TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes.

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Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes.Advances in tryptophan hydroxylase-2 gene expression regulation: new insights into serotonin-stress interaction and clinical implications

P2860

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TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes.

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http://www.wikidata.org/entity/Q38272261

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2010 nî lūn-bûn

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2010年の論文

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2010年論文

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2010年論文

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TPH2 polymorphisms and express ...... th differing genetic subtypes.

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TPH2 polymorphisms and express ...... th differing genetic subtypes.

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TPH2 polymorphisms and express ...... th differing genetic subtypes.

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TPH2 polymorphisms and express ...... th differing genetic subtypes.

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Douglas C Bittel

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Merlin G Butler

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Rebecca S Henkhaus

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P2860

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology

The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C

Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome

Appetitive behavior, compulsivity, and neurochemistry in Prader-Willi syndrome.

Pharmacogenetics and the serotonin system: initial studies and future directions.

TPH2 and TPH1: association of variants and interactions with heroin addiction.

Psychiatric disorders in Prader-Willi syndrome: epidemiology and management.

Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome.

Characterization of a functional promoter polymorphism of the human tryptophan hydroxylase 2 gene in serotonergic raphe neurons.

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s11689-010-9051-6

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scholarly article

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10.1007/S11689-010-9051-6

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2010-05-21T00:00:00Z

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51840660

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3164046

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TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes.

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P2860

P2860

TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes.

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