Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP51252.RAubymaxyhvxVCiGujD8pZMxw78n3M-OXYDCii9aC-BqM130_assertion description "[The results showed that the alpha-synuclein gene is associated with sporadic AD in women, independent of ApoE epsilon4 status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51252.RAubymaxyhvxVCiGujD8pZMxw78n3M-OXYDCii9aC-BqM130_provenance.
- NP51254.RAia9hG-5o6aQiTirGDJQiB2tIbc5H0pQsv5A8B4C4Ju4130_assertion description "[ Mutations in the beta-synuclein gene may predispose to DLB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51254.RAia9hG-5o6aQiTirGDJQiB2tIbc5H0pQsv5A8B4C4Ju4130_provenance.
- NP51259.RAuWasXrFhIH1IxtykKN3-pcgyCH3qpg5Ojnjz3OQVtDs130_assertion description "[Association study of a SNAP-25 microsatellite and attention deficit hyperactivity disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51259.RAuWasXrFhIH1IxtykKN3-pcgyCH3qpg5Ojnjz3OQVtDs130_provenance.
- NP51263.RAgJLGzDnfrGcU4pZ4VkqkA4N8mSHFoelQJMuMs0RTFFE130_assertion description "[Investigation of parent-of-origin effects in ADHD candidate genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51263.RAgJLGzDnfrGcU4pZ4VkqkA4N8mSHFoelQJMuMs0RTFFE130_provenance.
- NP51267.RAj48ookiTpJEk4B8rYqjdnOknme_Sc5CcbEAeb3ZcUR4130_assertion description "[The results from the genome-wide single nucleotide polymorphism array analysis suggest that INI1 is the primary tumor suppressor gene involved in the development of rhabdoid tumors with no second locus identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51267.RAj48ookiTpJEk4B8rYqjdnOknme_Sc5CcbEAeb3ZcUR4130_provenance.
- NP51270.RAonvUZtyOT4jv3oEXK63_XoLFw74LOZpNd-2_n7R5qlQ130_assertion description "[Mutation screening in juvenile polyposis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51270.RAonvUZtyOT4jv3oEXK63_XoLFw74LOZpNd-2_n7R5qlQ130_provenance.
- NP51273.RAmx2A0pQnBx9k1x8Musau1nC7PFEfJ6Bvk4mEKfvTPP4130_assertion description "[We sequenced the entire SLITRK1 gene including the coding region the 5' and 3' untranslated region in 92 Austrian patients with TD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51273.RAmx2A0pQnBx9k1x8Musau1nC7PFEfJ6Bvk4mEKfvTPP4130_provenance.
- NP51275.RAqlArlOGNiCpU6yNQFI0YWM0uLKsdBSy-4OKCQRF2Y0c130_assertion description "[Frequent epigenetic inactivation of the SLIT2 gene in gliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51275.RAqlArlOGNiCpU6yNQFI0YWM0uLKsdBSy-4OKCQRF2Y0c130_provenance.
- NP51277.RAma-TPnh7Nkfg3byMBNvO33ZY6-gHGG5sABuefpNvQ_A130_assertion description "[Amongst hyperbilirubinemic adults, bilirubin values tended to parallel variation status of their haplotypes. Adults featuring certain haplotypes in UGT1A1, OATP2 and G6PD genes face a high risk of developing unconjugated hyperbilirubinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51277.RAma-TPnh7Nkfg3byMBNvO33ZY6-gHGG5sABuefpNvQ_A130_provenance.
- NP51279.RAsOtFzcJEDnhq55GeTqjlZN4qGgwND6Nb_Yh84SO35go130_assertion description "[ Thr 663Ala polymorphism of alpha-ENaC gene may be a genetic risk of ischemic stroke in Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51279.RAsOtFzcJEDnhq55GeTqjlZN4qGgwND6Nb_Yh84SO35go130_provenance.
- NP51282.RAvLLcmG5D6sxv62bkHv319WFm7c0gfL9bmgSOSbCCggQ130_assertion description "[Thus, our study suggests that NCX1 is one of the genes related to susceptibility to essential hypertension in the Japanese general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51282.RAvLLcmG5D6sxv62bkHv319WFm7c0gfL9bmgSOSbCCggQ130_provenance.
- NP51286.RAjgEiydGbMVKDamp2JDzRHVpnDGZThlXh6lABO3Yucwk130_assertion description "[164 probands from the International Cystinuria Consortium were screened for mutations in SLC3A1 (type A) and SLC7A9 (type B) and classified on the basis of urine excretion of cystine and dibasic amino acids by obligate heterozygotes into 37 type I (silent heterozygotes), 46 type non-I (hyperexcretor heterozygotes), 14 mixed, and 67 untyped probands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51286.RAjgEiydGbMVKDamp2JDzRHVpnDGZThlXh6lABO3Yucwk130_provenance.
- NP51288.RAggGgSghgmBnmKQXCeg7I4zRMONyGaiPkkY_7uKM2weE130_assertion description "[Comparison between SLC3A1 and SLC7A9 cystinuria patients and carriers: a need for a new classification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51288.RAggGgSghgmBnmKQXCeg7I4zRMONyGaiPkkY_7uKM2weE130_provenance.
