Search
for
Sort by
Research 871–900 of 1000+
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Decorin-mediated dermal papilla cell-derived exosomes regulate hair follicle growth and development through miR-129-2-3p/SMAD3/TGF-β axis
- Structural perspectives on the androgen receptor, the elusive shape-shifter
- Tinea captitis due to Microsporum ferrugineum: A case of unusual laboratory finding on direct microscopic examination of infected hairs and skin lesions
- Abstract 4350: Pharmacodynamic biomarkers: Evaluation of oncology drug target engagement in human plucked scalp and beard hair
- Mouse notch: expression in hair follicles correlates with cell fate determination.
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Characterization and expression analysis of KAP7.1, KAP8.2 gene in Liaoning new-breeding cashmere goat hair follicle
- Molecular cloning of two novel types of peptidylarginine deiminase cDNAs from retinoic acid‐treated culture of a newborn rat keratinocyte cell line
- Cloning of human, murine, and marsupial keratin 7 and a survey of K7 expression in the mouse
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- 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>)
- Microbiome in the hair follicle of androgenetic alopecia patients
- The Genetics of Human Skin Disease
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Hair After Death
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Syntaxin 9 is Enriched in Skin Hair Follicle Epithelium and Interacts With the Epidermal Growth Factor Receptor
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Exact, time-independent estimation of clone size distributions in normal and mutated cells
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Identification of functional circRNAs regulating ovarian follicle development in goats
- ALKBH5-mediated m6A demethylation fuels cutaneous wound re-epithelialization by enhancing PELI2 mRNA stability
- Frontiers in Topical Photoprotection
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep