Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP57208.RAvWysT7pwL0B_P6f_V4wSmF8G_MYukMxECG05S_vGuF4130_assertion description "[Our result suggested that 5-HT(2A) receptor gene polymorphism (A-1438G) appears to be associated with self-determinism and self-transcendence (ST). Our result also indicated a significant relationship between 5-HT(6) receptor gene polymorphism (C267T) and ST. Further studies of polymorphisms of other genes and their interactions may clarify the complex relationship between personality and genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57208.RAvWysT7pwL0B_P6f_V4wSmF8G_MYukMxECG05S_vGuF4130_provenance.
- NP57211.RApgiu7BMlUyTiTm1lcWHBy3fFcEgg7D_nfFBf3YppPLE130_assertion description "[Association study of the 5-HT6 receptor gene in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57211.RApgiu7BMlUyTiTm1lcWHBy3fFcEgg7D_nfFBf3YppPLE130_provenance.
- NP57212.RAoZpFUVXf01_okuFoOt1NVJfYoWp5I4qMZXMf9DYSrlc130_assertion description "[We conducted a pharmacogenetic study to evaluate whether variants in dopamine-related genes (DRD1-DRD5, AKT1 and GSK3beta) and serotonin receptor genes (HTR1A, HTR1B, HTR1D, HTR2A, HTR2C, HTR6 and HTR7) can be used to predict the efficacy of risperidone treatment for schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57212.RAoZpFUVXf01_okuFoOt1NVJfYoWp5I4qMZXMf9DYSrlc130_provenance.
- NP57213.RAlK9W5pF5c4yCtfEe0H93HNuoNPzeKFceyUuHcxoJLsg130_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." NP57213.RAlK9W5pF5c4yCtfEe0H93HNuoNPzeKFceyUuHcxoJLsg130_provenance.
- NP57214.RApbOzC8dXBE6nHqYm5J1ZIA1CULq2uFlAjLFcLh-uwyk130_assertion description "[Multiple genetic factors in olanzapine-induced weight gain in schizophrenia patients: a cohort study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57214.RApbOzC8dXBE6nHqYm5J1ZIA1CULq2uFlAjLFcLh-uwyk130_provenance.
- NP57217.RAlCckjwnxFohoOHQr8dYN_RK6Bkt942zxoyAdr31ZwhM130_assertion description "[Association analysis of the 5-HT6 receptor polymorphism C267T with depression in patients with Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57217.RAlCckjwnxFohoOHQr8dYN_RK6Bkt942zxoyAdr31ZwhM130_provenance.
- NP57218.RAkcxE-gmzWij8SdwuuH8b6ZO7Djn3Q0sOkT_uNo4AJBQ130_assertion description "[Association analysis of the 5-HT6 receptor polymorphism C267T in Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57218.RAkcxE-gmzWij8SdwuuH8b6ZO7Djn3Q0sOkT_uNo4AJBQ130_provenance.
- NP57219.RAgcg5jsQwT-alrr2hz1RRJgyrcWFUD1CdSiyiRrIYDLI130_assertion description "[Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57219.RAgcg5jsQwT-alrr2hz1RRJgyrcWFUD1CdSiyiRrIYDLI130_provenance.
- NP57221.RArhna25S7kIK0h8ld7PJePP1HP6KL6LalklV6nLaTna8130_assertion description "[We investigated the association between the C267T polymorphism of the 5-HT6 gene and PD and found that individuals carrying the T allele had significatnly lower risk for developing PD]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57221.RArhna25S7kIK0h8ld7PJePP1HP6KL6LalklV6nLaTna8130_provenance.
- NP57226.RAnlFtKmrFnsscuO1OSjQS8xqz47qhzJJyVyWEoGWRrg0130_assertion description "[These findings suggest that haplotype A-T itself may inhibit the occurrence of schizophrenia, or that another susceptible genetic variants may exist within linkage disequilibrium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57226.RAnlFtKmrFnsscuO1OSjQS8xqz47qhzJJyVyWEoGWRrg0130_provenance.
- NP57230.RAphgl1P-7Tx0n692-kf_WHGGMSrHrCE9q12xV6oO41ss130_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." NP57230.RAphgl1P-7Tx0n692-kf_WHGGMSrHrCE9q12xV6oO41ss130_provenance.
- NP57231.RAi5O7_P5xTwlPbKUiHYIiktHwDI1N8JNoMLmuE6P86OU130_assertion description "[ The present results suggest that the HTR3A and DBH genes may participate in the regulation of dopamine and serotonin turnover rates in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57231.RAi5O7_P5xTwlPbKUiHYIiktHwDI1N8JNoMLmuE6P86OU130_provenance.
- NP57233.RAmzWljsPpIiTV6ecGyEuBTaTK6B0FKA8OYcKcOIrLvu8130_assertion description "[These findings show that the C178T(Pro16Ser) variant in HTR3A may represent a functional variant and affect the susceptibility to bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57233.RAmzWljsPpIiTV6ecGyEuBTaTK6B0FKA8OYcKcOIrLvu8130_provenance.
