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Research 31–60 of 159
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- Tissue expansion for correction of alopecia in a child with hypohidrotic ectodermal dysplasia
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib
- Involvement of Wnt, Eda and Shh at defined stages of sweat gland development
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Mesenchymal–epithelial interactions during hair follicle morphogenesis and cycling
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Dermatopathology and molecular genetics
- Combination of Transcriptomics and Proteomics Reveals Differentially Expressed Genes and Proteins in the Skin of EDAR Gene-Targeted and Wildtype Cashmere Goats
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Epidermal patterning and induction of different hair types during mouse embryonic development
- The developmental basis of fingerprint pattern formation and variation
- Morphogenesis, Growth Cycle and Molecular Regulation of Hair Follicles
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- Dermatological complications due to post‑COVID‑19 syndrome: A systematic review