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Research 331–360 of 1000+
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Runx3 is involved in hair shape determination
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Stem cells in embryonic skin development
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation.
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- The exposome impact on hair health: etiology, pathogenesis and clinical features ‒ Part I
- Immunological control of skin development: from homeostasis to developmental pathologies
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Notch Signaling in Hair Follicle Development
- Phospholipase C‐δ1 is an essential molecule downstream of <i>Foxnl,</i> the gene responsible for the nude mutation, in normal hair development
- CRISPR/Cas9: A Promising Approach for Alopecia
- Sostdc1 defines the size and number of skin appendage placodes
- Lipoatrophy and severe metabolic disturbance in mice with fat-specific deletion of PPARγ
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Relation of Skin Polyamines to the Hairless Phenotype in Transgenic Mice Overexpressing Spermidine/Spermine N1-Acetyltransferase
- Alternative uses of dermoscopy in daily clinical practice: An update
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Bubble hair and other acquired hair shaft anomalies due to hot ironing on wet hair
- Anaesthetics and platelets.
- Loss of epidermal PLCg1 induced sebaceous gland hyperplasia and sparse hair
- Hormonal acne: leading to a paradigm shift in the management of acne
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Molecular basis of hypohidrotic ectodermal dysplasia: an update