Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
暂无分享,去创建一个
Yang Liu | Sen Yang | Miao Sun | Sven Cichon | Marcel Huber | Christine Bodemer | Li Jiang | Markus M Nöthen | Alain Hovnanian | Amy S Paller | S. Cichon | M. Nöthen | C. Bodemer | Xuejun Zhang | D. Hohl | A. Paller | A. Messenger | A. Hovnanian | A. Terrinoni | Li Jiang | Sen Yang | C. Munro | Y. Wen | Yang Liu | Yiming Xu | Yiwei Zhao | R. Hua | Kai-bo Wang | Miao Sun | Yuanhong Li | R. Kruse | R. Betz | M. Steensel | M. Geel | P. Steijlen | M. Huber | G. Dunnill | C. Kennedy | Y. Prost | A. Irvine | Rod Sinclair | Jack Green | D. Shang | Qing Liu | Yang Luo | Hong-Duo Chen | W. H. Lo | W. McLean | Chun-di He | Xue Zhang | Xue-Jun Zhang | Xue Zhang | Peter M Steijlen | Chun-Di He | Daniel Hohl | Alan D Irvine | Yiwei Zhao | Colin S Munro | Michel van Geel | Yuanhong Li | Andrew Messenger | Alessandro Terrinoni | Regina C Betz | Xue Zhang | Qing Liu | Yiming Xu | Dandan Shang | Rui Hua | Yaran Wen | W H Irwin McLean | Kaibo Wang | Roland Kruse | Maurice A M van Steensel | Giles S Dunnill | Cameron Kennedy | Yves de Prost | Rod Sinclair | Jack Green | Yang Luo | Hong-Duo Chen | Wilson H-Y Lo | Yaran Wen | X. Zhang | W. Lo | Hong-duo Chen | W. Mclean | Xue-Jun Zhang | Alan D. Irvine | Xuejun Zhang | Hong Duo Chen | Chun Di He | Xue Zhang
[1] G. Scheper,et al. Translation matters: protein synthesis defects in inherited disease , 2007, Nature Reviews Genetics.
[2] Mayumi Ito,et al. Wnt-dependent de novo hair follicle regeneration in adult mouse skin after wounding , 2007, Nature.
[3] G. Beaudoin,et al. Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation , 2006, Cell cycle.
[4] G. Cotsarelis. Epithelial stem cells: a folliculocentric view. , 2006, The Journal of investigative dermatology.
[5] M. Sachs,et al. Downstream control of upstream open reading frames. , 2006, Genes & development.
[6] G. Beaudoin,et al. Hairless triggers reactivation of hair growth by promoting Wnt signaling. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[7] Liangdan Sun,et al. Identification of a novel locus for Marie Unna hereditary hypotrichosis to a 17.5 cM interval at 1p21.1-1q21.3. , 2005, The Journal of investigative dermatology.
[8] Igor B. Rogozin,et al. Evolutionary conservation suggests a regulatory function of AUG triplets in 5′-UTRs of eukaryotic genes , 2005, Nucleic acids research.
[9] Graziano Pesole,et al. uAUG and uORFs in human and rodent 5'untranslated mRNAs. , 2005, Gene.
[10] Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1·1‐cM interval at 8p21.3 , 2004, The British journal of dermatology.
[11] Lin Chang-min,et al. Beta-catenin controls hair follicle morphogenesis and stem cell differentiation , 2004 .
[12] E. Fearon,et al. Transient activation of beta -catenin signaling in cutaneous keratinocytes is sufficient to trigger the active growth phase of the hair cycle in mice. , 2003, Genes & development.
[13] E. Fuchs,et al. Stem cells in the skin: waste not, Wnt not. , 2003, Genes & development.
[14] S. Millar,et al. WNT signals are required for the initiation of hair follicle development. , 2002, Developmental cell.
[15] G. Beaudoin,et al. The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor. , 2001, Genes & development.
[16] R. Happle,et al. Guess what! Hypotrichosis congenita of Marie Unna: comment. , 2001, European journal of dermatology : EJD.
[17] W. Birchmeier,et al. β-Catenin Controls Hair Follicle Morphogenesis and Stem Cell Differentiation in the Skin , 2001, Cell.
[18] A. Christiano,et al. Patterns of hairless (hr) gene expression in mouse hair follicle morphogenesis and cycling. , 2000, The American journal of pathology.
[19] S. Cichon,et al. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family , 2000, The British journal of dermatology.
[20] M. Cazzola,et al. Translational pathophysiology: a novel molecular mechanism of human disease. , 2000, Blood.
[21] C. Bodemer,et al. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis , 2000, European Journal of Human Genetics.
[22] G. Sreekumar,et al. Marie Unna hereditary hypotrichosis gene maps to human chromosome 8p21 near hairless. , 2000, The Journal of investigative dermatology.
[23] R Paus,et al. The biology of hair follicles. , 1999, The New England journal of medicine.
[24] R. Paus,et al. What controls hair follicle cycling? , 1999, Experimental dermatology.
[25] H. Kremer,et al. The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing. , 1999, American journal of human genetics.
[26] R. Bergman,et al. Identification of a genetic defect in the hairless gene in atrichia with papular lesions: evidence for phenotypic heterogeneity among inherited atrichias. , 1999, American journal of human genetics.
[27] David Hogg,et al. Mutation of the CDKN2A 5' UTR creates an aberrant initiation codon and predisposes to melanoma , 1999, Nature Genetics.
[28] S. Cichon,et al. Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia. , 1998, Human molecular genetics.
[29] J. Ott,et al. Alopecia universalis associated with a mutation in the human hairless gene. , 1998, Science.
[30] R. Skoda,et al. An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia , 1998, Nature Genetics.