- NP57234.RAvCDsHb951io5Bm3NrwmWqtrGfK0DdqGbgVQhZDZ5JD8130_assertion description "[These findings show that the C178T(Pro16Ser) variant in HTR3A may represent a functional variant and affect the susceptibility to bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57234.RAvCDsHb951io5Bm3NrwmWqtrGfK0DdqGbgVQhZDZ5JD8130_provenance.
- NP57237.RAqjj5eJ1V8gHH3dCHWtJwI4ppymGVi5sELsq42xmSzRA130_assertion description "[These findings show that the C178T(Pro16Ser) variant in HTR3A may represent a functional variant and affect the susceptibility to bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57237.RAqjj5eJ1V8gHH3dCHWtJwI4ppymGVi5sELsq42xmSzRA130_provenance.
- NP57240.RAv4VqXemfuCBJv7pnfyMtVDKdiN5Jbzw2dH2ppi-AXmg130_assertion description "[These findings show that the C178T(Pro16Ser) variant in HTR3A may represent a functional variant and affect the susceptibility to bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57240.RAv4VqXemfuCBJv7pnfyMtVDKdiN5Jbzw2dH2ppi-AXmg130_provenance.
- NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_assertion description "[Although these data should be interpreted cautiously due to the small sample size, these results implicate TPH1 and SLC6A4 in general response, and HTR2A, TPH2, and MAOA in the specificity of response to fluoxetine. Intriguingly, we observe that a number of the less frequent alleles of many of the SNP markers were associated with the nonresponse and nonspecific phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_provenance.
- NP57247.RAoIBtrp8bq-Bn5_wVwjqxdY60ZGnGgpWxAb8SZBKtRWc130_assertion description "[Assuming that genes regulating the serotonin system are involved in the pathogenesis of panic disorder, the authors searched for a genetic association of panic disorder with the serotonin 1A (HTR1A), 2A (HTR2A), and 2C (HTR2C) receptor genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57247.RAoIBtrp8bq-Bn5_wVwjqxdY60ZGnGgpWxAb8SZBKtRWc130_provenance.
- NP57255.RAvnOzdsKJImxezdnptcB_qcba0IJumdPBIWc20KStpMc130_assertion description "[An association was observed between polymorphisms in HTR2A and HTR2C genes and occurrence of acute EPS in schizophrenic patients treated with perphenazine monotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57255.RAvnOzdsKJImxezdnptcB_qcba0IJumdPBIWc20KStpMc130_provenance.
- NP57259.RAvSo8no-p7fkYvhtwqDJIjvQcnNhLxUUWuR-vG6bZDkc130_assertion description "[The association between HTR2C gene polymorphisms and the metabolic syndrome in patients with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57259.RAvSo8no-p7fkYvhtwqDJIjvQcnNhLxUUWuR-vG6bZDkc130_provenance.
- NP57267.RAgiBByxFzmdlPJGCeP5NLEVFa1-XYcmP-f_IH2bQNmxo130_assertion description "[Further evidence supporting the association between 5HTR2C gene and bipolar disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57267.RAgiBByxFzmdlPJGCeP5NLEVFa1-XYcmP-f_IH2bQNmxo130_provenance.
- NP57271.RAplYyCfopiZz-Hv-3cF4JtTNea6UPPWPecPWUlPC2Hmk130_assertion description "[A haplotype analyses between the (GT)12-18/(CT)4-5 motif and a Cys23Ser variant of the 5-HT2C gene (which had previously been genotyped in the same sample) showed similar distributions between cases and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57271.RAplYyCfopiZz-Hv-3cF4JtTNea6UPPWPecPWUlPC2Hmk130_provenance.
- NP57272.RAjy7u6Q9czR5yPWCOR-KXvQvn95_Pf2LDYsbITUFsFuI130_assertion description "[A haplotype analyses between the (GT)12-18/(CT)4-5 motif and a Cys23Ser variant of the 5-HT2C gene (which had previously been genotyped in the same sample) showed similar distributions between cases and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57272.RAjy7u6Q9czR5yPWCOR-KXvQvn95_Pf2LDYsbITUFsFuI130_provenance.
- NP57273.RArtTRws4s-ex2D18uJqK8XBjXFUuuisi8tgsu6SW9QgM130_assertion description "[A haplotype analyses between the (GT)12-18/(CT)4-5 motif and a Cys23Ser variant of the 5-HT2C gene (which had previously been genotyped in the same sample) showed similar distributions between cases and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57273.RArtTRws4s-ex2D18uJqK8XBjXFUuuisi8tgsu6SW9QgM130_provenance.
- NP57279.RAi0aURp__N8TZPlmKv5ZaGHc1raP6NRzli7lKokbq1zQ130_assertion description "[Evaluation of a Cys23Ser mutation within the human 5-HT2C receptor gene: no evidence for an association of the mutant allele with obesity or underweight in children, adolescents and young adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57279.RAi0aURp__N8TZPlmKv5ZaGHc1raP6NRzli7lKokbq1zQ130_provenance.
- NP57281.RAso5SskHfV0orZzUrAiyvFEqx_lnxj3ZXT5Ek21z3YUg130_assertion description "[Our findings suggest that common HTR2C gene variants are unlikely to have a major role in obesity- and mental health-related traits in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57281.RAso5SskHfV0orZzUrAiyvFEqx_lnxj3ZXT5Ek21z3YUg130_provenance.
- NP57282.RAoBL-frXCnOIodweSskZgD0geOCQpcsUYjiFiVYM9NRg130_assertion description "[Combined HTR2C-LEP genotype as a determinant of obesity in patients using antipsychotic medication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57282.RAoBL-frXCnOIodweSskZgD0geOCQpcsUYjiFiVYM9NRg130_provenance.
- NP57286.RAqGbB4ohqHTtGfHSSEgFYIBW6KBW60NkT9R3yxBE7WGg130_assertion description "[Candidate genes for alcohol dependence: a review of genetic evidence from human studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57286.RAqGbB4ohqHTtGfHSSEgFYIBW6KBW60NkT9R3yxBE7WGg130_provenance.
- NP57291.RAhEfp9eIHkRnpaxrqhEpiJbac7EnnbEjMycwvTYCJJrY130_assertion description "[The 102-T/C polymorphism of the 5-HT(2A) receptor gene was analysed in 159 patients with major depression and 164 unrelated and healthy controls using a case-control design.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57291.RAhEfp9eIHkRnpaxrqhEpiJbac7EnnbEjMycwvTYCJJrY130_provenance.
- NP57292.RAqN5B9Wdx3rG8warJ6d1m7gmIPnjJv3ciDRV6yc4Y1jE130_assertion description "[we suggest that HTR2A may play an important role in the pathophysiology of the therapeutic response to SSRIs in Japanese MDD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57292.RAqN5B9Wdx3rG8warJ6d1m7gmIPnjJv3ciDRV6yc4Y1jE130_provenance.
- NP57296.RAiSBIGlpue9S8dvWyYPMNhcV0pODTFxzrsnhG2fiLXpM130_assertion description "[Response to fluoxetine and serotonin 1A receptor (C-1019G) polymorphism in Taiwan Chinese major depressive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57296.RAiSBIGlpue9S8dvWyYPMNhcV0pODTFxzrsnhG2fiLXpM130_provenance.
- NP57301.RAjQf9s6Jp7POFUKkn2nmtsOtHxiJky8QUVFS2fnIM5XA130_assertion description "[This study aimed to investigate the possible association between T102C and -1438 G/A polymorphism in the 5-HT2A receptor gene and susceptibility to and clinical features of obsessive-compulsive disorder (OCD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57301.RAjQf9s6Jp7POFUKkn2nmtsOtHxiJky8QUVFS2fnIM5XA130_provenance.
- NP57302.RAqoCyQOiDzAOTqpFLF2M_xOqxCeEVHyHfKovAEL6zliE130_assertion description "[In this, to our knowledge, first association study based on children and adolescents with OCD, we confirm an association of the A-allele of the 5-HT2A receptor gene with OCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57302.RAqoCyQOiDzAOTqpFLF2M_xOqxCeEVHyHfKovAEL6zliE130_provenance.
- NP57313.RAvfObeVFGj9UYeKCgq4RRZYOvh-_43ajYfhN1bPL1I7U130_assertion description "[Investigation of association of the brain-derived neurotrophic factor (BDNF) and a serotonin receptor 2A (5-HTR2A) genes with voluntary and involuntary attention in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57313.RAvfObeVFGj9UYeKCgq4RRZYOvh-_43ajYfhN1bPL1I7U130_provenance.
- NP57314.RAqgPFqq2mxueriZPz_1O7pPLw-1ip9xmTPC9NPazXXYo130_assertion description "[Association between T102C and A-1438G polymorphisms in the serotonin receptor 2A (5-HT2A) gene and schizophrenia: relevance for treatment with antipsychotic drugs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57314.RAqgPFqq2mxueriZPz_1O7pPLw-1ip9xmTPC9NPazXXYo130_provenance.
- NP57316.RAocVYXLWTqBEBlT6NfGr64wKIHPfQptMTU3HvdefiTbI130_assertion description "[Haplotype analysis supported an association of the cholecystokinin gene TG haplotype with the PD-all group (P = 0.04), whereas DRD1 receptor CAA and HTR2A receptor AT haplotypes were associated with a lower risk for PD-pure phenotype (P = 0.03 and P = 0.04, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57316.RAocVYXLWTqBEBlT6NfGr64wKIHPfQptMTU3HvdefiTbI130_provenance.
- NP57320.RAppDaaadIJw_zcDW3buOX6obHL2Tofh2VIH8DKqOCuSE130_assertion description "[It is suggested that increase of IMT and formation of plaque are risk factors in patients aged 50 or above with hypertension, and that careful observation of the carotid artery will be effective for early detection of arteriosclerosis, and to predict the symptoms thereof.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57320.RAppDaaadIJw_zcDW3buOX6obHL2Tofh2VIH8DKqOCuSE130_provenance.
- NP57322.RApb7WjVLNobcEVP_Joqo9lejuvVvX-pIi5FcFlER756A130_assertion description "[ This data indicates that the T102C polymorphism in the 5-HT(2A) gene might be an independent risk factor for increased blood pressure in female individuals with essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57322.RApb7WjVLNobcEVP_Joqo9lejuvVvX-pIi5FcFlER756A130_provenance.
- NP57328.RAvUQtSV4-j0Y6uEcGjZaDBcyzPWPUlO6QA86fEihC6ck130_assertion description "[However, there were significant associations between HTR2A and personality traits in the BPD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57328.RAvUQtSV4-j0Y6uEcGjZaDBcyzPWPUlO6QA86fEihC6ck130_provenance.
- NP57331.RAhVMjqqMXhFePq32z45Idb__s-sMbqrJ4c780y_k1rV0130_assertion description "[Using PCR-RFLP analysis, we have conducted a study of polymorphic loci of several genes of this system: C1019G of serotonin receptor 1A gene, (HTR1A); A438G of serotonin receptor 2A gene, (HTR2A); G861C of serotonin receptor 1B gene, (HTR1B); Stin2VNTR and 5-HTTLPR of serotonin transporter gene (SLC6A4) in patients with unipolar depression among ethnic Tatars and Russians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57331.RAhVMjqqMXhFePq32z45Idb__s-sMbqrJ4c780y_k1rV0130_provenance.
- NP57333.RAq9GoaeRTZYx-yIjqn8g_TMkbHJHx2HkSkVO2bj1n-1E130_assertion description "[Polymorphisms in the genes encoding the serotonin transporter and the brain derived neurotrophic factor interact with recent stressful life events on depression among patients with no history of previous depressive episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57333.RAq9GoaeRTZYx-yIjqn8g_TMkbHJHx2HkSkVO2bj1n-1E130_provenance.
- NP57334.RAif5UpxzQTzRcsHgi9PkDXJDM6nRWBkPGp_QuSXGlbAg130_assertion description "[TPH2 -703G/T SNP may have important effect on susceptibility to suicidal behavior in major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57334.RAif5UpxzQTzRcsHgi9PkDXJDM6nRWBkPGp_QuSXGlbAg130_provenance.
- NP57335.RAjnsuNfL9xOx51B-RDkSP8Fnel_sRA90SyIvwxgNXfCc130_assertion description "[We concluded that these polymorphisms may not be associated with susceptibility to suicidal behavior in our Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57335.RAjnsuNfL9xOx51B-RDkSP8Fnel_sRA90SyIvwxgNXfCc130_provenance.
- NP57336.RArbaiW8Yl8Tr_SXtRBHJL0rsNXjYR3hqLj6QgtOLgQJg130_assertion description "[These data indicate that the genes in the serotonergic pathway may be involved in the development of type II alcoholism but the gene effects are very small.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57336.RArbaiW8Yl8Tr_SXtRBHJL0rsNXjYR3hqLj6QgtOLgQJg130_provenance.
- NP57341.RAsw8mEjmre36iKkGFrU6Nvtbr-pW2aH9Kb10SlrOmkpE130_assertion description "[Family history of alcoholism is associated with lower 5-HT2A receptor binding in the prefrontal cortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57341.RAsw8mEjmre36iKkGFrU6Nvtbr-pW2aH9Kb10SlrOmkpE130_provenance.
- NP57345.RAnRsuGM00_30xe2e67DAyFi5vtQ_BNoh5jjpxmu4TBec130_assertion description "[These results suggested that liability to suicide behavior might be associated with A-1438G polymorpyhism of 5-HT2A receptor gene in male subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57345.RAnRsuGM00_30xe2e67DAyFi5vtQ_BNoh5jjpxmu4TBec130_provenance.
- NP57347.RAj7_IuQdreenYde4AmvGbNiSwdM1EsWiCLnY6Ve8yS18130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57347.RAj7_IuQdreenYde4AmvGbNiSwdM1EsWiCLnY6Ve8yS18130_provenance.
- NP57352.RAtm4r1-7KVOAKq4XfkiBZVHSkYJemLGQMXy6EB-097Ug130_assertion description "[In order to identify gene variants related to the serotonergic neurotransmitter system that possibly represent a hereditary risk factor for sporadic Alzheimer's disease (AD), patients suffering from AD and non-demented psychiatric inpatients without symptoms of dementia were genotyped for polymorphisms of HTR6 (267C/T) and HTR2A (-1438G/A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57352.RAtm4r1-7KVOAKq4XfkiBZVHSkYJemLGQMXy6EB-097Ug130_provenance.
- NP57353.RAhvCqnIKsdHUmoqzLWwGREXGp1RBd498dL_17uOof6vw130_assertion description "[ Specific NP symptoms in AD were significantly associated with 5-HT(2A) receptor polymorphisms. Possible ethnic differences in the behavioral expression of 5-HT(2A) receptor polymorphisms are worthy of further exploration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57353.RAhvCqnIKsdHUmoqzLWwGREXGp1RBd498dL_17uOof6vw130_provenance.
- NP57354.RAiGDEA2RMzd9lWQjwazUde_dZ-otJ_OFUzpDYVsIDEdM130_assertion description "[ Our data strongly confirm and extend to FAD previous studies suggesting that the genetic variation at this locus is associated with prominent psychotic features in AD and that the 102C allele could play an important role in late-onset AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57354.RAiGDEA2RMzd9lWQjwazUde_dZ-otJ_OFUzpDYVsIDEdM130_provenance.
- NP57356.RAohOf5m_Ib77Lh0SEQkTFWxVlXQa1JEOIDCPmTa4Klu4130_assertion description "[Analysis of the 5HT-2A T102C receptor polymorphism and psychotic symptoms in Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57356.RAohOf5m_Ib77Lh0SEQkTFWxVlXQa1JEOIDCPmTa4Klu4130_provenance.
