115 related articles for article (PubMed ID: 18273904)
1. Erythrocyte dematin is a candidate gene for Marie Unna hereditary hypotrichosis and related hairloss disorders.
Mohseni M; Chishti AH
Am J Hematol; 2008 May; 83(5):430-2. PubMed ID: 18273904
[No Abstract] [Full Text] [Related]
2. Combined deletion of mouse dematin-headpiece and beta-adducin exerts a novel effect on the spectrin-actin junctions leading to erythrocyte fragility and hemolytic anemia.
Chen H; Khan AA; Liu F; Gilligan DM; Peters LL; Messick J; Haschek-Hock WM; Li X; Ostafin AE; Chishti AH
J Biol Chem; 2007 Feb; 282(6):4124-35. PubMed ID: 17142833
[TBL] [Abstract][Full Text] [Related]
3. Marie Unna hereditary hypotrichosis gene maps to human chromosome 8p21 near hairless.
Sreekumar GP; Roberts JL; Wong CQ; Stenn KS; Parimoo S
J Invest Dermatol; 2000 Mar; 114(3):595-7. PubMed ID: 10777357
[No Abstract] [Full Text] [Related]
4. Loss of heterozygosity on 8p in prostate cancer implicates a role for dematin in tumor progression.
Lutchman M; Pack S; Kim AC; Azim A; Emmert-Buck M; van Huffel C; Zhuang Z; Chishti AH
Cancer Genet Cytogenet; 1999 Nov; 115(1):65-9. PubMed ID: 10565303
[TBL] [Abstract][Full Text] [Related]
5. Isoform cloning, actin binding, and chromosomal localization of human erythroid dematin, a member of the villin superfamily.
Azim AC; Knoll JH; Beggs AH; Chishti AH
J Biol Chem; 1995 Jul; 270(29):17407-13. PubMed ID: 7615546
[TBL] [Abstract][Full Text] [Related]
6. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.
Cichon S; Kruse R; Hillmer AM; Kukuk G; Anker M; Altland K; Knapp M; Propping P; Nöthen MM
Br J Dermatol; 2000 Oct; 143(4):811-4. PubMed ID: 11069461
[TBL] [Abstract][Full Text] [Related]
7. Headpiece domain of dematin is required for the stability of the erythrocyte membrane.
Khanna R; Chang SH; Andrabi S; Azam M; Kim A; Rivera A; Brugnara C; Low PS; Liu SC; Chishti AH
Proc Natl Acad Sci U S A; 2002 May; 99(10):6637-42. PubMed ID: 12011427
[TBL] [Abstract][Full Text] [Related]
8. Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.
He PP; Zhang XJ; Yang Q; Li M; Liang YH; Yang S; Yan KL; Cui Y; Shen YY; Wang HY; Sun LD; Du WH; Shen YJ; Xu SJ; Huang W
Br J Dermatol; 2004 May; 150(5):837-42. PubMed ID: 15149494
[TBL] [Abstract][Full Text] [Related]
9. Alternative splicing and structure of the human erythroid dematin gene.
Kim AC; Azim AC; Chishti AH
Biochim Biophys Acta; 1998 Jul; 1398(3):382-6. PubMed ID: 9655941
[TBL] [Abstract][Full Text] [Related]
10. Membrane-actin microfilament connections: an increasing diversity of players related to band 4.1.
Arpin M; Algrain M; Louvard D
Curr Opin Cell Biol; 1994 Feb; 6(1):136-41. PubMed ID: 8167019
[TBL] [Abstract][Full Text] [Related]
11. Progressive patterned scalp hypotrichosis, with wiry hair, onycholysis, and intermittently associated cleft lip and palate: clinical and genetic distinction from Marie Unna.
Green J; Fitzpatrick E; de Berker D; Forrest SM; Sinclair RD
J Investig Dermatol Symp Proc; 2003 Jun; 8(1):121-5. PubMed ID: 12895008
[TBL] [Abstract][Full Text] [Related]
12. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis.
Lefevre P; Rochat A; Bodemer C; Vabres P; Barrandon Y; de Prost Y; Garner C; Hovnanian A
Eur J Hum Genet; 2000 Apr; 8(4):273-9. PubMed ID: 10854110
[TBL] [Abstract][Full Text] [Related]
13. Identification of a novel locus for Marie Unna hereditary hypotrichosis to a 17.5 cM interval at 1p21.1-1q21.3.
Yang S; Gao M; Cui Y; Yan KL; Ren YQ; Zhang GL; Wang PG; Xiao FL; Du WH; Liang YH; Sun LD; Xu SJ; Huang W; Zhang XJ
J Invest Dermatol; 2005 Oct; 125(4):711-4. PubMed ID: 16185270
[TBL] [Abstract][Full Text] [Related]
14. The gene encoding the erythrocyte membrane skeleton protein dematin (Epb4.9) maps to mouse chromosome 14.
Peters LL; Eicher EM; Azim AC; Chishti AH
Genomics; 1995 Apr; 26(3):634-5. PubMed ID: 7607697
[No Abstract] [Full Text] [Related]
15. The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.
van Steensel M; Smith FJ; Steijlen PM; Kluijt I; Stevens HP; Messenger A; Kremer H; Dunnill MG; Kennedy C; Munro CS; Doherty VR; McGrath JA; Covello SP; Coleman CM; Uitto J; McLean WH
Am J Hum Genet; 1999 Aug; 65(2):413-9. PubMed ID: 10417283
[TBL] [Abstract][Full Text] [Related]
16. Dematin exhibits a natively unfolded core domain and an independently folded headpiece domain.
Chen L; Jiang ZG; Khan AA; Chishti AH; McKnight CJ
Protein Sci; 2009 Mar; 18(3):629-36. PubMed ID: 19241372
[TBL] [Abstract][Full Text] [Related]
17. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
Spiegl B; Hundeiker M
Fortschr Med; 1979 Nov; 97(44):2018-22. PubMed ID: 511082
[TBL] [Abstract][Full Text] [Related]
18. A phosphorylation-induced conformation change in dematin headpiece.
Jiang ZG; McKnight CJ
Structure; 2006 Feb; 14(2):379-87. PubMed ID: 16472756
[TBL] [Abstract][Full Text] [Related]
19. Marie Unna hereditary hypotrichosis.
Argenziano G; Sammarco E; Rossi A; Delfino M; Calvieri S
Eur J Dermatol; 1999 Jun; 9(4):278-80. PubMed ID: 10356404
[TBL] [Abstract][Full Text] [Related]
20. Dematin interacts with the Ras-guanine nucleotide exchange factor Ras-GRF2 and modulates mitogen-activated protein kinase pathways.
Lutchman M; Kim AC; Cheng L; Whitehead IP; Oh SS; Hanspal M; Boukharov AA; Hanada T; Chishti AH
Eur J Biochem; 2002 Jan; 269(2):638-49. PubMed ID: 11856323
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]