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Research 31–60 of 1000+
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Natural phenylethanoid glycoside forsythoside A alleviates androgenetic alopecia by selectively inhibiting TRPV3 channels in mice
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- The nude gene and the skin
- <i>Hoxc13</i> mutant mice lack external hair
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Quantitative Models for the Study of Hair Growth <i>in Vivo</i><sup>a</sup>
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- A missense mutation in Lama3 causes androgen alopecia
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- The origins of skin diversity: lessons from dermal fibroblasts
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- Morphogenetic Mechanisms in the Cyclic Regeneration of Hair Follicles and Deer Antlers from Stem Cells
- Integrated analysis of miRNAs and mRNA profiling reveals the potential roles of miRNAs in sheep hair follicle development
- Hair Follicle Transcriptome Analysis Reveals Differentially Expressed Genes That Regulate Wool Fiber Diameter in Angora Rabbits
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Possible Integrative Approaches to Treatment of Alopecia: A Case Study Provides a Protocol Approach
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Hair Loss in Women
- Critical Stages of Hair Development and Pigmentation in the Mouse
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Towards Defining the Pathogenesis of the Hairless Phenotype
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Effect of UV Radiation on Scalp and Hair Growth
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Ex vivo detection of SARS CoV 2 spike protein in human hair follicles and potential link to telogen effluvium
- miR-29a-5p Inhibits Prenatal Hair Placode Formation Through Targeting EDAR by ceRNA Regulatory Network