- NP57366.RAr0ZI41d6Ww7e1m9FR0Up4xx7hObIG7pEUIuFnQsAezk130_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." NP57366.RAr0ZI41d6Ww7e1m9FR0Up4xx7hObIG7pEUIuFnQsAezk130_provenance.
- NP57373.RAmcROU9NWhoCp-KGuoIf7WtMqQQT8mLjBcFEsq_LSK1Y130_assertion description "[Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57373.RAmcROU9NWhoCp-KGuoIf7WtMqQQT8mLjBcFEsq_LSK1Y130_provenance.
- NP57377.RAsbZLY3bVOj5vtZsSI25IJjnlVRzeBJLRQ17sXKIW4Tk130_assertion description "[Pharmacogenetics of risperidone therapy in autism: association analysis of eight candidate genes with drug efficacy and adverse drug reactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57377.RAsbZLY3bVOj5vtZsSI25IJjnlVRzeBJLRQ17sXKIW4Tk130_provenance.
- NP57381.RAvq1BxiY0BixYgsxq6i_-MaB63kdISd2wa44a74HdgEg130_assertion description "[However, the present study suggests the possibility that an abnormal production rate of the 5-HT(2A)R c.1438A>G gene product might lead to the development of abdominal obesity in men but not in women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57381.RAvq1BxiY0BixYgsxq6i_-MaB63kdISd2wa44a74HdgEg130_provenance.
- NP57383.RApCHRJUrrDt-fyorRzF6BQX_eqYxpZTtZI-scM5bWJnA130_assertion description "[ The T102C polymorphism of the 5-HT2A receptor gene is not directly related to the increased risk of migraine. The associations between the genotypes of this gene and aura may suggest that 5-HT2A receptor gene polymorphism may be involved in determining the subtypes of or accompanying symptoms in the migraine disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57383.RApCHRJUrrDt-fyorRzF6BQX_eqYxpZTtZI-scM5bWJnA130_provenance.
- NP57390.RAinSiMaaC4Y-yxXMDD3gZhfcXqFh9n1BflpP-oN1UmBQ130_assertion description "[In conclusion, this study demonstrates that alcoholism is heterogeneous and male alcohol abuse with behavioral problems was associated with T/C 102 polymorphism of the 5HT2A receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57390.RAinSiMaaC4Y-yxXMDD3gZhfcXqFh9n1BflpP-oN1UmBQ130_provenance.
- NP57396.RAoBq9kojUsvoc-vKiRMlPkYdOK53M2f5eSsgtGwGcrso130_assertion description "[Potential relevant OCD phenotypes founded on age of onset, positive family history for OCD, clinical subtypes, comorbidity and symptom severity were stratified according to 5-HTT, 5-HT1B and 5-HT2A genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57396.RAoBq9kojUsvoc-vKiRMlPkYdOK53M2f5eSsgtGwGcrso130_provenance.
- NP57402.RAvuQkJnKfnetq7cwTLyRcJrmRjHbDtyturrx4stQI7Mo130_assertion description "[Several studies have suggested that the serotonin receptor 1B gene (5HT1B) may be important in the pathogenesis of alcohol dependence (alcoholism; ALC; AD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57402.RAvuQkJnKfnetq7cwTLyRcJrmRjHbDtyturrx4stQI7Mo130_provenance.
- NP57406.RAssNzRubIbrb1xo-FjQnuaV7qe71ZqIqeuox6AnSuwRI130_assertion description "[Substance abuse disorder and major depression appear to be associated with the h5-HTR(1B) G861C locus in the patient population, but other psychopathologies such as bipolar disorder, schizophrenia, alcoholism, and suicide attempts were not found to be associated with this polymorphism. This preliminary result will need replication, given the limitations of association studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57406.RAssNzRubIbrb1xo-FjQnuaV7qe71ZqIqeuox6AnSuwRI130_provenance.
- NP57409.RAkoAUuenFUEcgdHVihKswzoz6xRwUrpfnq-_mdwJqM5k130_assertion description "[These results suggest that 5-HTR1A C (-1019) G polymorphism is probably associated with MDD and it is likely to be the susceptible gene locus for the female and late-onset MDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57409.RAkoAUuenFUEcgdHVihKswzoz6xRwUrpfnq-_mdwJqM5k130_provenance.
- NP57416.RAsXPWPKzZCKwoRDJCdQTbz0Tx63Bf1w1G3Fs2EQCMy00130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57416.RAsXPWPKzZCKwoRDJCdQTbz0Tx63Bf1w1G3Fs2EQCMy00130_provenance.
- NP57418.RAiFayX9nRmTt-nPThxCtk7ayrGU7deF3Z3y3HMvZklO4130_assertion description "[Serotonin receptor HTR1A and HTR2C variants and personality traits in suicide attempters and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57418.RAiFayX9nRmTt-nPThxCtk7ayrGU7deF3Z3y3HMvZklO4130_provenance.
- NP57435.RAsOh3KF7k14RkfcV6JV-iskqfRoE7FZT_7JIMOYUKKec130_assertion description "[We attempt to show that the interaction between 5-HT1A and BDNF polymorphism predicts the risk of treatment-resistant depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57435.RAsOh3KF7k14RkfcV6JV-iskqfRoE7FZT_7JIMOYUKKec130_provenance.
- NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_assertion description "[While the study has several limitations, the results are consistent with a growing body of literature that suggests that the pharmacogenetics of depression (an inherently complex disorder) may turn out to be multifactorial, and may include the HTR1A gene in concert with other serotonin-related genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57437.RAqLrR8q2pipbji66SlXlLlyRGIMxlAmTSurNMdf3X2Q0130_provenance.
- NP57439.RAgP_bl2h4EX_4o0RZQzxT3nHXjNRoJMILpY3taWINmRA130_assertion description "[Is the cPLA2 gene associated with schizophrenia?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57439.RAgP_bl2h4EX_4o0RZQzxT3nHXjNRoJMILpY3taWINmRA130_provenance.
- NP57445.RAkjhyTglxPflsFZwbPdm9vaDXuX4-V1Vl8bd7SfbWelY130_assertion description "[The C379T mutation in Hsp27 also causes CMT disease type 2, except for distal hereditary motor neuropathy, and the phenotypes are distinct from the family with CMT disease type 2F described previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57445.RAkjhyTglxPflsFZwbPdm9vaDXuX4-V1Vl8bd7SfbWelY130_provenance.
- NP57448.RAnfX0SA6ghwn2KgWukAvKZ-0BSgwJ1EywXeCFrAEPR-c130_assertion description "[To the best of our knowledge, this is the first report on the association between a polymorphism of a gene coding for the chaperone protein and lung cancer risk. Moreover, the simple method reported here, based on the dual-luciferase reporter assay system, can be useful for testing functional significance of polymorphisms located in introns of other genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57448.RAnfX0SA6ghwn2KgWukAvKZ-0BSgwJ1EywXeCFrAEPR-c130_provenance.
- NP57450.RAuiopVL7iFEe04sK3MjBAoWZp-inQepDhfXYb42ohQ7w130_assertion description "[ Genetic variations in the IL-6 and IL-1ra gene identify IBD patients at risk for increased bone loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57450.RAuiopVL7iFEe04sK3MjBAoWZp-inQepDhfXYb42ohQ7w130_provenance.
- NP57454.RAsEymYTWiQxSwyuXlH5brzy4SRlaxdCK1PIyAtIb1nlM130_assertion description "[Caucasian patients carrying the HSP70-2 PstI-polymorphism seem to have a more severe form of Crohn's disease (perforations, abscesses, fistulas, conglomerate tumors).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57454.RAsEymYTWiQxSwyuXlH5brzy4SRlaxdCK1PIyAtIb1nlM130_provenance.
- NP57456.RAu9czihtrWMVmYiuDu31kJSXfxbqsnqhi2CKjo74o3tE130_assertion description "[Results found by TDT-STDT have confirmed the involvement of the TNF -308 gene polymorphism in AITD pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57456.RAu9czihtrWMVmYiuDu31kJSXfxbqsnqhi2CKjo74o3tE130_provenance.
- NP57461.RAvq6mNgAGq8J3tYV8tfH_58cGb9-G5Ro37RituwTq8Nw130_assertion description "[ We concluded that HSPA1B (1267)GG and HSPA1L (2437)CC genotypes were more frequent among preeclamptic than control patients, suggesting that these genotypes may play a role in the susceptibility for preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57461.RAvq6mNgAGq8J3tYV8tfH_58cGb9-G5Ro37RituwTq8Nw130_provenance.
- NP57463.RAvowEHJqy41LXs0WtNz46O9q85BtmzxkPt1R-VNcmTAk130_assertion description "[ Genetic variations in the IL-6 and IL-1ra gene identify IBD patients at risk for increased bone loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57463.RAvowEHJqy41LXs0WtNz46O9q85BtmzxkPt1R-VNcmTAk130_provenance.
- NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_assertion description "[ We concluded that HSPA1B (1267)GG and HSPA1L (2437)CC genotypes were more frequent among preeclamptic than control patients, suggesting that these genotypes may play a role in the susceptibility for preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57471.RAu02p3kNE17WSTwPl59LnbhPnQv2gBv191qELHOLGC6U130_provenance.
- NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_assertion description "[ Allele A of the Hsp70-2 gene may be associated with a less severe form of CD, suggesting the clinical value of the genotype assessment. The genetic determination of the defense mechanisms in CD appears to be associated with the polymorphism of the Hsp70-2 gene rather than that of the CD14 or IL-10 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57473.RAvl0U-ezQdnTTu92AtHoDRwWmTjxsAKnCA_GmEaJQEzg130_provenance.
- NP57474.RAnVs9kUkKqcavh5H8Az9NN6gXIkRkQOwmxBziSaTPUys130_assertion description "[ HSPA1B-179C>T is in linkage disequilibrium with HSPA1B1267A>G and is associated with variable production of HSPA1B and HSPA1A production. This suggests that HSPA1B-179C>T affects HSP70 production and is a key determinant of individual susceptibility to a variety of infectious and inflammatory diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57474.RAnVs9kUkKqcavh5H8Az9NN6gXIkRkQOwmxBziSaTPUys130_provenance.
