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Research 781–810 of 1000+
- Visualising Androgen Receptor Activity in Male and Female Mice
- Application of lncRNA-miRNA-mRNA ceRNA network analysis in the treatment of androgenic alopecia.
- 766 H3K9me3 methyltransferase SETDB1 controls retrotransposon silencing, DNA methylation, constitutive heterochromatin maintenance and 3D-chromatin structure in epidermal keratinocytes
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Genetic Basis of Male Pattern Baldness
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Cultivation of Hair Matrix Cells from Cashmere Goat Skins and Exemplified Applications
- Ancestral Diversity of Skin Reaches Single-Cell Resolution
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- P78 Acrodermatitis enteropathica in children: clinical cases
- The Case | Bilateral kidney tumors and lung cysts
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- The Skin Microbiome: Current Landscape and Future Opportunities
- Molecular Evolution and Protein Structure Variation of Dkk Family
- Genetic Disorders and Defects in Vitamin D Action
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Thymosin β4 promotes angiogenesis, wound healing, and hair follicle development
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome