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Research 421–450 of 1000+
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- TRP Channels in Skin Biology and Pathophysiology
- Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer
- Nitrate‐inducible NIGT1 proteins modulate phosphate uptake and starvation signalling via transcriptional regulation of <i>SPX</i> genes
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- The RpoS Gatekeeper in Borrelia burgdorferi: An Invariant Regulatory Scheme That Promotes Spirochete Persistence in Reservoir Hosts and Niche Diversity
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Androgenetic alopecia: An update
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- Generalized Vitiligo Associated Autoimmune Diseases in Japanese Patients Their Families
- The molecular basis of human keratin disorders
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Critical Analysis on Characterization, Systemic Effect, and Therapeutic Potential of Beta-Sitosterol: A Plant-Derived Orphan Phytosterol
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Protein Microarrays
- Exploring Acne Treatments: From Pathophysiological Mechanisms to Emerging Therapies
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp
- Frontiers in alopecia areata pathobiology research
- Regulation of stem cell function by protein ubiquitylation
- Coronavirus 2019 Infectious Disease Epidemic: Where We Are, What Can Be Done and Hope For
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- High-throughput T cell receptor sequencing identifies clonally expanded CD8+ T cell populations in alopecia areata
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Control by a hair’s breadth: the role of microRNAs in the skin
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Race and Alopecia Areata amongst US Women