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Research 481–510 of 1000+
- Molecular genetics of androgen insensitivity
- Nuclear Factor I-C promotes proliferation and differentiation of apical papilla-derived human stem cells in vitro
- The intragenic mRNA-microRNA regulatory network during telogen-anagen hair follicle transition in the cashmere goat
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- RNA sequence analysis of dermal papilla cells’ regeneration in 3D culture
- Clinical use of 5α-reductase inhibitors
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Tracing the cellular origin of cancer
- Identifying the Target Cells and Mechanisms of Merkel Cell Polyomavirus Infection
- <i>Sept4/</i> ARTS Regulates Stem Cell Apoptosis and Skin Regeneration
- Fibroblast growth factor 5-short (FGF5s) inhibits the activity of FGF5 in primary and secondary hair follicle dermal papilla cells of cashmere goats
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Identification of microRNAs in Wool Follicles during Anagen, Catagen, and Telogen Phases in Tibetan Sheep
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Transcriptomic analysis reveals critical genes for the hair follicle of Inner Mongolia cashmere goat from catagen to telogen
- Identification and characterization of an antisense RNA transcript (gfg) from the human basic fibroblast growth factor gene.
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene on Fibre Traits in Inner Mongolia Cashmere Goats
- Alopecia areata in a rhesus monkey (Macaca mulatta)
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- SlPHL1, a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- LRIG1 is a positive prognostic marker in Merkel cell carcinoma and Merkel cell carcinoma expresses epithelial stem cell markers
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Analyzing the innate immunity of NIH hairless mice and the impact of gut microbial polymorphisms on<i>Listeria monocytogenes</i>infection