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Research 91–120 of 1000+
- Hairless: A nuclear receptor corepressor essential for skin function
- Parallel Independent Losses of G-Type Lysozyme Genes in Hairless Aquatic Mammals
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Le gène<i>hairless</i>de la souris
- Atrichia with papular lesions
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Reply
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Nevus comedonicus with lesional growth of terminal hair: An unusual case
- A homozygous single T deletion found in the GGCX gene with PXE-like phenotypes
- Dermatopathology and molecular genetics
- Biology and Genetics of Hair
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- Molecular basis of congenital atrichia in humans and mice.
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- ATRICHIA WITH PAPULAR LESIONS – A CASE REPORT
- Genetics of Alopecia
- Congenital Atrichia: A Case Report
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Pair Annotation: Adaption of Pair Programming to Corpus Annotation
- Activation of β-catenin signaling programs embryonic epidermis to hair follicle fate
- Congenital atrichia with papular lesions
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs