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Research 31–60 of 1000+
- <i>WNT10A</i> , dermatology and dentistry
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Store-operated calcium channels in skin
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Congenital atrichia and hypotrichosis
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Hair Shaft Dysplasias
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Genetic Hair Disorders: A Review
- Unruly hair
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Evaluating the Role of Thyroid Stimulating Hormone and Ferritin Levels with Hair Loss among Patients with COVID-19: Case-Control Study
- Molecular Mechanisms Regulating Hair Follicle Development
- Hair loss in children.
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- 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
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Whole blood transcriptome profiling identifies candidate genes associated with alopecia in male giant pandas (Ailuropoda melanoleuca)
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep