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Research 91–120 of 1000+
- Voice changes in reproductive disorders, thyroid disorders and diabetes: a review
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Puberty induction with recombinant gonadotropin: What impact on future fertility?
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Testicular Steroidogenesis
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- New clinico‐genetic classification of trichothiodystrophy
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Birth Outcomes of Infants Born to Mothers with Alopecia Areata: A Nationwide Population-based Study in Korea
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Hair loss and its management in children
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Unruly hair
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion