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Abbreviation : HR
Long Form : hairless gene
No. Year Title Co-occurring Abbreviation
2019 Hairless regulates p53 target genes to exert tumor suppressive functions in glioblastoma. GBM
2018 Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers. ---
2016 Disease causing homozygous variants in the human hairless gene. APL
2016 Identification of mutations in U2HR in two Chinese families with Marie Unna hereditary hypotrichosis. MUHH
2013 Atrichia with papular lesions in a chinese family caused by novel compound heterozygous mutations and literature review. APL
2012 Identification of a novel U2HR mutation c.14C>T in a Chinese patient with Marie Unna hereditary hypotrichosis. MUHH, ORF
2010 Marie Unna hereditary hypotrichosis: a Turkish family with loss of eyebrows and a U2HR mutation. MUHH
2010 Molecular basis for hair loss in mice carrying a novel nonsense mutation (Hrrh-R ) in the hairless gene (Hr). rh-R
2009 Alopecia: association with resistance to thyroid hormones. AA, RTH, TRbeta
10  2007 Alopecia areata in a rhesus monkey (Macaca mulatta). ---
11  2007 Identification of mutations in the human hairless gene in two new families with congenital atrichia. APL
12  2004 A new allele of the mouse hairless gene interferes with Hox/LacZ transgene regulation in hair follicle primordia. NIMR
13  2004 Interaction of hairless and thyroid hormone receptor is not involved in the pathogenesis of atrichia with papular lesions. APL, TRID2
14  2004 The hairless promoter is differentially regulated by thyroid hormone in keratinocytes and neuroblastoma cells. ---
15  2003 Compound heterozygosity for mutations in the hairless gene causes atrichia with papular lesions. ---
16  2003 Linkage mapping of the porcine hairless gene (HR ) to chromosome 14. ---
17  2002 The Charles River "hairless" rat mutation maps to chromosome 1: allelic with fuzzy and a likely orthologue of mouse frizzy. CR, fr, fz
18  2002 The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach. AGA, SSCA, TDT
19  2001 Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene. ---
20  2000 A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family. HMU
21  1999 Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family. ---