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Research 31–60 of 247
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Androgens and androgen receptor action in skin and hair follicles
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Wnt Signaling in Skin Development, Homeostasis, and Disease
- Decreased Serum Ferritin is Associated With Alopecia in Women
- Hierarchical patterning modes orchestrate hair follicle morphogenesis
- The disintegrin/metalloproteinase Adam10 is essential for epidermal integrity and Notch-mediated signaling
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Wnt and Notch signaling pathway involved in wound healing by targeting c-Myc and Hes1 separately
- Targeting the Wnt pathways for therapies
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Molecular Regulation of Melanocyte Senescence
- Bacteria induce skin regeneration via IL-1β signaling
- 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
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice
- 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
- Mechanisms and cell lineages in lymphatic vascular development
- A Mouse Model of Androgenetic Alopecia
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Acquired scalp alopecia. Part II: A review
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Polyamines and hair: a couple in search of perfection