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Research 931–960 of 1000+
- Molecular Regulation of Melanocyte Senescence
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Effects of 5-alpha reductase inhibitors on erectile function, sexual desire and ejaculation
- From neural crest cells to melanocytes: cellular plasticity during development and beyond
- The Role of Micronutrients in Alopecia Areata: A Review
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Zinc as an ambivalent but potent modulator of murine hair growth in vivo- preliminary observations
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- 46,XY DSD due to impaired androgen production
- Prolactin delays hair regrowth in mice
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Wnt signaling: the good and the bad
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- 5α-Reduced glucocorticoids: a story of natural selection
- Combined hormonal contraception and venous thromboembolism
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Androgen receptor gene CAG repeat polymorphism in women with polycystic ovary syndrome
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hair loss disorders: Rare, but not too rare
- Realising the therapeutic potential of neuroactive steroid modulators of the GABAA receptor