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Research 241–270 of 1000+
- Functional Enhancers As Master Regulators of Tissue-Specific Gene Regulation and Cancer Development.
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- B-Raf and C-Raf Are Required for Melanocyte Stem Cell Self-Maintenance
- Activation of AR Sensitizes Breast Carcinomas to NVP-BEZ235's Therapeutic Effect Mediated by PTEN and KLLN Upregulation
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Bioarchitectural Design of Bioactive Biopolymers: Structure–Function Paradigm for Diabetic Wound Healing
- NEONATAL INHIBITION OF ANDROGEN ACTIVITY ALTERS THE PROGRAMMING OF BODY WEIGHT AND OREXINERGIC PEPTIDES DIFFERENTIALLY IN MALE AND FEMALE RATS
- Editor's evaluation: Role of distinct fibroblast lineages and immune cells in dermal repair following UV radiation-induced tissue damage
- Epithelial-Mesenchymal Micro-niches Govern Stem Cell Lineage Choices
- Regulation of adult stem cell quiescence and its functions in the maintenance of tissue integrity
- Resting no more: re‐defining telogen, the maintenance stage of the hair growth cycle
- The structure and organization of lanceolate mechanosensory complexes at mouse hair follicles
- Coactivator MED1 Ablation in Keratinocytes Results in Hair-Cycling Defects and Epidermal Alterations
- WNT Signaling in Disease
- 9. Immunology and Genetics
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Do Changes in Chromosomes Cause Aging?
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Insertional mutation of the hairless locus on mouse Chromosome 14