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Research 421–450 of 1000+
- Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models
- Multiomics global landscape of stemness-related gene clusters in adipose-derived mesenchymal stem cells
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Molecular Mechanisms and Targeted Therapeutics in Androgenetic Alopecia: From Signaling Pathways to Regenerative Approaches
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- The heme-responsive PrrH sRNA regulates <i>Pseudomonas aeruginosa</i> pyochelin gene expression
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- 651 Epigenetic regulation of macrophage activity by glutamine during wound healing
- The necessity of investigations to clarify sex and racial disparities in pathophysiology of Long COVID
- Genome Wide Differential Expression Profiles in Nevus Sebaceous Uncovered Low Expression of CDKN2AIP and Construction of a ceRNA Network
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.