Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1 (Q24320046)

GOA release 2020-03-11

signal transduction

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GOA release 2020-03-11

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3

S Jozwiak

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author name string

E P Henske

1

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M P Short

2

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C M Bovey

4

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S Ramlakhan

5

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J L Haines

6

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D J Kwiatkowski

Tyrosine phosphorylation of the vav proto-oncogene product in activated B cells

7

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language of work or name

English

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publication date

January 1995

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published in

Annals of Human Genetics

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volume

59

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issue

Pt 1

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page(s)

25-37

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cites work

1 reference

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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 April 2017

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An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

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Strategies for multilocus linkage analysis in humans

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Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

21 April 2017

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Nonsense mutations in the human beta-globin gene affect mRNA metabolism

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Exon amplification: a strategy to isolate mammalian genes based on RNA splicing

21 January 2018

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Product of vav proto-oncogene defines a new class of tyrosine protein kinase substrates

21 January 2018

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Premature translation termination mediates triosephosphate isomerase mRNA degradation

21 January 2018

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Four novel FBN1 mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndrome

21 January 2018

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Identification and characterization of the tuberous sclerosis gene on chromosome 16

21 January 2018

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Interleukin-2 induces tyrosine phosphorylation of the vav proto-oncogene product in human T cells: lack of requirement for the tyrosine kinase lck.

21 January 2018

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Phenotypes of the tuberous sclerosis complex with a revision of diagnostic criteria

21 January 2018

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Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients.

21 January 2018

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A radiation-reduced hybrid cell line containing 5 Mb/17 cM of human DNA from 9q34

21 January 2018

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Unequal expression of NF1 alleles.

21 January 2018

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Vav: a potential link between tyrosine kinases and ras-like GTPases in hematopoietic cell signaling

21 January 2018

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Loss of the amino-terminal helix-loop-helix domain of the vav proto-oncogene activates its transforming potential

21 January 2018

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Identification of the von Hippel-Lindau disease tumor suppressor gene

21 January 2018

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Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

21 January 2018

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor.

21 January 2018

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Analysis of mutations at the neurofibromatosis 1 (NF1) locus

21 January 2018

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Nonsense mutations in the dihydrofolate reductase gene affect RNA processing

21 January 2018

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Inhibition of hematopoietic development from embryonic stem cells by antisense vav RNA.

21 January 2018

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7 January 2021

A high-resolution linkage map of human 9q34.1.

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7 January 2021

EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9

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7 January 2021

Linkage of tuberous sclerosis to ABO blood group

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7 January 2021

Nonsense mutations and diminished mRNA levels

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7 January 2021

Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994.

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7 January 2021

Pathology of tuberous sclerosis. Neuropathologic aspects

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7 January 2021

Cellular neuropathology of tuberous sclerosis

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7 January 2021

Genetic Heterogeneity in Tuberous Sclerosis. Study of a Large Collaborative Dataset

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7 January 2021

Tyrosine kinase-stimulated guanine nucleotide exchange activity of Vav in T cell activation

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7 January 2021

Cardiac rhabdomyomata in tuberous sclerosis: their course and diagnostic value

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7 January 2021

Cardiac rhabdomyomas and their association with tuberous sclerosis

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7 January 2021

Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, 11q, and 12q. The Tuberous Sclerosis Collaborative Group

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7 January 2021

Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis

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7 January 2021

Diagnostic criteria: tuberous sclerosis complex. Report of the Diagnostic Criteria Committee of the National Tuberous Sclerosis Association

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7 January 2021