Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse.

DNA sequencing with chain-terminating inhibitors

1977 • 69,181 citations

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1975 • 33,059 citations

A conserved AU sequence from the 3′ untranslated region of GM-CSF mRNA mediates selective mRNA degradation

1986 • 4,200 citations

The scanning model for translation: an update.

1989 • 3,525 citations

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

1983 • 1,481 citations

Identification and localization of synaptophysin, an integral membrane glycoprotein of Mr 38,000 characteristic of presynaptic vesicles

1985 • 1,425 citations

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

1990 • 1,032 citations

Splicing of Messenger RNA Precursors

1987 • 919 citations

Splicing of Messenger RNA Precursors

1984 • 874 citations

A 38,000-dalton membrane protein (p38) present in synaptic vesicles.

1985 • 856 citations

The LDL Receptor Gene: A Mosaic of Exons Shared with Different Proteins

1985 • 845 citations

Protein p38: an integral membrane protein specific for small vesicles of neurons and neuroendocrine cells.

1986 • 671 citations

Report of the committee on the genetic constitution of the X chromosome (Part 1 of 3)

1990 • 597 citations

Synapsins: Mosaics of Shared and Individual Domains in a Family of Synaptic Vesicle Phosphoproteins

1989 • 535 citations

Mutation in LDL Receptor: Alu-Alu Recombination Deletes Exons Encoding Transmembrane and Cytoplasmic Domains

1985 • 453 citations

Congenital Stationary Night Blindness With Negative Electroretinogram

1986 • 439 citations

Identification of Synaptophysin as a Hexameric Channel Protein of the Synaptic Vesicle Membrane

1988 • 356 citations

Molecular characterization of synaptophysin, a major calcium-binding protein of the synaptic vesicle membrane.

1986 • 296 citations

Synaptophysin: molecular organization and mRNA expression as determined from cloned cDNA.

1987 • 205 citations

Synaptophysin expression during synaptogenesis in the rat cerebellar cortex

1989 • 204 citations

Synaptophysin is targeted to similar microvesicles in CHO and PC12 cells.

1989 • 157 citations

Transmembrane Topography and Evolutionary Conservation of Synaptophysin

1989 • 153 citations

Protein tyrosine phosphorylation in synaptic vesicles.

1988 • 148 citations

Cloning and sequence analysis of cDNA encoding p38, a major synaptic vesicle protein.

1987 • 128 citations

The structure of the human synapsin I gene and protein.

1990 • 107 citations

Microvesicles of the neurohypophysis are biochemically related to small synaptic vesicles of presynaptic nerve terminals.

1989 • 105 citations

The multisubunit structure of synaptophysin. Relationship between disulfide bonding and homo-oligomerization.

1990 • 104 citations

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

1979 • 99 citations

Synaptophysin: A sensitive and specific marker for ganglion cells in central nervous system neoplasms

1990 • 98 citations

Topogenesis and sorting of synaptophysin: Synthesis of a synaptic vesicle protein from a gene transfected into nonneuroendocrine cells

1989 • 96 citations

Chromosomal Mapping of Genes Involved in Growth Control

1986 • 91 citations

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

1986 • 90 citations

Congenital stationary night blindness

1977 • 73 citations

Börjeson‐Forssman‐Lehmann syndrome: Clinical manifestations and gene localization to Xq26‐27

1989 • 69 citations

Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.

1988 • 64 citations

Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation

1987 • 64 citations

Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3

1989 • 64 citations

Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13.

1989 • 61 citations

A non‐syndromal form of X‐linked mental retardation (XLMR) is linked to DXS14

1988 • 60 citations

A primary genetic map of the pericentromeric region of the human X chromosome

1988 • 59 citations

Linkage analysis suggests at least two loci for X‐linked nonspecific mental retardation

1988 • 54 citations

The cDNA and derived amino acid sequences for rat and human synaptophysin

1987 • 53 citations

Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation.

1990 • 53 citations

Markers for Neuroendocrine Differentation

1988 • 49 citations

Regional localization of the TIMP gene on the human X chromosome

1989 • 45 citations

Two different genes for X-linked retinitis pigmentosa

1988 • 43 citations

The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22?q24) by somatic cell hybrid analysis and in situ hybridization

1986 • 42 citations

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

1987 • 41 citations

Linkage localization of Börjeson‐Forssman‐Lehmann syndrome

1989 • 40 citations

Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.

1985 • 38 citations

Postnatal development of protein P-38 (‘synaptophysin’) immunoreactivity in pontine and medullary gustatory zones of rat

1989 • 34 citations

Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome

1990 • 29 citations

Expression of synaptophysin and neuron‐specific enolase during neuronal differentiation in vitro: Effects of dimethyl sulfoxide

1989 • 29 citations

Norrie disease: Linkage analysis using a 4.2-kb RFLP detected by a human ornithine aminotransferase cDNA probe

1989 • 13 citations