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Research 61–90 of 1000+
- Cellular heterogeneity and microenvironmental control of skin cancer
- Frizzled Receptors in Development and Disease
- Impaired Lef1 activation accelerates iPSC-derived keratinocytes differentiation in Hutchinson-Gilford Progeria Syndrome
- Central Centrifugal Cicatricial Alopecia Associated With PDL1 Loss and Increased Expression of Caspase 3: A Case Series
- Exact, time-independent estimation of clone size distributions in normal and mutated cells
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Beyond Wavy Hairs
- The interplay of oxidative stress and immune dysfunction in Hashimoto’s thyroiditis and polycystic ovary syndrome: a comprehensive review
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- KIF18B is a cell-type specific regulator of spindle orientation in the epidermis
- Primary Generalized Glucocorticoid Resistance and Hypersensitivity
- The Endocrine Function of the Skin: An Analytical Narrative
- Developmental Genetics of Color Pattern Establishment in Cats
- Rand Protease: The Role of Calcium-Binding Site on Stability with Mutagenesis and The Effectiveness on Leather Dehairing
- Human hair melanins: what we have learned and have not learned from mouse coat color pigmentation
- Human hair melanins: what we have learned and have not learned from mouse coat color pigmentation
- Generalised Glucocorticoid Resistance
- Tracing the cellular origin of cancer
- Homeostatic maintenance of the murine corneal epithelium in pathophysiological contexts
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- The ITGB6 gene: its role in experimental and clinical biology
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- Le gène<i>hairless</i>de la souris
- Hutchinson-gilford progeria syndrome and its relevance to cardiovascular diseases and normal aging.
- Cystatin M/E Is a High Affinity Inhibitor of Cathepsin V and Cathepsin L by a Reactive Site That Is Distinct from the Legumain-binding Site