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Research 781–810 of 1000+
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Antimüllerian hormone to determine polycystic ovarian morphology
- Serum anti-Müllerian hormone: A potential biomarker for polycystic ovary syndrome
- Approach to androgen excess in women: Clinical and biochemical insights
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Androgen Levels and Body Size Are Associated with Directional as Well as Fluctuating Asymmetry Patterns in Adult !Kung San and Kavango Males from Northern Namibia
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Epigenetic regulation of 5α reductase-1 underlies adaptive plasticity of reproductive function and pubertal timing
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- The impact of polycystic ovary syndrome on women’s quality of life: Nursing guidelines for its
- Adverse Reactions to Biologic Medications Used in Allergy and Immunology Diseases
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Isolation, Cultivation, and Morphological Characteristics of Hair Follicle Adult Stem Cells in the Bulge Region in Mouse and Human
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Author response: scRNA+TCR-seq reveals the proportion and characteristics of dual TCR Treg cells in mouse lymphoid and non-lymphoid tissues
- Impact of different mating and surgical protocols on the establishment of a mouse model for fetal scarless skin healing
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Solidariedade e plasticidade fenotípica entre indivíduos de Thunbergia grandiflora Roxb. e Russelia equisetiformis Schltdl. & Cham.
- 304 Sephardic Ancestry in Recessive Dystrophic Epidermolysis Bullosa Individuals Carrying the Prevalent c.6527insC Mutation
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Mechanism of Vitamin D Receptor Action
- The keratins and their disorders