(Q48254101)

10 February 2018

title

Developmental and tissue expression patterns of mouse Mpp4 gene (English)

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10 February 2018

author

Colin J. Barnstable

series ordinal

3

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10 February 2018

author name string

Man Li

series ordinal

1

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10 February 2018

Samuel Shao-Min Zhang

series ordinal

2

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10 February 2018

language of work or name

English

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publication date

1 July 2003

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10 February 2018

Biochemical and Biophysical Research Communications

published in

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10 February 2018

volume

307

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10 February 2018

issue

2

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10 February 2018

page(s)

229-235

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10 February 2018

Signaling pathways are focused at specialized regions of the plasma membrane by scaffolding proteins of the MAGUK family

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Intramolecular interactions regulate SAP97 binding to GKAP

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GKAP, a novel synaptic protein that interacts with the guanylate kinase-like domain of the PSD-95/SAP90 family of channel clustering molecules

7 January 2021

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rDLG6: a novel homolog of Drosophila DLG expressed in rat brain

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Spatial distribution of mDLG6 mRNA in embryonic and adult mouse brain

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Cloning and characterization of the human retina-specific gene MPP4, a novel member of the p55 subfamily of MAGUK proteins.

7 January 2021

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Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa.

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Sonic hedgehog mediates the polarizing activity of the ZPA

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Expression of the growth cone specific epitope CDA 1 and the synaptic vesicle protein SVP38 in the developing mammalian cerebral cortex.

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Transgenic expression of the jellyfish green fluorescent protein in the cone photoreceptors of the mouse

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

7 January 2021

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Synaptogenesis in the photoreceptor terminal of the mouse retina

7 January 2021

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Developmental expression pattern of phototransduction components in mammalian pineal implies a light-sensing function

7 January 2021

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PDZ proteins organize synaptic signaling pathways

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PDZ domains in synapse assembly and signalling

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DLG differentially localizes Shaker K+-channels in the central nervous system and retina of Drosophila

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Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

7 January 2021

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An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

7 January 2021

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10.1016/S0006-291X(03)01142-2

7 January 2021

Identifiers

DOI

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10 February 2018

1 reference

10 February 2018