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Research 151–180 of 1000+
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Genetics of Alopecia
- Hypotrichosis in a child with olmsted syndrome
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Oral Presentations
- Lysophospholipid Mediators in Health and Disease
- Lrig1-expressing epidermal progenitors require SCD1 to maintain the dermal papilla niche
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- TRPV3 Ion Channel: From Gene to Pharmacology
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- Efficacy and safety of tofacitinib therapy in Asian patients with severe alopecia areata
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome