Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes. - Wikidata - wikimedia - TriplyDB

Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.

Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.

http://www.wikidata.org/entity/Q37407692

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Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse A third member of the synapsin gene family A melanocyte-specific gene, Pmel 17, maps near the silver coat color locus on mouse chromosome 10 and is in a syntenic region on human chromosome 12 Molecular characterization and chromosomal mapping of melanoma growth stimulatory activity, a growth factor structurally related to beta-thromboglobulin The human U1-70K snRNP protein: cDNA cloning, chromosomal localization, expression, alternative splicing and RNA-binding Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13 Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM Structure and functional expression of the human macrophage inflammatory protein 1 alpha/RANTES receptor Molecular cloning, functional expression, and chromosomal localization of mouse hepatocyte nuclear factor 1 Impairment of axonal development and of synaptogenesis in hippocampal neurons of synapsin I-deficient mice A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11.A view of interphase chromosomes.Polymorphic X-chromosome inactivation of the human TIMP1 gene.A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes.Porcine synapsin 1: SYN1 gene analysis and functional characterization of the promoter.Multiple synapsin I messenger RNAs are differentially regulated during neuronal development.2012 William Allan Award: Adventures in cytogenetics.The C allele of synonymous SNP (rs1142636, Asn170Asn) in SYN1 is a risk factor for the susceptibility of Korean female schizophrenia.Family MRX9 revisited: further evidence for locus heterogeneity in MRX.Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13.

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P2860

Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.

http://www.wikidata.org/entity/Q37407692

description

1986 nî lūn-bûn

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1986年の論文

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1986年学术文章

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1986年学术文章

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1986年学术文章

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1986年学术文章

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1986年学术文章

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1986年學術文章

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1986年學術文章

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1986年學術文章

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name

Genes for synapsin I, a neuron ...... uman and murine X chromosomes.

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Genes for synapsin I, a neuron ...... uman and murine X chromosomes.

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type

label

Genes for synapsin I, a neuron ...... uman and murine X chromosomes.

@en

Genes for synapsin I, a neuron ...... uman and murine X chromosomes.

@nl

prefLabel

Genes for synapsin I, a neuron ...... uman and murine X chromosomes.

@en

Genes for synapsin I, a neuron ...... uman and murine X chromosomes.

@nl

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PNAS.83.22.8679

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Proceedings of the National Academy of Sciences of the United States of America

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Genes for synapsin I, a neuron ...... uman and murine X chromosomes.

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L J DeGennaro

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T L Yang-Feng

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U Francke

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P2860

Synapsin I (protein I), a nerve terminal-specific phosphoprotein. III. Its association with synaptic vesicles studied in a highly purified synaptic vesicle preparation

Synapsin I (protein I), a nerve terminal-specific phosphoprotein. I. Its general distribution in synapses of the central and peripheral nervous system demonstrated by immunofluorescence in frozen and plastic sections

Gene mapping in Mus musculus by interspecific cell hybridization: assignment of the genes for tripeptidase-1 to chromosome 10, dipeptidase-2 to chromosome 18, acid phosphatase-1 to chromosome 12, and adenylate kinase-1 to chromosome 2

Assignment of the gene for cytoplasmic superoxide dismutase (Sod-1) to a region of chromosome 16 and of Hprt to a region of the X chromosome in the mouse

Comparative gene mapping: order of loci on the X chromosome is different in mice and humans

X chromosome-linked muscular dystrophy (mdx) in the mouse

Molecular cloning of cDNAs for the nerve-cell specific phosphoprotein, synapsin I.

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.

Human luteinizing hormone-releasing hormone gene (LHRH) is located on short arm of chromosome 8 (region 8p11.2----p21).

On a unusual brain atrophy syndrome in hyperammonemia in childhood

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