- NP51293.RAoUazrixLfnVnLjrEH5z6o4RSBYSP1dUwNE7tyTuVTU4130_assertion description "[Genes involved in the transmission, reuptake and metabolism of serotonin constitute a set of candidate genes that could be involved in core aspects of alcoholism, such as the tendency to prefer immediate reward, despite negative consequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51293.RAoUazrixLfnVnLjrEH5z6o4RSBYSP1dUwNE7tyTuVTU4130_provenance.
- NP51299.RAv0bOqNX0VLXI2irHrOitt_hwnD-tqGlsrzCCoPCEKjg130_assertion description "[Family-based and case-control study of DRD2, DAT, 5HTT, COMT genes polymorphisms in alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51299.RAv0bOqNX0VLXI2irHrOitt_hwnD-tqGlsrzCCoPCEKjg130_provenance.
- NP51300.RAhjNMtY3UOjcXvxa0IRbkdZ1CZozv1ke3UKsvlLcmkVw130_assertion description "[Our study was aimed at investigating whether distinct haplotypes, defined by polymorphisms associated with the expressions of DAT and SERT, were associated with subgroups of alcohol dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51300.RAhjNMtY3UOjcXvxa0IRbkdZ1CZozv1ke3UKsvlLcmkVw130_provenance.
- NP51301.RArcy5Nb6vXvlWBQUNyzNyuwTh6sbe28PGOuWKvSe1Sqw130_assertion description "[Serotonin transporter (5-HTTLPR) and monoamine oxidase (MAOA) promoter polymorphisms in women with severe alcoholism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51301.RArcy5Nb6vXvlWBQUNyzNyuwTh6sbe28PGOuWKvSe1Sqw130_provenance.
- NP51303.RAtWJRH95ARoSa1n6Y03ihGgM0DXs_oTzXapTk9la_V5g130_assertion description "[Epistasis between IL1A, IL1B, TNF, HTR2A, 5-HTTLPR and TPH2 variations does not impact alcohol dependence disorder features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51303.RAtWJRH95ARoSa1n6Y03ihGgM0DXs_oTzXapTk9la_V5g130_provenance.
- NP51306.RAheJflKgCR_HOTWzofFmDgrZTSKL36lVjdRwnhCCKQ6k130_assertion description "[This study suggests a putative role of the 5-HTTLPR for alcoholism in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51306.RAheJflKgCR_HOTWzofFmDgrZTSKL36lVjdRwnhCCKQ6k130_provenance.
- NP51314.RAv2q5xBMrllrweuOEpX30g6dc2zm37tm51c75KMS8dG8130_assertion description "[Significance of serotonin transporter gene 5-HTTLPR and variable number of tandem repeat polymorphism in attention deficit hyperactivity disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51314.RAv2q5xBMrllrweuOEpX30g6dc2zm37tm51c75KMS8dG8130_provenance.
- NP51317.RAvwPd5tP4cG1KN4IIHlr5mc6sC3DQtOgBQjBpdqQmygA130_assertion description "[Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51317.RAvwPd5tP4cG1KN4IIHlr5mc6sC3DQtOgBQjBpdqQmygA130_provenance.
- NP51318.RAiHMxDgaoGlrDgvzvLN3m0pCRZaYjUBbU7Bgml2USwuQ130_assertion description "[Association between polymorphisms in serotonin transporter gene and attention deficit hyperactivity disorder in Chinese Han subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51318.RAiHMxDgaoGlrDgvzvLN3m0pCRZaYjUBbU7Bgml2USwuQ130_provenance.
- NP51319.RAm61vKO7rfUCuSph0b46U0AEO3OGYr-ykVIcXNymyHjw130_assertion description "[Therefore, the presence of comorbid psychiatric disorders should be taken into account to clarify the association of the 5-HTTLPR polymorphism with MDD phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51319.RAm61vKO7rfUCuSph0b46U0AEO3OGYr-ykVIcXNymyHjw130_provenance.
- NP51320.RAv7m6FgpUAChq7VflE82y3bb0h1Evs9EHRSaq5gGYGyw130_assertion description "[These results support the hypothesis that GNB3, HTR2A, and SLC6A4 may play a role in the outcome of short-term antidepressant treatment for MDD in an interactive manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51320.RAv7m6FgpUAChq7VflE82y3bb0h1Evs9EHRSaq5gGYGyw130_provenance.
- NP51324.RAlOq1XznHkA_qwdJtKwS1stZNNVQMLqc0mN2mFyfikqM130_assertion description "[The authors examined variations of serotonin transporter-linked promoter region (5-HTTLPR) functional polymorphism in 26 stroke patients with major depression and in 25 unrelated nondepressed stroke subjects of Caucasian descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51324.RAlOq1XznHkA_qwdJtKwS1stZNNVQMLqc0mN2mFyfikqM130_provenance.
- NP51325.RApFGpNzLMo9wrS7NAmo0b8RMaydqzQ9grdP70HrKC7Z8130_assertion description "[Variations in 5-HTTLPR modulate the sensitivity of patients with rMDD and controls to the behavioral effects of TD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51325.RApFGpNzLMo9wrS7NAmo0b8RMaydqzQ9grdP70HrKC7Z8130_provenance.
- NP51328.RAjsJtJwFLS7XaN0x8sZkU8WSZUrq_piilcExpZkjOLDg130_assertion description "[The aim of this work was to explore the possible association between childhood- and early-adolescent-onset DSM-IV depressive disorders (DD; including major depression and dysthymia) and the serotonin transporter-linked promoter polymorphism (5-HTTLPR) locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51328.RAjsJtJwFLS7XaN0x8sZkU8WSZUrq_piilcExpZkjOLDg130_provenance.
