| 释义 |
- See also
- References
- Further reading
{{Infobox_gene}}Desmoglein-4 is a protein that in humans is encoded by the DSG4 gene.[1][2] See also - List of conditions caused by problems with junctional proteins
References1. ^{{cite journal |vauthors=Whittock NV, Bower C | title = Genetic evidence for a novel human desmosomal cadherin, desmoglein 4 | journal = J Invest Dermatol | volume = 120 | issue = 4 | pages = 523–30 |date=Mar 2003 | pmid = 12648213 | pmc = | doi = 10.1046/j.1523-1747.2003.12113.x }}
2. ^{{cite web | title = Entrez Gene: DSG4 desmoglein 4| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=147409| accessdate = }}
Further reading{{refbegin | 2}}- {{cite journal | author=Strausberg RL |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |name-list-format=vanc| author2=Feingold EA | author3=Grouse LH | display-authors=3 | last4=Derge | first4=JG | last5=Klausner | first5=RD | last6=Collins | first6=FS | last7=Wagner | first7=L | last8=Shenmen | first8=CM | last9=Schuler | first9=GD }}
- {{cite journal | author=Kljuic A |title=Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris |journal=Cell |volume=113 |issue= 2 |pages= 249–60 |year= 2003 |pmid= 12705872 |doi=10.1016/S0092-8674(03)00273-3 |name-list-format=vanc| author2=Bazzi H | author3=Sundberg JP | display-authors=3 | last4=Martinez-Mir | first4=Amalia | last5=O'Shaughnessy | first5=Ryan | last6=Mahoney | first6=My G | last7=Levy | first7=Moise | last8=Montagutelli | first8=Xavier | last9=Ahmad | first9=Wasim }}
- {{cite journal | author=Rafiq MA |title=A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis |journal=J. Invest. Dermatol. |volume=123 |issue= 1 |pages= 247–8 |year= 2004 |pmid= 15191570 |doi= 10.1111/j.0022-202X.2004.22715.x |name-list-format=vanc| author2=Ansar M | author3=Mahmood S | display-authors=3 | last4=Haque | first4=Sayedul | last5=Faiyaz-Ul-Haque | first5=Muhammad | last6=Leal | first6=Suzanne M. | last7=Ahmad | first7=Wasim }}
- {{cite journal | author=Gerhard DS |title=The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC) |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 |name-list-format=vanc| author2=Wagner L | author3=Feingold EA | display-authors=3 | last4=Shenmen | first4=CM | last5=Grouse | first5=LH | last6=Schuler | first6=G | last7=Klein | first7=SL | last8=Old | first8=S | last9=Rasooly | first9=R }}
- {{cite journal | author=Nagasaka T |title=Defining the pathogenic involvement of desmoglein 4 in pemphigus and staphylococcal scalded skin syndrome |journal=J. Clin. Invest. |volume=114 |issue= 10 |pages= 1484–92 |year= 2004 |pmid= 15545999 |doi= 10.1172/JCI20480 | pmc=525737 |name-list-format=vanc| author2=Nishifuji K | author3=Ota T | display-authors=3 | last4=Whittock | first4=NV | last5=Amagai | first5=M }}
- {{cite journal |vauthors=Bazzi H, Martinez-Mir A, Kljuic A, Christiano AM |title=Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats |journal=J. Investig. Dermatol. Symp. Proc. |volume=10 |issue= 3 |pages= 222–4 |year= 2006 |pmid= 16382669 |doi= 10.1111/j.1087-0024.2005.10110.x }}
- {{cite journal | author=Bazzi H |title=Desmoglein 4 is expressed in highly differentiated keratinocytes and trichocytes in human epidermis and hair follicle |journal=Differentiation |volume=74 |issue= 2–3 |pages= 129–40 |year= 2006 |pmid= 16533311 |doi= 10.1111/j.1432-0436.2006.00061.x |name-list-format=vanc| author2=Getz A | author3=Mahoney MG | display-authors=3 | last4=Ishida-Yamamoto | first4=Akemi | last5=Langbein | first5=Lutz | last6=Wahl | first6=James K. | last7=Christiano | first7=Angela M. }}
- {{cite journal | author=Wajid M |title=Localized autosomal recessive hypotrichosis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family |journal=J. Invest. Dermatol. |volume=127 |issue= 7 |pages= 1779–82 |year= 2007 |pmid= 17392831 |doi= 10.1038/sj.jid.5700791 |name-list-format=vanc| author2=Bazzi H | author3=Rockey J | display-authors=3 | last4=Lubetkin | first4=Jillian | last5=Zlotogorski | first5=Abraham | last6=Christiano | first6=Angela M }}
{{refend}}{{Cell adhesion molecules}}{{gene-18-stub}} |