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Research 511–540 of 1000+
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Physiological Regeneration of Skin Appendages and Implications for Regenerative Medicine
- The sequence of lanugo pattern development on the trunk wall in human fetuses
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- Integrin signalling regulates YAP/TAZ to control skin homeostasis
- Matriptase: Potent Proteolysis on the Cell Surface
- Extra-Intestinal Manifestation of Celiac Disease in Children
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- Does Vitamin D play a role on Msx1 homeoprotein expression involving an endogenous antisense mRNA?*1
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Temperature‐sensitive hydrogel releasing pectolinarin facilitate scarless wound healing
- Defining the impact of β-catenin/Tcf transactivation on epithelial stem cells
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Mesenchymal Stromal Cell-Conditioned Medium for Skin Diseases: A Systematic Review
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Premature aging and cancer development in transgenic mice lacking functional CYLD
- Ligand‐Independent Actions of the Vitamin D Receptor: More Questions Than Answers
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Overexpression of Smad7 results in severe pathological alterations in multiple epithelial tissues
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- Lean Women with Polycystic Ovary Syndrome
- H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers
- The transcription elongation factors Spt4 and Spt6 promote dermal adipocyte differentiation