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Research 151–180 of 1000+
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Pathogenesis of androgenetic alopecia
- DNCB 유발 피부염 생쥐에서 탄닌이 피부조직 모발주기 관련 유전자 발현에 미치는 영향
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Nonhuman primate dermatology: a literature review
- Skin Development and Disease: A Molecular Perspective
- Ophthalmologic Comorbidities in Alopecia Areata
- Congenital atrichia associated with nevus flammeus: A rare association
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Madarosis: A marker of many Maladies
- Alopecia areata – Current understanding and management
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Treatment options for androgenetic alopecia: Efficacy, side effects, compliance, financial considerations, and ethics
- Immunological and Metabolic Causes of Infertility in Polycystic Ovary Syndrome
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Biomedical Technologies for Androgenic Alopecia Treatment: Advance, Mechanism and Future Direction
- E-Poster
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS