(Q34421778)

2 August 2017

title

Sequence, splice site and population frequency distribution analyses of the polymorphic human tryptophan hydroxylase intron 7. (English)

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2 August 2017

4

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2 August 2017

5

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2 August 2017

Nielsen DA

1

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2 August 2017

Jenkins GL

series ordinal

2

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2 August 2017

Stefanisko KM

series ordinal

3

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2 August 2017

language of work or name

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1 April 1997

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2 August 2017

published in

Molecular Brain Research

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2 August 2017

volume

45

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2 August 2017

issue

1

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2 August 2017

page(s)

145-148

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5-HIAA in the cerebrospinal fluid. A biochemical suicide predictor?

2 August 2017

cites work

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Transcription factors and the regulation of haemopoiesis: lessons from GATA and SCL proteins.

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Complete coding sequence of human tryptophan hydroxylase

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Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A

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In vivo mutation at the human HPRT locus

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Cooperation of pre-mRNA sequence elements in splice site selection

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cis and trans regulation of tissue-specific transcription

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Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with tourette syndrome

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Estimation of linkage disequilibrium in randomly mating populations

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Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene

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The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences

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Mapping of the serotonin 5-HT1D beta autoreceptor gene on chromosome 6 and direct analysis for sequence variants.

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7 January 2021

Identification, expression, and pharmacology of a Cys23-Ser23 substitution in the human 5-HT2c receptor gene (HTR2C)

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7 January 2021

A catalogue of splice junction sequences

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Two naturally occurring amino acid substitutions in the human 5-HT1A receptor: glycine 22 to serine 22 and isoleucine 28 to valine 28.

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Suicidality and 5-Hydroxyindoleacetic Acid Concentration Associated With a Tryptophan Hydroxylase Polymorphism

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7 January 2021

SSCP primer design based on single-strand DNA structure predicted by a DNA folding program

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7 January 2021

Polymorphism in serotonin transporter gene associated with susceptibility to major depression.

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7 January 2021

Mapping of the serotonin 5-HT1D alpha autoreceptor gene (HTR1D) on chromosome 1 using a silent polymorphism in the coding region.

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7 January 2021

Splicing of messenger RNA precursors

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7 January 2021

The genetic basis of complex human behaviors

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Distinct binding specificities and functions of higher eukaryotic polypyrimidine tract-binding proteins

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7 January 2021

10.1016/S0169-328X(96)00304-X

Identifiers

DOI

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2 August 2017

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