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Research 601–630 of 1000+
- Hair shaft structures in EDAR induced ectodermal dysplasia
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Decades of progressive red and yellow nodules
- Testosterone and dihydrotestosterone production in genetically furless and furred male rabbits and effects on growth.
- Molecular mechanisms of androgenetic alopecia
- Family History and Risk of Hair Loss
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Clinical Research Progress on Plum-Blossom Needle Combined Therapy for Androgenic Alopecia
- In vivo hair growth-promoting efficacies of herbal extracts and their cubosomal suspensions
- An Ayurvedic Approach to Palitya (Premature Greying of Hair)