- NP57476.RAhDda4pJtiI_6vUwi97gnVPwT3VjpOj8MoR9L7Ms78hY130_assertion description "[High frequencies of the HSP70-2 G and the TNF-alpha -308 A alleles were associated with risk of severe acute pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57476.RAhDda4pJtiI_6vUwi97gnVPwT3VjpOj8MoR9L7Ms78hY130_provenance.
- NP57481.RAjwabjMo0VrvKfon4yfHsM1qQGMs7-YyJuV9t8qNNICM130_assertion description "[Polymorphisms of heat shock protein 70 gene (HSPA1A, HSPA1B and HSPA1L) and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57481.RAjwabjMo0VrvKfon4yfHsM1qQGMs7-YyJuV9t8qNNICM130_provenance.
- NP57483.RAvWrrZEfhmZ37gBNIY0p7JC0PGDqcePI7hqm6X_yMCgU130_assertion description "[ We concluded that HSPA1B (1267)GG and HSPA1L (2437)CC genotypes were more frequent among preeclamptic than control patients, suggesting that these genotypes may play a role in the susceptibility for preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57483.RAvWrrZEfhmZ37gBNIY0p7JC0PGDqcePI7hqm6X_yMCgU130_provenance.
- NP57488.RAvIdngxMivkABOgbnsvSlJTC-dv95sKM3Gw77vEI_jgo130_assertion description "[A novel association between the human heat shock transcription factor 1 (HSF1) and prostate adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57488.RAvIdngxMivkABOgbnsvSlJTC-dv95sKM3Gw77vEI_jgo130_provenance.
- NP57491.RAueHUcqi_2vYXIVn7JG372l2siAzFvP2sqq0nyvitWeM130_assertion description "[Single and multigenic analysis of the association between variants in 12 steroid hormone metabolism genes and risk of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57491.RAueHUcqi_2vYXIVn7JG372l2siAzFvP2sqq0nyvitWeM130_provenance.
- NP57493.RAjveS-X246IomstGAcFTxMjGi8KU91TYcOYv6b2g-w4A130_assertion description "[In Caucasians, the HSD3B2 (TG)n,(TA)n,(CA)n intron 3 length polymorphism is associated with both prostate cancer risk and aggressiveness and the SRD5A2 V89L polymorphism may modify the risk conferred by this polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57493.RAjveS-X246IomstGAcFTxMjGi8KU91TYcOYv6b2g-w4A130_provenance.
- NP57498.RAqQnYQtuJNVzOQ8He2wKhpEJjqm7ZME6cbyQFyucTYm0130_assertion description "[To estimate the prostate cancer risk conferred by individual single nucleotide polymorphisms (SNPs), SNP-SNP interactions, and/or cumulative SNP effects, we evaluated the association between prostate cancer risk and the genetic variants of 12 key genes within the steroid hormone pathway (CYP17, HSD17B3, ESR1, SRD5A2, HSD3B1, HSD3B2, CYP19, CYP1A1, CYP1B1, CYP3A4, CYP27B1, and CYP24A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57498.RAqQnYQtuJNVzOQ8He2wKhpEJjqm7ZME6cbyQFyucTYm0130_provenance.
- NP57505.RAmnKJHtaPxWpQ44wNuga205buwhmFA0ok5Oyv7qsmnsU130_assertion description "[ Polymorphisms in HSD3B1, CYP19, AKR1C3 genes may be associated with an enlarged prostate in older men. These data provide insights into genes that should be examined further for their potential role in the pathogenesis of BPH. (c) 2005 Wiley-Liss, Inc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57505.RAmnKJHtaPxWpQ44wNuga205buwhmFA0ok5Oyv7qsmnsU130_provenance.
- NP57511.RAqi85cOkKgPIwpJ7meB2lPkSqLBlQBa3LwAiHHxUre54130_assertion description "[Although not able to demonstrate interaction models of SNPs, we provide evidence of HSD17 vlV A->C as a low penetrance genetic marker of endometriosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57511.RAqi85cOkKgPIwpJ7meB2lPkSqLBlQBa3LwAiHHxUre54130_provenance.
- NP57512.RAqtHwBZ6uLRJpcKSWHsV6Ztc6_0-I5XxAQFDPpZRTX8s130_assertion description "[Here, we evaluated whether the risk and severity of endometriosis are associated with polymorphisms in estradiol-synthesizing enzyme genes: the Ser312Gly polymorphism in 17-beta-hydroxysteroid dehydrogenase type 1 (HSD17B1) and the Arg264Cys polymorphism in cytochrome P450, subfamily XIX (CYP19).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57512.RAqtHwBZ6uLRJpcKSWHsV6Ztc6_0-I5XxAQFDPpZRTX8s130_provenance.
- NP57521.RAmgMLOxpSUYfdLwsMQBm41zPXIkf0eNof-MKWyAUEYww130_assertion description "[Possible difference in frequencies of genetic polymorphisms of estrogen receptor alpha, estrogen metabolism and P53 genes between estrogen receptor-positive and -negative breast cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57521.RAmgMLOxpSUYfdLwsMQBm41zPXIkf0eNof-MKWyAUEYww130_provenance.
- NP57526.RAuXjjTXi8QKZV7Z9p0azQqGcjTPMJpS_YZXS2zruIly8130_assertion description "[In conclusion, the I allele of ACE I/D polymorphism is significantly associated to salt-sensitive hypertension. The BP response to high salt intake was different among genotypes of ACE I/D and 11betaHSD G534A, suggesting that these polymorphisms may be potentially useful genetic markers of salt sensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57526.RAuXjjTXi8QKZV7Z9p0azQqGcjTPMJpS_YZXS2zruIly8130_provenance.
- NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_assertion description "[ Two different polymorphisms of the HSD11B2 gene were observed. The association of both polymorphisms was significantly higher in hypertensive subjects than in control subjects. Its role should be further investigated, but it could be related to other mutations in the promoter region of HSD11B2 or to the modulation of 11beta-HSD2 mRNA processing in hypertensive subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_provenance.
- NP57532.RArL0OEno72cOgIOBWG8CKqq_DDUN5S8P9VKzg8sx6dVg130_assertion description "[Genetic variations of HSD11B2 in hypertensive patients and in the general population, six rare missense/frameshift mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57532.RArL0OEno72cOgIOBWG8CKqq_DDUN5S8P9VKzg8sx6dVg130_provenance.
- NP57534.RAuwpa3ju1NBsPLQ5Xtr9FnSXjM-eLteAAHM1RDeB5FNc130_assertion description "[Genetic variation in 11beta-HSD1 contributes to enhanced cortisol clearance and compensatory adrenal hyperandrogenism in lean patients with PCOS but may be protective against obesity and some features of the metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57534.RAuwpa3ju1NBsPLQ5Xtr9FnSXjM-eLteAAHM1RDeB5FNc130_provenance.
- NP57555.RAsv9LzENnlcXnBk-xNDlsKgHfadKq8lwCB5-xPDZPKqY130_assertion description "[We can suppose that the `rare` alleles of HRas1 minisatellite are associated with increased risk of papillary thyroid cancer formation in children and adolescents after Chernobyl accident.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57555.RAsv9LzENnlcXnBk-xNDlsKgHfadKq8lwCB5-xPDZPKqY130_provenance.
- NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_assertion description "[These findings suggest that the influence of NAT2 genotype on AL and MF and its interaction with GSTM1 genotype may be dose dependent. The NAT2 slow genotype, in particular when combined with the GSTM1 null genotype, may confer increased susceptibility to adduct formation, gene mutation, and lung cancer when the smoking dose is low.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_provenance.
- NP57562.RAsHKgZnEEaq9-a7j0Xyb3zsvuzABcd7Sg-5Xzj9J4omc130_assertion description "[HPN is a likely candidate in prostate cancer susceptibility, as it encodes a transmembrane cell surface serum protease, which is overexpressed in prostate cancer; HPN is also located on 19q11-q13.2, where linkage is found with prostate cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57562.RAsHKgZnEEaq9-a7j0Xyb3zsvuzABcd7Sg-5Xzj9J4omc130_provenance.
- NP57563.RAs4Cy6tdNCo4cCGpwK_EOdl-EmgTgFnpskBuY3Ohx5Uk130_assertion description "[Germline genetic variation of HPN does not seem to contribute to risk of prostate cancer or prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57563.RAs4Cy6tdNCo4cCGpwK_EOdl-EmgTgFnpskBuY3Ohx5Uk130_provenance.
- NP57575.RAu4On2VeNCL5D3Zau7LL1MTsBrJ26nGgRmeKpf9MQjJA130_assertion description "[These comprised the germline c.242A>T (p.Glu81Val) missense mutation of HOXD4, detected in two children diagnosed with acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57575.RAu4On2VeNCL5D3Zau7LL1MTsBrJ26nGgRmeKpf9MQjJA130_provenance.
- NP57576.RAspoLh7LTqKyy15tW0n4gfSEehKQQK-Fmu0YNC3ZYv9E130_assertion description "[The G allele of the HOXA1 A218G polymorphism has been previously found associated with autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57576.RAspoLh7LTqKyy15tW0n4gfSEehKQQK-Fmu0YNC3ZYv9E130_provenance.
- NP57577.RAkO5HaQ9hgINZN6FZYo8-QFrG4TuyEL4kGgYBZ40SmB8130_assertion description "[Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57577.RAkO5HaQ9hgINZN6FZYo8-QFrG4TuyEL4kGgYBZ40SmB8130_provenance.
- NP57578.RAnsWN-FasN8j24TbBJ7Ir9XqLKXNK2a270WdVH3qm5J4130_assertion description "[Homeobox HOXA10 gene analysis in cryptorchidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57578.RAnsWN-FasN8j24TbBJ7Ir9XqLKXNK2a270WdVH3qm5J4130_provenance.
- NP57579.RApx3lghu5JtKeEWsmpG05ie-P8q2F2BnZUrl1Fll4YYU130_assertion description "[ The C314T mutation represents a common functional genetic polymorphism in the Chinese Han population with a variant T314 allele frequency similar to Japanese but lower than American Caucasians, whereas the A595G mutation does not appear to exist in this population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57579.RApx3lghu5JtKeEWsmpG05ie-P8q2F2BnZUrl1Fll4YYU130_provenance.