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Research 91–120 of 1000+
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Genetic Hair Disorders: A Review
- Eyebrow Loss
- TONGUE, RED
- Follicular unit extraction [FUE] – One procedure, many uses
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Madarosis: A marker of many Maladies
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- Oral Presentations
- British Association of Dermatologists living guideline for managing people with alopecia areata 2024
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Diseases of Hair
- Diseases of Hair
- Current Genetics in Hair Diseases
- Alopecia in Children
- British Association of Dermatologists living guideline for managing people with alopecia areata 2025