Search
for
Sort by
Research 31–60 of 1000+
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Genetic Hair Disorders: A Review
- Hair Shaft Dysplasias
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- 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
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Hair loss in children.
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Hair follicles and their role in skin health
- Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Alopecia in Epidermolysis Bullosa
- Unruly hair
- Diseases of Periocular Hair
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Hair Loss in Children
- Disorders of the skin appendages
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways