Alternative splicing generates a secreted form of N-CAM in muscle and brain.
about
The poliovirus receptor protein is produced both as membrane-bound and secreted formsMutations in exon 3 of the glycogen debranching enzyme gene are associated with glycogen storage disease type III that is differentially expressed in liver and muscleA novel immediate-early response gene of endothelium is induced by cytokines and encodes a secreted proteinAt least 27 alternatively spliced forms of the neural cell adhesion molecule mRNA are expressed during rat heart developmentA novel mechanism for the regulation of amyloid precursor protein metabolismMembrane-anchored and soluble forms of betaglycan, a polymorphic proteoglycan that binds transforming growth factor-beta5'-Nucleotidase: molecular structure and functional aspectsNative avian c-erbB gene expresses a secreted protein product corresponding to the ligand-binding domain of the receptor.Transcription initiation sites and structural organization of the extreme 5' region of the rat neural cell adhesion molecule geneGenomes and proteomes: towards a multidimensional view of biology.Developmentally regulated expression of an exon containing a stop codon in the gene for glutamic acid decarboxylase.A ligand-free, soluble urokinase receptor is present in the ascitic fluid from patients with ovarian cancer.Myocardial localization and isoforms of neural cell adhesion molecule (N-CAM) in the developing and transplanted human heart.Localization of mRNA for neural cell adhesion molecule (N-CAM) polypeptides in neural and nonneural tissues by in situ hybridizationThe muscle specific domain of mouse N-CAM: structure and alternative splicing patterns.Enhanced expression of neural cell adhesion molecules and tenascin (cytotactin) during wound healing.Expression and localization of neural cell adhesion molecule and polysialic acid during chick corneal developmentNCAM1 association study of bipolar disorder and schizophrenia: polymorphisms and alternatively spliced isoforms lead to similarities and differences.The mouse neuronal cell surface protein F3: a phosphatidylinositol-anchored member of the immunoglobulin superfamily related to chicken contactin.Expression of the unique NCAM VASE exon is independently regulated in distinct tissues during development.Ca2+ influx and neurite growth in response to purified N-cadherin and lamininLAR tyrosine phosphatase receptor: alternative splicing is preferential to the nervous system, coordinated with cell growth and generates novel isoforms containing extensive CAG repeats.Olfactory neurons express a unique glycosylated form of the neural cell adhesion molecule (N-CAM).The axonally secreted protein axonin-1 is a potent substratum for neurite growth.smg mutants affect the expression of alternatively spliced SR protein mRNAs in Caenorhabditis elegans.N-myc down regulates neural cell adhesion molecule expression in rat neuroblastoma.Identification and structural characterization of a cDNA clone encoding a membrane-bound form of the polypeptide pheromone Er-1 in the ciliate protozoan Euplotes raikoviNovel Identity and Functional Markers for Human Corneal Endothelial Cells.Homophilic adhesion mediated by the neural cell adhesion molecule involves multiple immunoglobulin domainsSpecies- and tissue-specific expression of the C-terminal alternatively spliced form of the tumor suppressor p53.Alternative transcripts of the human CD23/Fc epsilon RII. A possible novel mechanism of generating a soluble isoform in the type-II cell surface receptor.Neuronal process outgrowth of human sensory neurons on monolayers of cells transfected with cDNAs for five human N-CAM isoforms.Removal of C6 astrocytoma cell surface molecules with phosphatidylinositol phospholipase C: effect on regulation of neural cell adhesion molecule isoforms.Expression of the cluster 1 antigen (neural cell adhesion molecule) in neuroectodermal tumours.Two alternatively spliced mouse urokinase receptor mRNAs with different histological localization in the gastrointestinal tract.Interactions of the neural cell adhesion molecule and the myelin-associated glycoprotein with collagen type I: involvement in fibrillogenesis.Purification and characterization of rat epididymal-fluid alpha-D-mannosidase: similarities to sperm plasma-membrane alpha-D-mannosidase.5'-Nucleotidases of chicken gizzard and human pancreatic adenocarcinoma cells are anchored to the plasma membrane via a phosphatidylinositol-glycanExpression of the natural killer (NK) cell-associated antigen CD56(Leu-19), which is identical to the 140-kDa isoform of N-CAM, in neural and skeletal muscle cells and tumors derived therefrom.Monoclonal antibody 3F8 recognises the neural cell adhesion molecule (NCAM) in addition to the ganglioside GD2.
P2860
Q24307688-F6FFAB84-87D1-4BCF-8B96-81372E448023Q24562068-761C520A-DFB1-45A3-877B-7F17C1326CBDQ24596894-879F4B9D-4C38-4065-ABCA-F7AAE2DC5268Q24607357-CAD78804-DC92-4A2D-8039-EBA652DC4360Q24674865-750F4802-195A-414A-A934-FD9104B08182Q24679265-ECFBB4FE-151F-4EB3-AFB7-75FF2A1CCF70Q28620587-F6C98BD3-DBAA-49BF-BA1F-46641BFD5FEFQ33244405-AEA8398F-3377-4A9A-B9DF-A5FEB0E38F97Q33255735-4BA93314-89EE-48B7-AF06-3106346DC91AQ33645263-DCAE37F5-1C06-48C9-BD4B-A5B03B4D1B6EQ33890475-0F536D6E-0380-4F83-B963-67910EBD4015Q33907027-1901E213-ED82-486C-BB9A-91355D5D6409Q34262060-FB5EA071-D859-4914-92F8-855BAB3256A1Q34324173-9618CFAB-1FCE-44E8-8DF1-178C4BE58FA0Q35779900-66EB026E-75A2-4F1F-8D2F-C69D725BB7DAQ35830730-F96BA2D4-6461-4F92-80C3-226D72E2154AQ35921432-C95BB528-1BF5-4F59-B43F-4198266936EFQ36140914-1919CBFC-498E-48D1-9D25-98D226EC106EQ36221337-36E082F9-7426-440A-AF2E-DA4756C59EB8Q36224017-AD0EAE1E-0BED-4939-AF94-27DDC2B1BAAEQ36234917-670DABAF-887D-4623-927D-7C8B959BCFFFQ36235220-32A7A2AF-E0E0-465F-85EE-14779D8C82B9Q36383474-721E3474-695E-4BEE-A974-39D58EFA80D9Q36529155-A5029487-4782-4BF3-A53D-C78E7CCC404BQ36574846-15199C86-429F-4CD7-BF80-9FE23FC58072Q36708061-ED438969-F292-4720-94AC-83693D20EF59Q36873105-F9A32E64-405A-405F-8A9A-E98902E3605BQ36944541-610A0BDF-F1C6-45E3-9326-E9F0FA6A38D9Q37628776-36418203-A5A5-4CDF-AE59-5A3AFE9A3164Q40396261-63344854-1037-43EB-9D12-1D7BF52951E4Q41513560-C1833BF7-6F78-417B-8980-9D390C6700B5Q41583555-A3527261-B1C0-432D-81C5-FA0163D71D1DQ41676002-9AF64CE4-890A-4825-A764-2251F3243D46Q41680687-A4A02D71-5858-49EE-841B-33FDC5234EE2Q41877722-E73441AD-ABAD-454F-9734-C016F7CBE388Q41881514-BB59BC2F-3A34-4F25-A167-BD3211AC8D15Q41901436-1B222784-6130-4E24-B03F-AF43D97F4573Q41956237-84C516F4-26D8-49D8-97DA-C2CCC27B716CQ41958489-E9A1E82C-71AE-4A7C-8B27-D1E8CCC0C331Q42055221-56C1685B-ADFE-4D03-B3E8-19E13DD8E53C
P2860
Alternative splicing generates a secreted form of N-CAM in muscle and brain.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年学术文章
@wuu
1988年学术文章
@zh-cn
1988年学术文章
@zh-hans
1988年学术文章
@zh-my
1988年学术文章
@zh-sg
1988年學術文章
@yue
1988年學術文章
@zh
1988年學術文章
@zh-hant
name
Alternative splicing generates a secreted form of N-CAM in muscle and brain.
@en
Alternative splicing generates a secreted form of N-CAM in muscle and brain.
@nl
type
label
Alternative splicing generates a secreted form of N-CAM in muscle and brain.
@en
Alternative splicing generates a secreted form of N-CAM in muscle and brain.
@nl
prefLabel
Alternative splicing generates a secreted form of N-CAM in muscle and brain.
@en
Alternative splicing generates a secreted form of N-CAM in muscle and brain.
@nl
P2093
P1433
P1476
Alternative splicing generates a secreted form of N-CAM in muscle and brain.
@en
P2093
Thompson J
P304
P356
10.1016/0092-8674(88)90241-3
P407
P577
1988-12-01T00:00:00Z