Search
for
Sort by
Research 181–210 of 1000+
- Comparing Current Therapeutic Modalities of Androgenic Alopecia: A Literature Review of Clinical Trials
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Topical Finasteride: A Comprehensive Review of Androgenetic Alopecia Management for Men and Women
- Androgenetic alopecia
- Cross-section trichometry, a clinical tool for assessing the progression and treatment response of alopecia
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Thyroid hormone action on skin.
- Progeroide Syndrome
- News in brief
- Melanocytes: The new Black
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Defects in mitochondrial DNA replication and oxidative damage in muscle of mtDNA mutator mice
- An Overview of Analeptic Applications of Omega-3 Fatty Acids
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Congenital atrichia with papular lesions
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Lactate in skin homeostasis: metabolism, skin barrier, and immunomodulation
- Frontal fibrosing alopecia, just lichen planopilaris?
- Regulatory Effects of Thai Rice By-Product Extracts from Oryza sativa L. cv. Bue Bang 3 CMU and Bue Bang 4 CMU on Melanin Production, Nitric Oxide Secretion, and Steroid 5α-Reductase Inhibition
- Skin bacteriota ameliorates androgenetic alopecia via harmonizing skin immuno inflammatory balance
- Combined Physicochemical and Transcriptomic Analyses Reveal the Effect of Black Wolfberry Ferment on Alopecia
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Convergent evolution has led to the loss of claw proteins in snakes and worm lizards
- Vitamin D and Human Health: Lessons from Vitamin D Receptor Null Mice
- A mutation in MAP2 is associated with prenatal hair follicle density
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- 男性型脱毛症の原因についての手がかり