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Research 271–300 of 1000+
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- <i>Msx2</i> Prevents Stratified Squamous Epithelium Formation in the Enamel Organ
- Genetics of Structural Hair Disorders
- Perspectives on Hair Evolution Based on Some Comparative Studies on Vertebrate Cornification
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Molecular Genetics of Alopecias
- A newborn presenting with congenital blistering
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- A procedure for the culture of hair follicles as functionally intact organoids
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Alopezien und Hypotrichosen im Kindesalter
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Current Genetics in Hair Diseases
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Dynamic analysis of skin transcriptome in Xinjiang goats and functional verification of ELOVL3 in dermal papilla cell proliferation
- Whole transcriptome sequencing of different hair types in inner Mongolian cashmere goats
- 260 Anti-OX40 monoclonal antibody IMG-007 exhibited clinical activity of hair regrowth, suppressed scalp inflammatory biomarkers in patients with severe alopecia areata in a Ph1b/2a study
- Effects of FGF5-mediated LncRNA on the skin fibroblast growth of Liaoning Cashmere goats
- The Naked (N) Mutation, Chromosome 15
- Few Simple Sequence Repeats in Human Hair
- Hair Anomalies in a 6-Year-Old Girl
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Epidermolysis bullosa in calves in the United Kingdom
- Transcriptomic Analysis Provides Molecular Insights into Skin Development in Dezhou Donkey Foals
- 591 Chromatin architectural protein CTCF regulates terminal keratinocyte differentiation in the developing epidermis and hair follicles
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs