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Research 181–210 of 1000+
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Toll-like receptor-targeted anti-tumor therapies: Advances and challenges
- Myotonic Dystrophy—A Progeroid Disease?
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Identification of the Ovine Keratin-Associated Protein 26-1 Gene and Its Association with Variation in Wool Traits
- Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- Cornu cervi pantotrichum Pharmacopuncture Solution Facilitate Hair Growth in C57BL/6 Mice
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Design of Liposome Formulations for CRISPR/Cas9 Enzyme Immobilization: Evaluation of 5-Alpha-Reductase Enzyme Knockout for Androgenic Disorders
- Ovine KRTAP36-2: A New Keratin-Associated Protein Gene Related to Variation in Wool Yield
- Androgenetic alopecia: a review
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Differential expression of steroid 5α-reductase isozymes and association with disease severity and angiogenic genes predict their biological role in prostate cancer
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Predicting Physical Appearance from Low Template: State of the Art and Future Perspectives
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Comprehensive transcriptome profiling between balding and non-balding scalp of female pattern hair loss in Asian
- Barley disease susceptibility factor RACB acts in epidermal cell polarity and positioning of the nucleus
- Autoantigen Discovery in the Hair Loss Disorder, Alopecia Areata: Implication of Post-Translational Modifications
- Recent Advances in Genome-Editing Technology with CRISPR/Cas9 Variants and Stimuli-Responsive Targeting Approaches within Tumor Cells: A Future Perspective of Cancer Management
- Industry updates in advanced therapy medicinal products and regenerative medicine – March 2026
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis