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Research 421–450 of 1000+
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Hirsutism in the Adolescent Female
- Alopecia Areata, Primary Sclerosing Cholangitis, and Ulcerative Colitis: Autoimmunity and Apoptosis as Common Links?
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Big head? Bald head! Skull expansion: alternative model for the primary mechanism of AGA
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Differential impact of environmental factors on systemic and localized autoimmunity
- Predicting Human Appearance from DNA for Forensic Investigations
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- Causal Relationship Between Sleep Characteristics and Alopecia Areata and Other Non-Scarring Alopecia: A Two-Sample Bidirectional Mendelian Randomization Analysis
- The G1/S transition in mammalian stem cells in vivo is autonomously regulated by cell size
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Expression and Distribution of the Guanine Nucleotide-binding Protein Subunit Alpha-s in Mice Skin Tissues and Its Association with White and Black Coat Colors
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Aged differentiated cells reverse into native stemness-like state by niche cytokines to sustain lifelong homeostasis and tissue repair
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Concomitant acute alopecia and profound bone marrow suppression: An unusual manifestation of azathioprine toxicity
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- THE MULTIFACETED APPROACH TO POLYCYSTIC OVARIAN SYNDROME: A REVIEW OF TRADITIONAL AND ALLOPATHIC MEDICINE
- Deletion of adipocyte Sine Oculis Homeobox Homolog 1 prevents lipolysis and attenuates skin fibrosis
- Factors associated with early-onset androgenetic alopecia: A scoping review
- Androgen excess: a hallmark of polycystic ovary syndrome
- Fertility and Sterility Vol 101 No 4, April 2014
- Dermatological manifestations associated with pregnancy