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Research 31–60 of 218
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Clinical Snippets
- Clinical Snippets
- Alopezien und Hypotrichosen im Kindesalter
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Value of dermoscopy for the diagnosis of monilethrix
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Genetics of Structural Hair Disorders
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Inherited Disorders of the Hair
- Biology and Genetics of Hair
- Combined hormonal contraception and venous thromboembolism
- Diagnosis and treatments of hirsutism: where are we?
- Current Genetics in Hair Diseases
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Keratins: the hair shaft's backbone revealed
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives