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Research 601–630 of 1000+
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Analysis of the human diseasome using phenotype similarity between common, genetic and infectious diseases
- Extracellular Vesicles as Surrogates for Drug Metabolism and Clearance: Promise vs. Reality
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Acne Syndromes and Mosaicism
- Clinical Profile of Patchy Alopecia: Report from a Tertiary Care Hospital of Bangladesh
- Review of Different DNA Extraction Methods in Hair Shafts
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Society for Endocrinology guidelines for testosterone replacement therapy in male hypogonadism
- ACE2 and TMPRSS2 Potential Involvement in Genetic Susceptibility to SARS-COV-2 in Cancer Patients
- Bone vs. fat: Embryonic origin of progenitors determines response to androgen in adipocytes and osteoblasts
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- Flavonoids and Nod Factors: Importance in Legume-Microbe Interactions and Legume Improvement
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Characterisation of the Ovine KRTAP36-1 Gene in Chinese Tan Lambs and Its Impact on Selected Wool Traits
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Utilising SNP Association Analysis as a Prospective Approach for Personalising Androgenetic Alopecia Treatment
- Alopecia universalis following human papillomavirus vaccine administration: a case report
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Integrative skin phenotypic and transcriptomic analyses reveal candidate genes for coat color and fiber length in four Chinese goat breeds (<i>Capra hircus</i>)
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix