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Research 121–150 of 1000+
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Hirsutism: diagnosis and treatment
- Female Adolescent Hair Disorders
- Laser Hair Reduction and Removal
- Evaluación de la seguridad de minoxidil oral a dosis bajas en el tratamiento de la alopecia
- MINOXIDIL IN RESISTANT HYPERTENSION
- Drug-Induced Hair Disorders
- Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III
- Minoxidil in Severe Hypertension
- The effects of topical diazoxide on hair follicular growth and physiology of the stumptailed macaque
- Low-dose oral minoxidil for treating alopecia: A 3-year North American retrospective case series
- Minoxidil-induced hypertrichosis: Pathophysiology, clinical implications, and therapeutic strategies
- Cutaneous Side Effects of Chemotherapy and Radiotherapy
- Hair and scalp disorders
- Pathologies of the skin and its appendages in endocrine diseases
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- An evaluation of the safety and efficacy of bimatoprost for eyelash growth in pediatric subjects
- The Dark Side of Gefitinib: Reflectance Confocal Microscopy Applied to Hair Hyperpigmentation
- Madarosis: A marker of many Maladies
- Genetic Hair Disorders: A Review