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Research 631–660 of 1000+
- Nuclear Topology, Epigenetics, and Keratinocyte Differentiation
- 14. Wound Healing; Cutaneous Therapy; Hair
- Wound Healing Mechanisms
- Predictive Metagenomic Profiling, Urine Metabolomics, and Human Marker Gene Expression as an Integrated Approach to Study Alopecia Areata
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Inducible, reversible hair loss in transgenic mice.
- Learning from nudity: lessons from the nude phenotype
- Activator Protein-1 Activity Regulates Epithelial Tumor Cell Identity
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- The nude gene and the skin
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Association between DNA Methylation in the Core Promoter Region of the CUT-like Homeobox 1 (CUX1) Gene and Lambskin Pattern in Hu Sheep
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- c-Myc activation in transgenic mouse epidermis results in mobilization of stem cells and differentiation of their progeny
- Apoptosis in human skin development: Morphogenesis, periderm, and stem cells
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- An Update of Congenital Adrenal Hyperplasia
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Activation of Polyamine Catabolism Profoundly Alters Tissue Polyamine Pools and Affects Hair Growth and Female Fertility in Transgenic Mice Overexpressing Spermidine/SpermineN 1-Acetyltransferase
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- Androgens and androgen receptor action in skin and hair follicles
- Melanocytes: The new Black
- Biology and Genetics of Hair
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice