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Research 181–210 of 1000+
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- The stem cell quiescence and niche signaling is disturbed in the hair follicle of the hairpoor mouse, an MUHH model mouse
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Roles of MED1 in Quiescence of Hair Follicle Stem Cells and Maintenance of Normal Hair Cycling
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Monilethrix in three generations
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- The stiffness of the extracellular matrix is a key factor in tumor progression
- Focal Dermal Hypoplasia Associated With Lymphedema: A Case Report From Saudi Arabia
- An eruption of numerous spiny papules in a pediatric transplant patient
- A rare hair loss in children: Monilethrix
- Budesonide for maintenance of remission in Crohn's disease
- Epidermal Vascular Endothelial Growth Factor Production Is Required for Permeability Barrier Homeostasis, Dermal Angiogenesis, and the Development of Epidermal Hyperplasia
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Ear pinna growth and differentiation is conserved in murids and requires BMP signaling for chondrocyte proliferation
- Zebrafish Model of Hereditary Pigmentary Disorders
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Zinc and Zinc Transporters in Dermatology
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Historical Archives
- The histopathologic spectrum of psoriasis
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Gender Differences in Cardiac Hypertrophy