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Research 811–840 of 1000+
- In vivo function of VDR in gene expression-VDR knock-out mice
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Generalized atrophic benign epidermolysis bullosa.
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- Autotaxin-LPA signaling contributes to obesity-induced insulin resistance in muscle and impairs mitochondrial metabolism
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Differential sensitivity of epidermal cell subpopulations to β-catenin-induced ectopic hair follicle formation
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- A kindred with mutant IKAROS and autoimmunity
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Genetically separable determinants of hair keratin gene expression
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Real-world single-center experience with 10 cases of generalized pustular psoriasis successfully treated with ixekizumab
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Participation of CD34-enriched mouse adipose cells in hair morphogenesis
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Risk of autoimmune diseases in patients with RASopathies: systematic study of humoral and cellular immunity
- Skin morphology of the mutant hairless USP mouse
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Establishment of Tsc2-deficient rat embryonic stem cells