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Research 61–90 of 1000+
- <i>WNT10A</i> , dermatology and dentistry
- Genetic Susceptibility to Alopecia
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Identification of a Cyclosporine-Specific P450 Hydroxylase Gene through Targeted Cytochrome P450 Complement (CYPome) Disruption in Sebekia benihana
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- The urine as a diagnostic key for a homozygous EGFR mutation
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- The Genetics of Human Skin Disease
- Morpho-Regulation of Ectodermal Organs
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes
- Progeroide Syndrome
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- 9. Immunology and Genetics
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine