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Research 361–390 of 1000+
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- Scalp Microbiota Dysbiosis in Seborrheic Alopecia and Restoration Following Herbal Extract Shampoo Intervention
- Th,-e mechanistic insights into the application of retinoids and possible adjunct therapeutic treatment to androgenic alopecia
- Study on the Efficacy and Potential Mechanism of Topical Shen Bai Hair Growing Decoction against Androgenetic Alopecia Based on Ultrahigh Performance Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry and RNA-seq
- Epidemiology and Treatment of Male Androgenetic Alopecia
- A randomized double blind study of the effect of finasteride on hair growth in male patients of androgenetic alopecia
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Genetic Hair Disorders: A Review
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- A missense mutation in Lama3 causes androgen alopecia
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Do Changes in Chromosomes Cause Aging?
- Myotonic Dystrophy—A Progeroid Disease?
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Rapamycin but not acarbose decreases age-related loss of outer hair cells in the mouse Cochlea
- Monilethrix in three generations
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Renal tubular dysfunction presenting as recurrent hypokalemic periodic quadriparesis in systemic lupus erythematosus