYOp9XNBwFD3-Hd704-ZUKkhZoZTAmI1pRZ_c0130_provenance.
NP30127.RAgNgwYpYQEET1hWDNESaRu7uajA7zfUxUcPT1iAvA9Hg130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30127.RAgNgwYpYQEET1hWDNESaRu7uajA7zfUxUcPT1iAvA9Hg130_provenance.
NP30128.RAm1KMl7t1xamYHg2_syVmEd98TgoYZoVJD4uxtJ4Sklg130_assertion description "[Variants at three of these loci have previously been linked with important clinical outcomes: SLC7A9 is a risk locus for chronic kidney disease, NAT2 for coronary artery disease and genotype-dependent response to drug toxicity, and SLC6A20 for iminoglycinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30128.RAm1KMl7t1xamYHg2_syVmEd98TgoYZoVJD4uxtJ4Sklg130_provenance.
NP30129.RAk2bosWwzaSTi2psF-YvkTX7tH_KsnxO7WrQ4-K6r5Ww130_assertion description "[Acetylcholine-related bowel dysmotility in homozygous mutant NCX/HOX11L.1-deficient (NCX-/-) mice-evidence that acetylcholine is implicated in causing intestinal neuronal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30129.RAk2bosWwzaSTi2psF-YvkTX7tH_KsnxO7WrQ4-K6r5Ww130_provenance.
NP30133.RAkxkIym1gddOvmAAPL0LOLMebyCHp2rTgKGUv3Ti6K5Q130_assertion description "[Here we further investigated the role of NCX in the etiology of seizures by quantifying the effects of KB-R7943 and SN-6, potent inhibitors of the reverse mode of NCX subtypes 3 (NCX3) and 1 (NCX1), respectively, on the occurrence of acute seizures and status epilepticus induced by intraperitoneal administration of pilocarpine, a muscarinic acetylcholine receptor agonist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30133.RAkxkIym1gddOvmAAPL0LOLMebyCHp2rTgKGUv3Ti6K5Q130_provenance.
NP30140.RAieaaeQ4Kj-PyB3hF31DA-K1gP4yhqQPTXMpB2N9pPB8130_assertion description "[Sodium hydrogen exchanger as a mediator of hydrostatic edema-induced intestinal contractile dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30140.RAieaaeQ4Kj-PyB3hF31DA-K1gP4yhqQPTXMpB2N9pPB8130_provenance.
NP30142.RArmseOB8J2ogeapJc0Sf3SOeVZ5e-lK4GomRD7LjP2WE130_assertion description "[Identification of the Na+/H+ exchanger 1 in dorsal root ganglion and spinal cord: its possible role in inflammatory nociception.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30142.RArmseOB8J2ogeapJc0Sf3SOeVZ5e-lK4GomRD7LjP2WE130_provenance.
NP30147.RAliRH2gYCXReNWqSkNzJYl0nF6KBrAS-4vRGezAYzVcI130_assertion description "[Effect of potent redox-modulating manganese porphyrin, MnTM-2-PyP, on the Na(+)/H(+) exchangers NHE-1 and NHE-3 in the diabetic rat.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30147.RAliRH2gYCXReNWqSkNzJYl0nF6KBrAS-4vRGezAYzVcI130_provenance.
NP30159.RAvh7wknCCKqPqiPrS-lhx_V80kEX5Os5xu1wXh-8jPK0130_assertion description "[However, when subjects were stratified by statin type, the SLCO1B1 rs4149056 genotype was significantly associated with myopathy in patients who received simvastatin, but not in patients who received atorvastatin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30159.RAvh7wknCCKqPqiPrS-lhx_V80kEX5Os5xu1wXh-8jPK0130_provenance.
NP30163.RApfr2RBk-Tp3NiypXG8OPqSXaZkwwugZw5S29Q-tx2IY130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30163.RApfr2RBk-Tp3NiypXG8OPqSXaZkwwugZw5S29Q-tx2IY130_provenance.
NP30165.RArUQq41UZU_4-w33Do8B2tR7LNDvJ2iPClbWTUt4YY1k130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30165.RArUQq41UZU_4-w33Do8B2tR7LNDvJ2iPClbWTUt4YY1k130_provenance.
NP30167.RAurKd0R1ZGpUnCWNPu4VX0FrAfKoxL-f3lqYbHaMEo_w130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30167.RAurKd0R1ZGpUnCWNPu4VX0FrAfKoxL-f3lqYbHaMEo_w130_provenance.
NP30174.RAumHBhI_iNqRgImBk1tjYpkX0Q9AF2PHgiCFlBhZelj4130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30174.RAumHBhI_iNqRgImBk1tjYpkX0Q9AF2PHgiCFlBhZelj4130_provenance.
NP30175.RAl_KOuoiimjpEej0tKx9AQXY4Q0MW_GOF7Erw5pTbvtI130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30175.RAl_KOuoiimjpEej0tKx9AQXY4Q0MW_GOF7Erw5pTbvtI130_provenance.
NP30177.RAiz3Ln3TZ8v7WjICODQKn9K0KyGsZmR0-tqvWk7a3VKk130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30177.RAiz3Ln3TZ8v7WjICODQKn9K0KyGsZmR0-tqvWk7a3VKk130_provenance.
NP30178.RArcCcrXX5XGqaoWIAyQFh9o149YW25HOWzh3BeyEcAyI130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30178.RArcCcrXX5XGqaoWIAyQFh9o149YW25HOWzh3BeyEcAyI130_provenance.
NP30179.RAizD_HZylrOjbYHqx3tMmM632YioZcEe1c7pFScpYs6c130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30179.RAizD_HZylrOjbYHqx3tMmM632YioZcEe1c7pFScpYs6c130_provenance.
NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_assertion description "[Moreover, overexpression of SLIT2 in SMMC-7721 cells induced by recombinant adenovirus suppressed cell growth, migration, and invasion, These results suggest that epigenetic inactivation of SLIT2 in HCC may be important in the development and progression of HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30181.RAgfwk26umvlX6CRgyNI5iBvqTZ4Moez4FV69J5lblrxU130_provenance.
NP30188.RAjKxbj3WGqQfJaZKEBSIYnytipbsYDrgGYeY-srIRJVg130_assertion description "[Genome wide association for addiction: replicated results and comparisons of two analytic approaches.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30188.RAjKxbj3WGqQfJaZKEBSIYnytipbsYDrgGYeY-srIRJVg130_provenance.
NP30190.RAvk2OpZGzSHRwLzgcqqrBxaBEQHmrZthRXSVS8IZ8dZE130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30190.RAvk2OpZGzSHRwLzgcqqrBxaBEQHmrZthRXSVS8IZ8dZE130_provenance.
NP30191.RAgQmLRHNGy_axzOxJjXDRCM6pO_JGZ3PixxEPGTsDdvI130_assertion description "[Different transcriptional control of metabolism and extracellular matrix in visceral and subcutaneous fat of obese and rimonabant treated mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30191.RAgQmLRHNGy_axzOxJjXDRCM6pO_JGZ3PixxEPGTsDdvI130_provenance.
NP30192.RAu6LeaQv5lV8ALIvusMUABCTivgXn6rzLS1Kk-iDeMhM130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30192.RAu6LeaQv5lV8ALIvusMUABCTivgXn6rzLS1Kk-iDeMhM130_provenance.
NP30194.RAlnTpRbU2x9IIYzkHO0vebhtF_t_Hx9TdiMQLDst1jFI130_assertion description "[Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30194.RAlnTpRbU2x9IIYzkHO0vebhtF_t_Hx9TdiMQLDst1jFI130_provenance.
NP30205.RAkEz0qSmmjQfrq_tvrHmZZykQHfeu0wOOvYc6gSBClnM130_assertion description "[Smad2 and Smad3 coordinately regulate craniofacial and endodermal development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30205.RAkEz0qSmmjQfrq_tvrHmZZykQHfeu0wOOvYc6gSBClnM130_provenance.
NP30206.RAvizVO4RrGwyp6sxJNYihdauGReWZKQu6cycyAo55XNY130_assertion description "[Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30206.RAvizVO4RrGwyp6sxJNYihdauGReWZKQu6cycyAo55XNY130_provenance.
NP30207.RAtYREastZf4IT1DfE6sXdd7AQeI1GudawZc5KggR0QsU130_assertion description "[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30207.RAtYREastZf4IT1DfE6sXdd7AQeI1GudawZc5KggR0QsU130_provenance.
NP30209.RAn6cyFYDycX-Tm1k9VNUApAwfe3w4VtsixbLQKnyqY6M130_assertion description "[Protective effect of genistein isolated from Hydrocotyle sibthorpioides on hepatic injury and fibrosis induced by chronic alcohol in rats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30209.RAn6cyFYDycX-Tm1k9VNUApAwfe3w4VtsixbLQKnyqY6M130_provenance.
NP30211.RAsVi6S5tFdBhP0euUeG1nr9uqhTTPrUCSrDexfYvoXtk130_assertion description "[Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30211.RAsVi6S5tFdBhP0euUeG1nr9uqhTTPrUCSrDexfYvoXtk130_provenance.
NP30213.RAnYycF8p5ae2lvn6y91YEoOaxpBcZHbfuxjqTx7i5eaQ130_assertion description "[Effects of angiotensin converting enzyme inhibitor, angiotensin II type I receptor blocker and their combination on postinfarcted ventricular remodeling in rats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30213.RAnYycF8p5ae2lvn6y91YEoOaxpBcZHbfuxjqTx7i5eaQ130_provenance.
NP30217.RAgsV-jhHJXQ8BpjjCu2iAKSWxWVJ0LsCtPQ3NDkcekeI130_assertion description "[Exome sequencing of liver fluke-associated cholangiocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30217.RAgsV-jhHJXQ8BpjjCu2iAKSWxWVJ0LsCtPQ3NDkcekeI130_provenance.
NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_assertion description "[We identified three distinct heterozygous missense SMAD4 mutations affecting the codon for Ile500 in 11 individuals with Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_provenance.

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