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WW domains
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
review article
1 reference
stated in
Europe PubMed Central
title
WW domains
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
author name string
Staub O
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
Rotin D
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
publication date
1 May 1996
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
published in
Structure
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
volume
4
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
page(s)
495-499
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
cites work
WWP, a new amino acid motif present in single or multiple copies in various proteins including dystrophin and the SH3-binding Yes-associated protein YAP65
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The WW domain: a signalling site in dystrophin?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The rsp5-domain is shared by proteins of diverse functions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protein modules and signalling networks
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A phosphotyrosine interaction domain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of a novel protein-binding module--the WW domain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The WW domain of Yes-associated protein binds a proline-rich ligand that differs from the consensus established for Src homology 3-binding modules
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two binding orientations for peptides to the Src SH3 domain: development of a general model for SH3-ligand interactions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An SH3 binding region in the epithelial Na+ channel (alpha rENaC) mediates its localization at the apical membrane
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Formin binding proteins bear WWP/WW domains that bind proline-rich peptides and functionally resemble SH3 domains
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a set of genes with developmentally down-regulated expression in the mouse brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NPl1, an essential yeast gene involved in induced degradation of Gap1 and Fur4 permeases, encodes the Rsp5 ubiquitin-protein ligase.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SPT3 interacts with TFIID to allow normal transcription in Saccharomyces cerevisiae
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Synaptotagmin I is a high affinity receptor for clathrin AP-2: implications for membrane recycling
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary structure of the uracil transport protein of Saccharomyces cerevisiae.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
GAP1, the general amino acid permease gene of Saccharomyces cerevisiae. Nucleotide sequence, protein similarity with the other bakers yeast amino acid permeases, and nitrogen catabolite repression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and characterization of the dystrophin anchoring site on beta-dystroglycan
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A rat brain mRNA encoding a transcriptional activator homologous to the DNA binding domain of retroviral integrases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The regions of the Fe65 protein homologous to the phosphotyrosine interaction/phosphotyrosine binding domain of Shc bind the intracellular domain of the Alzheimer's amyloid precursor protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CD45 protein-tyrosine phosphatase associates with the WW domain-containing protein, CD45AP, through the transmembrane region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of the sites of interaction between lymphocyte phosphatase-associated phosphoprotein (LPAP) and CD45
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0969-2126%2896%2900054-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0969-2126(96)00054-8
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
PubMed ID
8736547
1 reference
stated in
Europe PubMed Central
PubMed ID
8736547
retrieved
26 September 2017
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