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Research 421–450 of 1000+
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis
- [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
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- 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
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Advanced Medical Therapies in the Management of Non-Scarring Alopecia: Areata and Androgenic Alopecia
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Development and homeostasis of the sebaceous gland
- Double mutation of <i>claudin‐1</i> and <i>claudin‐3</i> causes alopecia in infant mice
- Viewpoint 4
- Alopecia in Rhesus macaques correlates with immunophenotypic alterations in dermal inflammatory infiltrates consistent with hypersensitivity etiology
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- A case of familial trichomegaly with synophrys in association with loose anagen syndrome
- Congenital hypotrichosis due to short anagen
- Hormone und Haarwachstum
- Hyperplasia of the Subcutaneous Adipose Tissue Is the Primary Histopathologic Abnormality in Lipedematous Scalp
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- CD44 signaling in skin wound healing and regeneration
- Myeloproliferative disorder associated with alopecia universalis