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Research 331–360 of 1000+
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor
- Retinoids: Compounds important to hair growth
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- MmuPV1-Induced Cutaneous Squamous Cell Carcinoma Arises Preferentially from Lgr5+ Epithelial Progenitor Cells
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Iperplasia Collaterale Nella Oncogenesi Sperimentale Del Ratto: Rilievi in corso di trattamento con Vitamina A
- Trichothiodystrophy
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Atrichia With Papular Lesions
- Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable association.
- [Trichothiodystrophy: a morphological and biochemical study].
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Genetics of Structural Hair Disorders
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Dermatopathology and molecular genetics
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Epidermal field carcinogenesis in bald-headed: An attempt at finetuning early non-invasive detection
- Small molecules facilitate single factor-mediated sweat gland cell reprogramming
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- The fundamentals of WNT10A
- Generalized Congenital Hypotrichosis in a Female Rottweiler
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Noninflammatory, Nonpruritic Alopecia of Horses
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- [Sodium valproate-induced kinky hair].