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Research 691–720 of 1000+
- Delayed Puberty
- Prostate cancer and androgenic alopecia
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- National scientific medical meeting 1996 abstracts
- Polycystic Ovary Syndrome
- Transforming growth factor-β in stem cells and tissue homeostasis
- Obesity and the skin
- Polycystic Ovarian Syndrome
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Morpho‐regulation in diverse chicken feather formation: Integrating branching modules and sex hormone‐dependent morpho‐regulatory modules
- Differential impact of environmental factors on systemic and localized autoimmunity
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- Quoi de neuf en recherche dermatologique ?
- Gender Differences in Production and Circulating Levels of Sex Hormones and Their Impact on Aging Skin
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- Selection signatures for fiber production in commercial species: A review
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Decay of Skin-Specific Gene Modules in Pangolins
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants