The hairless promoter is differentially regulated by thyroid hormone in keratinocytes and neuroblastoma cellsENGELHARD, Andrew; CHRISTIANO, Angela M.Experimental dermatology. 2004, Vol 13, Num 4, pp 257-264, issn 0906-6705, 8 p.Article

Stem cells in the epidermisO'SHAUGHNESSY, Ryan F. L; CHRISTIANO, Angela M.Skin pharmacology and applied skin physiology. 2001, Vol 14, Num 6, pp 350-357, issn 1422-2868Article

Patterns of hairless (hr) gene expression in mouse hair follicle morphogenesis and cyclingPANTELEYEV, Andrei A; PAUS, Ralf; CHRISTIANO, Angela M et al.The American journal of pathology. 2000, Vol 157, Num 4, pp 1071-1079, issn 0002-9440Article

Hair on a gene string : recent advances in understanding the molecular genetics of hair lossIRVINE, Alan D; CHRISTIANO, Angela M.Clinical and experimental dermatology (Print). 2001, Vol 26, Num 1, pp 59-71, issn 0307-6938Article

A glycine substitution in the COL7A1 gene causes mild RDEB in a Pakistani familyKRAEMER, Liv; WAJID, Muhammad; CHRISTIANO, Angela M et al.EJD. European journal of dermatology. 2006, Vol 16, Num 6, pp 615-619, issn 1167-1122, 5 p.Article

A Nonsense Mutation in the SCN9A Gene in Congenital Insensitivity to PainKURBAN, Mazen; WAJID, Muhammad; SHIMOMURA, Yutaka et al.Dermatology (Basel). 2010, Vol 221, Num 2, pp 179-183, issn 1018-8665, 5 p.Article

Acne chlorina and acne vulgaris : casual likeness or causal homology?PANTELEYEV, Andrei A; THIEL, Renate; ROSENBACH, Thomas et al.Archives of dermatological research (Print). 2000, Vol 292, Num 11, pp 577-581, issn 0340-3696Article

Recapitulation of the hairless mouse phenotype using catalytic oligonucleotides: implications for permanent hair removalCSERHALMI-FRIEDMAN, Peter B; PANTELEYEV, Andrey A; CHRISTIANO, Angela M et al.Experimental dermatology. 2004, Vol 13, Num 3, pp 155-162, issn 0906-6705, 8 p.Article

Mutations in the Lipase H Gene Underlie Autosomal Recessive Woolly Hair/HypotrichosisSHIMOMURA, Yutaka; WAJID, Muhammad; PETUKHOVA, Lynn et al.Journal of investigative dermatology. 2009, Vol 129, Num 3, pp 622-628, issn 0022-202X, 7 p.Article

Evidence for a Founder Mutation in the Cathepsin C Gene in Three Families with Papillon-Lefèvre SyndromeKURBAN, Mazen; WAJID, Muhammad; SHIMOMURA, Yutaka et al.Dermatology (Basel). 2009, Vol 219, Num 4, pp 289-294, issn 1018-8665, 6 p.Article

Strategy to assess the efficiency of U1 RNA-hammerhead ribozyme constructs using GFP-tagged targetsCSERHALMI-FRIEDMAN, Peter B; DJABALI, Karima; DIETZ, Harry C et al.Experimental dermatology. 2003, Vol 12, Num 5, pp 712-715, issn 0906-6705, 4 p.Article

Clinical and molecular diagnostic criteria of congenital atrichia with papular lesionsZLOTOGORSKI, Abraham; PANTELEYEV, Andrei A; AITA, Vincent M et al.Journal of investigative dermatology. 2002, Vol 118, Num 5, pp 887-890, issn 0022-202XArticle

A missense mutation in the cadherin interaction site of the desmoglein 4 gene underlies localized autosomal recessive hypotrichosisMESSENGER, Andrew G; BAZZI, Hisham; PARSLEW, Richard et al.Journal of investigative dermatology. 2005, Vol 125, Num 5, pp 1077-1079, issn 0022-202X, 3 p.Article

Interaction of hairless and thyroid hormone receptor is not involved in the pathogenesis of atrichia with papular lesionsDJABALI, Karima; ZLOTOGORSKI, Abraham; METZKER, Arye et al.Experimental dermatology. 2004, Vol 13, Num 4, pp 251-256, issn 0906-6705, 6 p.Article

Clinical and molecular diagnostic criteria of congenital atrichia with papular lesionsZLOTOGORSKI, Abraham; PANTELEYEV, Andrei A; AITA, Vincent M et al.Journal of investigative dermatology. 2001, Vol 117, Num 6, pp 1662-1665, issn 0022-202XArticle

Novel Molecular Therapies for Heritable Skin DisordersUITTO, Jouni; CHRISTIANO, Angela M; IRWIN MCLEAN, W. H et al.Journal of investigative dermatology. 2012, Vol 132, Num 3, pp 820-828, issn 0022-202X, 9 p., 2Article

Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a ParadigmBETZ, Regina C; CABRAL, Rita M; CHRISTIANO, Angela M et al.Journal of investigative dermatology. 2012, Vol 132, Num 3, pp 906-914, issn 0022-202X, 9 p., 2Article

Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndromeCABRAL, Rita M; KURBAN, Mazen; WAJID, Muhammad et al.Genomics (San Diego, Calif.). 2012, Vol 99, Num 4, pp 202-208, issn 0888-7543, 7 p.Article

Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair TextureSHIMOMURA, Yutaka; WAJID, Muhammad; PETUKHOVA, Lynn et al.American journal of human genetics. 2010, Vol 86, Num 4, pp 632-638, issn 0002-9297, 7 p.Article

Identification of a novel splice site mutation in the human hairless gene underlying atrichia with papular lesionsPARADISI, Mauro; MASSE, Maureen; MARTINEZ-MIR, Amalia et al.EJD. European journal of dermatology. 2005, Vol 15, Num 5, pp 332-338, issn 1167-1122, 7 p.Article

The role of BMP signalling in the control of ID3 expression in the hair follicleO'SHAUGHNESSY, Ryan F. L; CHRISTIANO, Angela M; JAHODA, Colin A. B et al.Experimental dermatology. 2004, Vol 13, Num 10, pp 621-629, issn 0906-6705, 9 p.Article

Expression patterns of the transcription factor AP-2α during hair follicle morphogenesis and cyclingPANTELEYEV, Andrey A; MITCHELL, Pamela J; PAUS, Ralf et al.Journal of investigative dermatology. 2003, Vol 121, Num 1, pp 13-19, issn 0022-202X, 7 p.Article

An Unusual Case of Infiltrating Basal Cell CarcinomaSALAS-ALANIS, Julio Cesar; KURBAN, Mazen; CEPEDA-VALDES, Rodrigo et al.Dermatologic surgery. 2011, Vol 37, Num 9, pp 1316-1318, issn 1076-0512, 3 p.Article

Hereditary Leukonychia, or Porcelain Nails, Resulting from Mutations in PLCD1KIURU, Maija; KURBAN, Mazen; ITOH, Munenari et al.American journal of human genetics. 2011, Vol 88, Num 6, pp 839-844, issn 0002-9297, 6 p.Article

A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in miceFANTAUZZO, Katherine A; TADIN-STRAPPS, Marija; YUN YOU et al.Human molecular genetics (Print). 2008, Vol 17, Num 22, pp 3539-3551, issn 0964-6906, 13 p.Article