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Research 181–210 of 1000+
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Smad7-Induced β-Catenin Degradation Alters Epidermal Appendage Development
- Hidradenitis Suppurativa: From Physiopathologies to Targeted Therapeutics
- Hidradenitis Suppurativa: From Physiopathologies to Targeted Therapeutics
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Recent advances in the epidermal growth factor receptor/ligand system biology on skin homeostasis and keratinocyte stem cell regulation
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Differential cutaneous wound healing in thermally injured MRL/MPJ mice
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- 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
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Androgen Receptor–Mediated Paracrine Signaling Induces Regression of Blood Vessels in the Dermal Papilla in Androgenetic Alopecia
- Double mutation of <i>claudin‐1</i> and <i>claudin‐3</i> causes alopecia in infant mice
- Nevus Comedonicus (Blaschkoid Variant)
- Immunological control of skin development: from homeostasis to developmental pathologies
- Color Doppler Ultrasound Pattern of Cutaneous Exosomes at High and Ultra-High Frequency.
- Atrichia with papular lesions mimicking alopecia areata universalis
- LB1011 Oncogenic ras mutation induces spatiotemporally specific tissue deformation through converting fluctuated into sustained ERK activation
- Loose anagen syndrome in one identical twin girl
- 1336 The de novo DNA methyltransferase DNMT3A is required for epidermal homeostasis