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Research 601–630 of 1000+
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- Progress in Research and Prospects for Application of Precision Gene-Editing Technology Based on CRISPR–Cas9 in the Genetic Improvement of Sheep and Goats
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Biomedical engineering approaches for the delivery of JAGGED1 as a potential tissue regenerative therapy
- Overview of the Circadian Clock in the Hair Follicle Cycle
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- ATP-dependent chromatin remodeling during mammalian development
- Design of Liposome Formulations for CRISPR/Cas9 Enzyme Immobilization: Evaluation of 5-Alpha-Reductase Enzyme Knockout for Androgenic Disorders
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- New aspects of vitamin D metabolism and action — addressing the skin as source and target
- Spermidine/spermine-<i>N</i><sup>1</sup>-acetyltransferase: a key metabolic regulator
- Splitting Hairs
- Dermal fibroblast in cutaneous development and healing
- Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Fidelity of the Human Mitochondrial DNA Polymerase
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Molecular Regulation of Melanocyte Senescence
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Understanding autoimmunity of vitiligo and alopecia areata
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- 5α-Reduced glucocorticoids: a story of natural selection
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Regeneration Genetics
- Recently Identified Forms of Epidermolysis Bullosa
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome