5 results for author:"Escamez M.J." in Literature citations
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| Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex. Garcia M., Santiago J.L., Terron A., Hernandez-Martin A., Vicente A., Fortuny C., De Lucas R., Lopez J.C., Cuadrado-Corrales N., Holguin A. et al. Br. J. Dermatol. 165:683-692(2011) · Mapped (2) |
| A prevalent mutation with founder effect in Spanish Recessive Dystrophic Epidermolysis Bullosa families. Cuadrado-Corrales N., Sanchez-Jimeno C., Garcia M., Escamez M.J., Illera N., Hernandez-Martin A., Trujillo-Tiebas M.J., Ayuso C., Del Rio M. BMC Med. Genet. 11:139-139(2010) · Mapped (2) |
| The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutation. Escamez M.J., Garcia M., Cuadrado-Corrales N., Llames S.G., Charlesworth A., De Luca N., Illera N., Sanchez-Jimeno C., Holguin A., Duarte B. et al. Br. J. Dermatol. 163:155-161(2010) · Mapped (2) |
| Novel human pathological mutations. Gene symbol: COL7A1. Disease: Epidermolysis bullosa dystrophica. Garcia M., Escamez M.J., Cuadrado-Corrales N., Sanchez-Jimeno C., Illera N., Lopez-Martinez M.A., Trujillo-Tiebas M.J., Ayuso C., Del Rio M. Hum. Genet. 127:116-117(2010) · UniProtKB (1) |
| In vitro and in vivo wound healing-promoting activities of human cathelicidin LL-37. Carretero M., Escamez M.J., Garcia M., Duarte B., Holguin A., Retamosa L., Jorcano J.L., Rio M.D., Larcher F. J. Invest. Dermatol. 128:223-236(2008) · Mapped (2) |