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Research 511–540 of 1000+
- Mutant Cx43 in Skin Differentiation and Disease
- What causes acne inversa (or hidradenitis suppurativa)? – The debate continues
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- [Netherton's syndrome in two sisters].
- A case of congenital pili multigemini
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Ritlecitinib and brepocitinib demonstrate significant improvement in scalp alopecia areata biomarkers
- Continuous MEK inhibition by AZD6244 (ARRY-142886) results in exhaustion of the cutaneous keratinocytic stem cell pool and resembles senescence driven skin aging
- Alopecia areata: current concepts
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- A case of familial trichomegaly with synophrys in association with loose anagen syndrome
- Double mutation of <i>claudin‐1</i> and <i>claudin‐3</i> causes alopecia in infant mice
- Viewpoint 4
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Telogen effluvium and associated incidence of abnormal serum ferritin, zinc, 25-hydroxy vitamin D, and thyroid-stimulating hormone
- Trichoscopy update 2011
- Congenital hypotrichosis due to short anagen
- Hormone und Haarwachstum
- Short anagen syndrome in an African American woman