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Research 31–60 of 1000+
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Vitamin D metabolism and function in the skin
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Biology and Genetics of Hair
- Dermatopathology and molecular genetics
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Diagnostic Value of VDR in Bone Metastasis and Prognosis of Patients with Breast Cancer and Expression Correlation between Vitamin D Receptor and Hairless Protein
- Le gène<i>hairless</i>de la souris
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- 毛乳頭細胞と毛包上皮細胞間の細胞内・細胞外情報伝達
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Two females with hair loss
- Critical Appraisal of Reports on the Treatment of Perioral Dermatitis