- NP51330.RAlzTG36wj6mGo8MSPgvuqDQmE465z6Bw7xMoeEp56S98130_assertion description "[Children's inferential styles, 5-HTTLPR genotype, and maternal expressed emotion-criticism: An integrated model for the intergenerational transmission of depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51330.RAlzTG36wj6mGo8MSPgvuqDQmE465z6Bw7xMoeEp56S98130_provenance.
- NP51336.RAjFa3TejLXnILJlUi6TMBpUmOgRqsx9-OCB0k6-eZfKc130_assertion description "[A polymorphism in the serotonin transporter (5-HTT) gene seems to moderate the influence of stressful life events on depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51336.RAjFa3TejLXnILJlUi6TMBpUmOgRqsx9-OCB0k6-eZfKc130_provenance.
- NP51341.RAg72baSXGDQ1XVltuKxw6WDr-2dycZkKwF8_iQ4zrPIE130_assertion description "[More importantly, future studies need to consider that genetics may be related to behavioral dimensions (compulsivity to impulsivity) instead of to specific psychiatric disorders defined in clinical terms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51341.RAg72baSXGDQ1XVltuKxw6WDr-2dycZkKwF8_iQ4zrPIE130_provenance.
- NP51345.RAsDH_4oeiaxYEoTEVFFvM4Z9uzmLIIBwwwlH3COot45M130_assertion description "[In conclusion, the results (i) suggest an association between serotonergic dysfunction and violent behavior, (ii) provide evidence for an-at least partial-genetic regulation of violent behavior in a subgroup of male offenders, and (iii) suggest a significant role for 5-HT transporter functionality for violent behavior.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51345.RAsDH_4oeiaxYEoTEVFFvM4Z9uzmLIIBwwwlH3COot45M130_provenance.
- NP51347.RAgUVnNy46QWMzY5UkaYaOyp33Pdg80hxG80I3scokhBg130_assertion description "[To test for an association between 5-HTT and BPD, we genotyped three common polymorphisms: the serotonin transporter linked promoter region (5-HTTLPR); a variable number of tandem repeat (VNTR) in intron 2, and a single nucleotide variant (A/G) within the LPR region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51347.RAgUVnNy46QWMzY5UkaYaOyp33Pdg80hxG80I3scokhBg130_provenance.
- NP51351.RAi5niK29FdmT6j6MfhvH5-8J7Ttli0IRh5-qsvaYiH3o130_assertion description "[223 schizophrenia patients were tested with Wisconsin Card Sorting Test (WCST), for the evaluation of cognitive flexibility, Continuous Performance Test (CPT), for the evaluation of attention, and genotyped for the 5-HTTLPR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51351.RAi5niK29FdmT6j6MfhvH5-8J7Ttli0IRh5-qsvaYiH3o130_provenance.
- NP51352.RAmTxr9kpYU0O8W0WyGqTNKmDZxVpaeqKliBu48rY4FUw130_assertion description "[In total 56 patients acutely treated with haloperidol or risperidone either for the first episode of schizophrenia, schizophreniform or schizoaffective disorders, or for the relapse of these psychotic disorders after tapering their maintenance treatment, were genotyped for the 5-HTTLPR L and S alleles and for the new A/G functional variant within the L alelle (La/g).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51352.RAmTxr9kpYU0O8W0WyGqTNKmDZxVpaeqKliBu48rY4FUw130_provenance.
- NP51355.RAk4SKiWTxThpSaGhLYu29PnsQbsN1rtlpN7Rm7R1wMw0130_assertion description "[This study was to aim at investigating the potential interaction for the serotonin receptor gene (5-HTR) 2A and serotonin transporter gene (5-HTTLPR) polymorphisms in the development of schizophrenia, as well as the interaction of the two polymorphisms in relation with symptomatology, family history, age of onset and antipsychotic response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51355.RAk4SKiWTxThpSaGhLYu29PnsQbsN1rtlpN7Rm7R1wMw0130_provenance.
- NP51356.RAgnC4VxRe4JndPQuC0VlFbPZYn6-FBHte7zDd9w7fvl8130_assertion description "[In 260 patients with an ICD-10 diagnosis of schizophrenia (broad definition), we studied the 5-HTTLPR genotype (insertion-deletion polymorphism), the Positive and Negative Syndrome Scale (PANSS), and self-rated inventories (EPI, MMPI, STAI) scores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51356.RAgnC4VxRe4JndPQuC0VlFbPZYn6-FBHte7zDd9w7fvl8130_provenance.
- NP51357.RAsNv4uq718F-SN_zVPDqAwedo5RxwumNP0VE0EnhgGPA130_assertion description "[In contrast with two previous western reports, a recent study on a Chinese population found an association for allele 12 of the variable number tandem repeat (VNTR) in the second intron of the serotonin transporter (5-HTT) gene and schizophrenic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51357.RAsNv4uq718F-SN_zVPDqAwedo5RxwumNP0VE0EnhgGPA130_provenance.
- NP51360.RAvZfOKiJCxaMRFtz2aVIyg6c0RgsOpSZbwDkyFegq7k8130_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." NP51360.RAvZfOKiJCxaMRFtz2aVIyg6c0RgsOpSZbwDkyFegq7k8130_provenance.
- NP51364.RArt2kwwcaP8iZmWRrDXwF8oqhdi0NhYvsTVpKPB4RFWs130_assertion description "[We analyzed five genes, derived from pharmacological or translational mouse models, in a new case-control study of PD and SAD in European Americans: (1) the serotonin transporter (SLC6A4), (2) the serotonin receptor 1A, (3) catechol-O-methyltransferase, (4) a regulator of g-protein signaling and (5) the gastrin-releasing peptide receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51364.RArt2kwwcaP8iZmWRrDXwF8oqhdi0NhYvsTVpKPB4RFWs130_provenance.
- NP51378.RAtpeq2SeFUTZ_GaS0eLuFN-x6FR5xG2UfTObUf1k3mKw130_assertion description "[Polymorphism C in the serotonin transporter gene (SLC6A4) in questionable dementia and Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51378.RAtpeq2SeFUTZ_GaS0eLuFN-x6FR5xG2UfTObUf1k3mKw130_provenance.
- NP51381.RApD1XjQFfs2jSjlzpUITUbEXIdhWxgUQQvwbJJs-C5io130_assertion description "[Association study of polymorphisms in LRP1, tau and 5-HTT genes and Alzheimer's disease in a sample of Colombian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51381.RApD1XjQFfs2jSjlzpUITUbEXIdhWxgUQQvwbJJs-C5io130_provenance.
- NP51386.RArLKSLnpc255CR0-9XlKKYHq-b-a58mbkGFNpQKOIa0Q130_assertion description "[Association between anxiety disorders and a functional polymorphism in the serotonin transporter gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51386.RArLKSLnpc255CR0-9XlKKYHq-b-a58mbkGFNpQKOIa0Q130_provenance.
- NP51387.RAvODw55hQnCvkxdr_wNes_jOAYBxLpACzzpf7H6s7H4Q130_assertion description "[Sib-pair linkage analysis, using the regression method, further supported a role of the 5-HTTLPR in anxiety-related personality traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51387.RAvODw55hQnCvkxdr_wNes_jOAYBxLpACzzpf7H6s7H4Q130_provenance.
- NP51397.RAg0gZIOltwLMaLk9PUBh_ezAVZNdoo-qp-Joh1hDe5ZE130_assertion description "[The present study in a small group of SAD patients was unable to demonstrate that the 5-HTT gene plays a role in the pathogenesis of SAD or in short-term depressive relapse after TRP depletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51397.RAg0gZIOltwLMaLk9PUBh_ezAVZNdoo-qp-Joh1hDe5ZE130_provenance.
- NP51406.RAg3rFk8fiVuMV9VSqgE8O95PvpIxYYLqJxZ2F0O5g6_k130_assertion description "[In this cross-sectional study, we have examined the allelic and genotypic frequencies of a Val-158-Met substitution in the COMT gene, a 44-base pair (bp) length variation in the regulatory region of the serotonin transporter gene (5-HTTLPR) and the T102C and C516T variants in the serotonin receptor type 2A (5HT2A) gene in 79 OCD patients and 202 control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51406.RAg3rFk8fiVuMV9VSqgE8O95PvpIxYYLqJxZ2F0O5g6_k130_provenance.
- NP51410.RAuLZUTW_5V7Hu2xAkEHJMWkmkeCX5YiSyLFlSJ9V_Euo130_assertion description "[However, marginal associations were observed between the 5-HTT LPR and VNTR variants and psychosis (P < or = 0.05) indicating a minor contribution to psychosis of genetic alterations in this gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51410.RAuLZUTW_5V7Hu2xAkEHJMWkmkeCX5YiSyLFlSJ9V_Euo130_provenance.
- NP51411.RAn4Zvr-QW7lMBOBDWij8h1yffs0kiPe7bkIDwCmiedTc130_assertion description "[ we demonstrated that functional deletion/insertion allelic variation associated with decreased expression of serotonin transporter ('s' allele or 'ss' genotype) may restrict expression of schizoid traits in normal subjects and patients with affective disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51411.RAn4Zvr-QW7lMBOBDWij8h1yffs0kiPe7bkIDwCmiedTc130_provenance.
- NP51413.RAvH0vPDbeyRvySEzI-3Y_8ruGJIwuJrpZ-rfyQjq6xu0130_assertion description "[These findings claim for a synergic effect of COMT*H and 5-HTTLPR*S polymorphisms on the risk of psychosis in AD and for their interaction with disease stage and ischemic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51413.RAvH0vPDbeyRvySEzI-3Y_8ruGJIwuJrpZ-rfyQjq6xu0130_provenance.
- NP51415.RAoLPXuuwP_yCbR_jpA5RLF7Ra_A1gzOjfhA5CzyCzTs4130_assertion description "[These results suggest that the investigated polymorphisms were not related to susceptibility to functional psychoses in our Brazilian sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51415.RAoLPXuuwP_yCbR_jpA5RLF7Ra_A1gzOjfhA5CzyCzTs4130_provenance.
- NP51417.RAiOAVCjZjKItkYXFvn1Z0TwR1SjfWNx1rtjBf-8zNNoU130_assertion description "[Novel allelic variants in the human serotonin transporter gene linked polymorphism (5-HTTLPR) among depressed patients with suicide attempt.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51417.RAiOAVCjZjKItkYXFvn1Z0TwR1SjfWNx1rtjBf-8zNNoU130_provenance.
- NP51419.RAqWPFEhh8dCmxBDjab3yUNaIzK6iaaJahl5TJavLA6OA130_assertion description "[Serotonin transporter (5-HTTLPR) genotype, childhood abuse, and suicide attempts in adult psychiatric inpatients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51419.RAqWPFEhh8dCmxBDjab3yUNaIzK6iaaJahl5TJavLA6OA130_provenance.
- NP51420.RAr9lWtC1Z07V0DKfue1uWkqrge1bvXUSat5rwp9F_d5M130_assertion description "[Here, we analyzed the 5-HTTLPR in suicide attempters (n=85).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51420.RAr9lWtC1Z07V0DKfue1uWkqrge1bvXUSat5rwp9F_d5M130_provenance.
- NP51433.RAnWJDvOHZgSCsjlLfc6DGA5Zyn5dmcMrZsabHfw12pog130_assertion description "[We investigated the relationship between COMT Val108/158Met, serotonin transporter coding sequence (5-HT transporter gene-linked polymorphic region; 5-HTTLPR) polymorphisms, and alexithymia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51433.RAnWJDvOHZgSCsjlLfc6DGA5Zyn5dmcMrZsabHfw12pog130_provenance.
- NP51434.RAgt594MmGHkDv4zP4eSpf_l-Ql1s2-eemoMf--GOsUDY130_assertion description "[We investigated both the role of the insertion/deletion polymorphism in the promoter region of the serotonin transporter gene (5-HTTLPR) and that of the Val-158-Met substitution in the catechol-O-methyl-transferase (COMT) gene in conferring susceptibility to TS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51434.RAgt594MmGHkDv4zP4eSpf_l-Ql1s2-eemoMf--GOsUDY130_provenance.
- NP51435.RAozoNd6Cg9AEvQNnXAuQ0QGwNGBX89SQRofIuaoaU8Ck130_assertion description "[As neuroimaging studies allude to dopaminergic and serotonergic dysfunction in GTS and serotonin as an important factor for dopamine release, genotyping of common polymorphisms in the serotonergic receptor (HTR1A: C-1019G; HTR2A: T102C, His452Tyr, A-1438G; HTR2C: C-759T, G-697C) and transporter genes (SLC6A4) was carried out in 87 patients with GTS, compared with 311 matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51435.RAozoNd6Cg9AEvQNnXAuQ0QGwNGBX89SQRofIuaoaU8Ck130_provenance.
- NP51442.RAujz9wPJ_c61AsZl1JKTgyLNUNrvDP2UqG1p90iIy0F0130_assertion description "[The human serotonin transporter gene (5-HTT) is a candidate for the pathogenesis of mood disorders, including bipolar disorder (BPD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51442.RAujz9wPJ_c61AsZl1JKTgyLNUNrvDP2UqG1p90iIy0F0130_provenance.
- NP51445.RAmrubYlD8ZmXMSL36M76BhYcJo6SN0oA7nSiWjl7isNI130_assertion description "[We studied a functional polymorphism of the serotonin transporter (5-HTT) gene (a 44 bp insertion/deletion in the 5-HTT-linked polymorphic region (5-HTTLPR)) and lifetime history of antidepressant-induced mania (AIM) in a population of 305 patients with bipolar affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51445.RAmrubYlD8ZmXMSL36M76BhYcJo6SN0oA7nSiWjl7isNI130_provenance.
- NP51448.RArN7EUPnfdxmVXlEiPoP0XjdTmQDf05mYvsA-fj0Nuak130_assertion description "[Although it will be important to extend the present study in a larger sample, our initial results do not suggest any large association with alleles of the VNTR in the SERT gene and bipolar disorder in Indian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51448.RArN7EUPnfdxmVXlEiPoP0XjdTmQDf05mYvsA-fj0Nuak130_provenance.
- NP51450.RAnaDaPu-0Vp8JXzowv7dOCdUxKAaNMPNstsuzX1ng1jI130_assertion description "[Given the small sample size and the preliminary nature of our findings, replication is necessary.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51450.RAnaDaPu-0Vp8JXzowv7dOCdUxKAaNMPNstsuzX1ng1jI130_provenance.
- NP51453.RAtufWLb7_uc17RwA_zCXNIUSKyaILZtMzNtKJc83b8ys130_assertion description "[Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51453.RAtufWLb7_uc17RwA_zCXNIUSKyaILZtMzNtKJc83b8ys130_provenance.
- NP51462.RAi53C5xEnJxJeJrWbt3VJBqom5eo0QJ5oAMjh5zoPc-A130_assertion description "[Genotypes and allelic frequencies of TPH2, 5-HTTLPR, the 5-HTT (SLC6A4) intron 2 variable-number tandem repeat (VNTR) region, and the MAOA VNTR region were determined in brain-stem samples of 20 `genuine` SIDS cases and compared with results obtained from 150 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51462.RAi53C5xEnJxJeJrWbt3VJBqom5eo0QJ5oAMjh5zoPc-A130_provenance.
- NP51463.RAuY8dM_rl4MwkEaYnw_6S4EXC5P1w-zLThxGrx5UOsUg130_assertion description "[To investigate polymorphisms in the serotonin transporter (5-HTT) gene in cases of sudden infant death syndrome (SIDS) and controls, and further to elucidate a possible relationship between 5-HTT genotypes and external risk factors for SIDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51463.RAuY8dM_rl4MwkEaYnw_6S4EXC5P1w-zLThxGrx5UOsUg130_provenance.
- NP51472.RAm3-Tu58_-IW-GSrOiVAoViEqimQl3mWXhGYc_OjOCDI130_assertion description "[Studies have examined the association between EDs and a functional polymorphism of the serotonin transporter gene promoter (5-HTTLPR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51472.RAm3-Tu58_-IW-GSrOiVAoViEqimQl3mWXhGYc_OjOCDI130_provenance.
- NP51474.RAt6MxPzPCMiuPTNxl0-XW5i1Yu5WE3hxSLgheyLZ48TA130_assertion description "[Manic-depressive illness: an association study with the inositol polyphosphate 1-phosphatase and serotonin transporter genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51474.RAt6MxPzPCMiuPTNxl0-XW5i1Yu5WE3hxSLgheyLZ48TA130_provenance.
- NP51479.RAon0WWezzzXZ8FoyhSOUzNQTtPjVM44bhp_s5MLZzatM130_assertion description "[Therefore, we studied candidate genes in a sample of unrelated patients (n = 102) and healthy controls (n = 79) of Austrian origin, searching for a possible association between polymorphic DNA markers of 5 candidate genes (serotonin transporter, 5-HTT; serotonin 2a receptor, 5-HT2a; dopamine D2 receptor, DRD2; dopamine D3 receptor, DRD3; dopamine transporter, DAT1) and bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51479.RAon0WWezzzXZ8FoyhSOUzNQTtPjVM44bhp_s5MLZzatM130_provenance.
- NP51488.RArX_Swo_NGXKLLXbM7HhJLPoBOcYuPdFKLDF0xbHYn3U130_assertion description "[The human serotonin transporter gene (5-HTT) is a candidate for the pathogenesis of mood disorders, including bipolar disorder (BPD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51488.RArX_Swo_NGXKLLXbM7HhJLPoBOcYuPdFKLDF0xbHYn3U130_provenance.
- NP51495.RAqOHSPjIZ1sOJhpCjx9a3lfXOwOfJjgi4GLUiPl_Sbtc130_assertion description "[Association study of the serotoninergic system in migraine in the Spanish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51495.RAqOHSPjIZ1sOJhpCjx9a3lfXOwOfJjgi4GLUiPl_Sbtc130_provenance.
- NP51496.RAkBLntdZnIeGcFu2Qf2y1OiwOcHWWVLY0K7pr5Q-5RX0130_assertion description "[We report a case-control study with 251 unrelated migraine patients and 192 unrelated healthy controls to evaluate an association between the polymorphisms of the 5-HT transporter (5-HTT) gene rs2066713 and rs1979572 and different migraine phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51496.RAkBLntdZnIeGcFu2Qf2y1OiwOcHWWVLY0K7pr5Q-5RX0130_provenance.
- NP51497.RAgXqq1AxhXaxhyxpmJOIdCYxMkLyhzcSu0FDPRxTCnBg130_assertion description "[The aim of the present observational study was to assess the value of the C825T polymorphism of the beta-3 subunit of G proteins (GNB3) as well as of variants in the SLC6A4 gene (5HTTLPR and STin2 VNTR) and DRD2 gene (TaqI A and NcoI) as predictive markers for consistency in headache response to triptans in migraine patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51497.RAgXqq1AxhXaxhyxpmJOIdCYxMkLyhzcSu0FDPRxTCnBg130_provenance.
- NP51500.RAnOCgcvKO9_Hv_4KnHLVX2z2IrVeQYuG01X30VnneVoE130_assertion description "[This indicates that the 5-HTT may be involved in the polygenic etiology of migraine with aura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51500.RAnOCgcvKO9_Hv_4KnHLVX2z2IrVeQYuG01X30VnneVoE130_provenance.
- NP51502.RAgg0F2Bt1Nmzm3eTGwcY2WfsvX1dXQuX3-GWdkU98l3Q130_assertion description "[To investigate the 5-HTT-gene-linked polymorphic region (5-HTTLPR) genotypes and harm avoidance (HA) dimension in chronic tension-type headache (CTH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51502.RAgg0F2Bt1Nmzm3eTGwcY2WfsvX1dXQuX3-GWdkU98l3Q130_provenance.
- NP51503.RAsbWPu_KGs-drM62mNWycbm_OmDjE2F9XvbOxPjEQjeQ130_assertion description "[Our finding that male IBS-D patients have a reduced frequency of the 5-HTTLPR (ss) genotype contradicts three earlier studies of a similar size, which did not take sex into account.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51503.RAsbWPu_KGs-drM62mNWycbm_OmDjE2F9XvbOxPjEQjeQ130_provenance.
- NP51512.RAmI12Lqb3qFL0pLvNsf0yPWOtrZ-7TM1fDbrV6mN4ShE130_assertion description "[It is conceivable that the presence of the S/S genotype in IBS patients carries an increased risk of the constipation predominant type of IBS, whereas the presence of the 5-HTTLPR allele L/S genotype carries an increased risk of the diarrhea predominant type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51512.RAmI12Lqb3qFL0pLvNsf0yPWOtrZ-7TM1fDbrV6mN4ShE130_provenance.
- NP51515.RAl8KgglD1SAccwOdXYHVqSfXarESeKlA1cFtwqAnF8XU130_assertion description "[Polymorphisms in serotonin-related genes in anorexia nervosa. The first study in Czech population and metaanalyses with previously performed studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51515.RAl8KgglD1SAccwOdXYHVqSfXarESeKlA1cFtwqAnF8XU130_provenance.
- NP51517.RAuS2u1xCsB9LV4tWmJE_VUorx5C8FqWfRuo0F158v3LQ130_assertion description "[Although platelet 5-HTT densities are reduced in patients with cocaine dependence compared with healthy volunteers, these genotypic variations in the serotonin transporter do not seem to influence levels of platelet 5-HTT in cocaine-dependent patients or healthy volunteers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51517.RAuS2u1xCsB9LV4tWmJE_VUorx5C8FqWfRuo0F158v3LQ130_provenance.
- NP51520.RAocuMYBz7ujMbQ1bjvTQ4Inl8ZnU4U_vJIf7SR2dK1Hs130_assertion description "[The possible influence of impulsivity and dietary restraint on associations between serotonin genes and binge eating.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51520.RAocuMYBz7ujMbQ1bjvTQ4Inl8ZnU4U_vJIf7SR2dK1Hs130_provenance.
- NP51523.RAgeg0mSoJ6XzMzI9SZDfygP4D_a3Uo2ioUhqsP2ZLJ_c130_assertion description "[Attenuated concentration of extracellular serotonin due to longer variants may cause higher susceptibility to CFS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51523.RAgeg0mSoJ6XzMzI9SZDfygP4D_a3Uo2ioUhqsP2ZLJ_c130_provenance.
- NP51527.RApW_sXctuupW1UrH7v7ELSHsqypaYyJA7HJtUWX5S6Ho130_assertion description "[A higher frequency of the S/S genotype of 5-HTT was found in FM patients compared with healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51527.RApW_sXctuupW1UrH7v7ELSHsqypaYyJA7HJtUWX5S6Ho130_provenance.
- NP51528.RAsJK5V4SoPxGTvERrTSx23_sXjqqg9P_BzbTFtc7q4hQ130_assertion description "[All controls and FM patients were submitted to genotyping of 5-HTTLPR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51528.RAsJK5V4SoPxGTvERrTSx23_sXjqqg9P_BzbTFtc7q4hQ130_provenance.
- NP51529.RAmuuUaIRY-ZzswxBnRpvhPEmhCtd1dd7j4LoAEJbeF1I130_assertion description "[In conclusion, although comparisons with a heterogeneous control group indicated a possible association between allelic variants of 5-HTTLPR and cocaine dependence among African-American cocaine subjects, this relationship was not observed when the control group was limited to African-American people only. Our findings need to be confirmed on larger samples of ethnically matched individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51529.RAmuuUaIRY-ZzswxBnRpvhPEmhCtd1dd7j4LoAEJbeF1I130_provenance.
- NP51531.RAgcNfegzr4Izx28odJUWIGK4mUW6WryOudE_OvzYldJg130_assertion description "[Because hypoxia and 5-HTT gene polymorphism control 5-HTT expression, we examined 5-HTT gene polymorphism and PH in hypoxemic patients with advanced chronic obstructive pulmonary disease (COPD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51531.RAgcNfegzr4Izx28odJUWIGK4mUW6WryOudE_OvzYldJg130_provenance.
- NP51533.RAt2FB-J0EkUm1MpH5hM7lNwxjf6xFl_WSsM9GN__G7-w130_assertion description "[Genetic contribution to pathological gambling: possible association between a functional DNA polymorphism at the serotonin transporter gene (5-HTT) and affected men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51533.RAt2FB-J0EkUm1MpH5hM7lNwxjf6xFl_WSsM9GN__G7-w130_provenance.
- NP51534.RAsW0QdLCHfJzVN_OBViH7ffO9LOEzEgAcL9v3vq33ZwU130_assertion description "[Our findings confirm reports that the l allele is associated with better SSRI response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51534.RAsW0QdLCHfJzVN_OBViH7ffO9LOEzEgAcL9v3vq33ZwU130_provenance.
- NP51538.RAn08YSxvDZG90F301GiJJESu4z7MBpLVpOH6CsrZiLO4130_assertion description "[Family based association study of DRD1, DRD2, DRD3, DRD4, DAT, COMT gene polymorphism in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51538.RAn08YSxvDZG90F301GiJJESu4z7MBpLVpOH6CsrZiLO4130_provenance.
- NP51539.RArw9DgM4saZrMWMlZm_Ptge-8H5JcAbmJqGvphHCfI6Y130_assertion description "[To fully evaluate SLC6A3 as a therapeutic antipshycotic target we investigated association of the gene with responses to chlorpromazine and clozapine and with chlorpromazine-induced extrapyramidal syndrome (EPS) in the Chinese schizophrenia population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51539.RArw9DgM4saZrMWMlZm_Ptge-8H5JcAbmJqGvphHCfI6Y130_provenance.
- NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_assertion description "[Our objectives were (i) to examine epistasis between the DAT 3' UTR variable number of tandem repeats (VNTR) and COMT Val158Met polymorphisms on brain activation during executive function, and (ii) to then determine the extent to which such interaction is altered in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51540.RAilv3Zd05d45Sz7OIqBp-J0fbi7i4BvaeXMCwU370pFo130_provenance.
- NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_assertion description "[Inherited or acquired dysfunction of the dopamine system is believed to underlie the core symptoms of schizophrenia, and there are some evidences that dopamine transporter activity may be altered in schizophrenic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51544.RAlgi2XtpNcT5VZovMyPV9ByXIWo0ZLWqFSihUZ0GFsaw130_provenance.
- NP51547.RAvaZ4n1ZYqrwfJ6ilsniZMBie38KUMaZ7HHY7PSeIEgs130_assertion description "[In this study, we used a family-based association approach to investigate the implication of dopamine-related candidate genes, which had been previously reported as possibly associated with TS genes that encode for the dopamine receptors DRD2, DRD3 and DRD4, the dopamine transporter 1 (SLC6A3) and the monoamine oxidase-A (MAO-A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51547.RAvaZ4n1ZYqrwfJ6ilsniZMBie38KUMaZ7HHY7PSeIEgs130_provenance.
- NP51549.RAqVfG5tHW18__J5Bqkt8RsuTQqrsBtc0oU2z72L8xzIM130_assertion description "[In summary, allele frequencies did not differ between cases and controls, but DAT1 genotype accounted for variations of tic severity within the TS group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51549.RAqVfG5tHW18__J5Bqkt8RsuTQqrsBtc0oU2z72L8xzIM130_provenance.
- NP51552.RAj1m5O8TzoynabMLb-P0Td0p-DIHxy5rGzS7ybPcUfgc130_assertion description "[Significant association was observed for monoamine oxidase-B(MAO-B) variant allele G and PD, whereas no difference in genotype and allele frequencies was observed for manganese-superoxide dismutase (MnSOD), dopamine receptor-D2(DRD2), and dopamine transporter (DAT) genes between controls and PD cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51552.RAj1m5O8TzoynabMLb-P0Td0p-DIHxy5rGzS7ybPcUfgc130_provenance.
- NP51553.RAj4tntaHShHWu6R1S2wiJewJDj7-0naJNqUtesdc40H8130_assertion description "[Dopamine transporter gene polymorphism, spect imaging, and levodopa response in patients with Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51553.RAj4tntaHShHWu6R1S2wiJewJDj7-0naJNqUtesdc40H8130_provenance.
- NP51555.RAnYVoPU49Al3rNVNqn-CnqoYj19JLblxtgC7voOIzAxw130_assertion description "[Smoking, genes encoding dopamine pathway and risk for Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51555.RAnYVoPU49Al3rNVNqn-CnqoYj19JLblxtgC7voOIzAxw130_provenance.
- NP51557.RApJKFKC9wuoY_gDj4yGcjGLpB5RdXx-AGX2sjP23MVSU130_assertion description "[Many small studies have reported associations between genetic polymorphisms and PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51557.RApJKFKC9wuoY_gDj4yGcjGLpB5RdXx-AGX2sjP23MVSU130_provenance.
- NP51558.RAlUhzdKkz5uPzX0qLz39rv3pIrgp_-Gt_vJydnMCwKS0130_assertion description "[Further replication and functional studies are now required to fully understand the consequence of polymorphisms present at both the 5' and 3' ends of the DAT1 gene and their role in ADHD pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51558.RAlUhzdKkz5uPzX0qLz39rv3pIrgp_-Gt_vJydnMCwKS0130_provenance.
- NP51559.RAoPIu1A_hh__oLKYUQZFZc_UsFV1nveXVYBcl7gU-8y8130_assertion description "[These findings provide initial evidence that environmental risks as described by the Rutter Family Adversity Index moderate the impact of the DAT1 gene on ADHD symptoms, suggesting a DAT1 effect only in those individuals exposed to psychosocial adversity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51559.RAoPIu1A_hh__oLKYUQZFZc_UsFV1nveXVYBcl7gU-8y8130_provenance.
- NP51561.RArmieZIgL1LcsiV3vxRMbbrr5hZnUuhwySeAoiVrQLcA130_assertion description "[Dopamine transporter genotype influences the physiological response to medication in ADHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51561.RArmieZIgL1LcsiV3vxRMbbrr5hZnUuhwySeAoiVrQLcA130_provenance.
- NP51566.RAkOtr1kjqa-B6r_8TGja4RHMXZA4ZOaEaKeI3wvebRqw130_assertion description "[According to a meta-analysis, the DAT1 gene, an obvious candidate gene in ADHD vulnerability, does not appear to be involved (OR = 1.13, p = 0.21).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51566.RAkOtr1kjqa-B6r_8TGja4RHMXZA4ZOaEaKeI3wvebRqw130_provenance.
- NP51569.RAvhpgbrhNDyRDy6ptEjRnVq1GClyrUiys4_eK53E7CCU130_assertion description "[Our findings provide further evidence that the 3'UTR of the DAT1 gene affects vulnerability to severe alcohol withdrawal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51569.RAvhpgbrhNDyRDy6ptEjRnVq1GClyrUiys4_eK53E7CCU130_provenance.
- NP51574.RAiz0XPVea3-rG2rBt9GdhWf_ndgBfvDbS5yeHiK-m3pI130_assertion description "[Genetic polymorphisms of the promoter region of dopamine D2 receptor and dopamine transporter genes and alcoholism among four aboriginal groups and Han Chinese in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51574.RAiz0XPVea3-rG2rBt9GdhWf_ndgBfvDbS5yeHiK-m3pI130_provenance.
- NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc130_assertion description "[For the first time, these findings provide tentative evidence of the contribution of the DAT1 gene core promoter polymorphism to the etiopathophysiology of bipolar disorder at least in the Iranian population that we have studied. Interestingly, no allelic or genotype association was observed in the female patients (P]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc130_provenance.