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Research 751–780 of 1000+
- Management Approaches to Congenital Adrenal Hyperplasia in Adolescents and Adults; Latest Therapeutic Developments
- The genetic evolution of skin squamous cell carcinoma: tumor suppressor identity matters
- Pseudo Pemphigus Phenotypes in Mice with Inactivated Desmoglein 3
- [Genetic expression and morphogenesis of the skin in vertebrates].
- Le gène<i>hairless</i>de la souris
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI)
- Steatocystoma Multiplex
- Human Regulatory T Cells: Understanding the Role of Tregs in Select Autoimmune Skin Diseases and Post-Transplant Nonmelanoma Skin Cancers
- [Anejaculation caused by haemosiderosis: male infertility in hereditary haemochromatosis].
- LB1031 Immune Cell-Mediated Amplification of Stem Cell Activation in Hairy Melanocytic Nevus via Osteopontin-CD44 Axis
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- Inherited Acrodermatitis Enteropathica
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Pilomatricoma in the infraorbital region
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- Loose anagen syndrome in one identical twin girl.
- Dumhetens rum i bildningens mitt
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- [Molecular cloning of full-long cDNA sequences encoding hairless gene in the Kunming mouse].
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- ALX4-related frontonasal dysplasia sequence presenting with alopecia in a 12 year old girl
- 1322 A non-cell autonomous dermal hedgehog signaling mechanism for follicular neoplasia and induction
- The Tumor Suppressor Actions of the Vitamin D Receptor in Skin
- In the quest to stymie time, will laboratory data stand up in man?
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation