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Research 391–420 of 1000+
- Large-Scale, Multicenter, Prospective Registry Study of Ripretinib in Advanced GIST: A Real-World Study from China
- Zebrafish Model of Hereditary Pigmentary Disorders
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- COVID-19: How Effective Are the Repurposed Drugs and Novel Agents in Treating the Infection?
- Congenital Adrenal Hyperplasia
- Efficacy and safety of the Exfoliate-Dissolve-Repair skin care approach in the treatment of keratosis pilaris: a randomized controlled clinical trial study protocol
- Genetics of Alopecia
- Le mélanome malin bilatéral de l'uvée
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Vitamina D y la piel. Una revisión para dermatólogos
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Carcinogenesis of the Human Scalp. An Immunometabolic Centered View
- The role of medicinal plants in the treatment of Coronavirus infections
- 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Acne Syndromes and Mosaicism
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- WNT Signaling in Disease
- Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Amino acid–derived defense metabolites from plants: A potential source to facilitate novel antimicrobial development
- Genetics of Inherited Ichthyoses and Related Diseases
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Clinical biochemistry of dihydrotestosterone