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Research 301–330 of 1000+
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Transcriptomic landscape of early hair follicle and epidermal development
- The heme-responsive PrrH sRNA regulates<i>Pseudomonas aeruginosa</i>pyochelin gene expression
- Phenotypic effect of growth media on <i>Arabidopsis thaliana</i> root hair growth
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Ku80 as a Novel Receptor for Thymosin β4 That Mediates Its Intracellular Activity Different from G-actin Sequestering
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Regeneration of fat cells from myofibroblasts during wound healing
- Neutrophil extracellular traps impair regeneration
- How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Advances in single-cell transcriptomics in animal research
- Developmental genetics of color pattern establishment in cats
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- New frontiers in CRISPR/Cas9 delivery systems delivery for gene editing
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- FGF Family: From Drug Development to Clinical Application
- Elevated Circulation Levels of an Antiangiogenic SERPIN in Patients with Diabetic Microvascular Complications Impair Wound Healing through Suppression of Wnt Signaling
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- miR-140-5p in Small Extracellular Vesicles From Human Papilla Cells Stimulates Hair Growth by Promoting Proliferation of Outer Root Sheath and Hair Matrix Cells
- Disease Prevention and Alleviation by Human Myoblast Transplantation
- Skin regional specification and higher-order <i>HoxC</i> regulation