Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Daniel Tattersall"'
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Biomembranes. 1818(8):1952-1961
The expression of multiple connexin (Cx) types in the epidermis, their differential expression during wound closure and the association of skin pathology with specific Cx gene mutations, are indicative of important functions for Cxs in the skin. In t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b692bcf5481863ecf3a5e18601d008e3
Publikováno v:
Human Molecular Genetics
The epidermis expresses a number of connexin (Cx) proteins that are implicated in gap junction-mediated cell communication. Distinct dominantly inherited mutations in Cx31 cause the skin disease erythrokeratoderma variabilis (EKV) and hearing loss wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::617f991f61d22970ca5cf46dfab38b4c
https://doi.org/10.1093/hmg/ddp436
https://doi.org/10.1093/hmg/ddp436
Publikováno v:
The American Journal of Pathology. 174:970-978
One of the primary functions of skin is to form a defensive barrier against external infections and water loss. Disrupted barrier function underlies the most severe and often lethal form of recessive congenital ichthyosis, harlequin ichthyosis (HI).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1021eab2fbc022ebd49461d4befa460a
https://doi.org/10.2353/ajpath.2009.080860
https://doi.org/10.2353/ajpath.2009.080860
Publikováno v:
Traffic. 8:1873-1886
Endosome-to-Golgi retrieval of the cation-independent mannose 6-phosphate receptor (CIMPR) requires the function of the retromer complex. Retromer is localized to endosomes and comprises two distinct sub complexes: the vacuolar protein sorting 35/29/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24d42c04974ec221f79fa50e88bafacf
https://doi.org/10.1111/j.1600-0854.2007.00652.x
https://doi.org/10.1111/j.1600-0854.2007.00652.x
Autor:
Michael A. Curtis, Harshad Navsaria, Daniel Tattersall, Annie Papakonstantinopoulou, Claire A. Scott, Anna C. Thomas, Daniel J. Jagger, Jiehan Chong, Caroline Trolove, Drashnika Patel, Y. K. Stella Man, David P. Kelsell, Edel A. O'Toole
Publikováno v:
Journal of Membrane Biology. 218:29-37
A large proportion of recessive nonsyndromic hearing loss is due to mutations in the GJB2 gene encoding connexin 26 (Cx26), a component of a gap junction. Within different ethnic groups there are specific common recessive mutations, each with a relat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4de832464a466043df1ef51feaaf640
https://doi.org/10.1007/s00232-007-9025-0
https://doi.org/10.1007/s00232-007-9025-0
Autor:
Rita M, Cabral, Daniel, Tattersall, Vishal, Patel, Graham D, McPhail, Elizabeth, Hatzimasoura, Dominic J, Abrams, Andrew P, South, David P, Kelsell
Publikováno v:
Journal of cell science. 125(Pt 12)
Desmosomes are intercellular junctions specialised for strong adhesion that are prominent in the epidermis and heart muscle. Defective desmosomal function due to inherited mutations in the constitutive desmosomal gene desmoplakin (DSP) causes skin or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::792e9a6db0ef7d00fb5297dbb74159b2
https://pubmed.ncbi.nlm.nih.gov/22454510
https://pubmed.ncbi.nlm.nih.gov/22454510
Autor:
Daniel Tattersall, Dominic Abrams, Vishal Patel, Rita M. Cabral, Elizabeth Hatzimasoura, David P. Kelsell, Andrew P. South, Graham D. McPhail
Publikováno v:
Journal of Cell Science.
Desmosomes are intercellular junctions specialised for strong adhesion that are prominent in the epidermis and heart muscle. Defective desmosomal function due to inherited mutations in the constitutive desmosomal gene desmoplakin (DSP) causes skin or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de43290e884371c5030a7e6f283444af
https://doi.org/10.1242/jcs.084152
https://doi.org/10.1242/jcs.084152
Retromer is a membrane-associated heteropentameric coat complex that functions in the endosome-to-Golgi retrieval of the cation-independent mannose-6-phosphate receptor, the Wntless protein and other membrane proteins of physiological significance. R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d12a40d1d5f8defc9b4dd0895b928c3b
https://europepmc.org/articles/PMC2704877/
https://europepmc.org/articles/PMC2704877/
The retromer complex is a conserved cytoplasmic coat complex that mediates the endosome-to-Golgi retrieval of vacuole/lysosome hydrolase receptors in yeast and mammals. The recognition of cargo proteins by the retromer is performed by the Vps35p/VPS3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5013af96ef91077143a95456eb81e002
https://europepmc.org/articles/PMC2267345/
https://europepmc.org/articles/PMC2267345/
Publikováno v:
Biochemical Journal; 2007, Vol. 408 Issue 2, p287-295, 9p