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Research 331–360 of 1000+
- Cell Type-specific Functions of the Lysosomal Protease Cathepsin L in the Heart
- 46,XY DSD due to impaired androgen production
- In Vitro Differences Between Keratinocyte Stem Cells and Transit-Amplifying Cells of the Human Hair Follicle
- The prevalence of idiopathic hirsutism and polycystic ovary syndrome in the Tehran Lipid and Glucose Study
- JunB defines functional and structural integrity of the epidermo-pilosebaceous unit in the skin
- Long COVID: Clinical characteristics, proposed pathogenesis and potential therapeutic targets
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- LHX2 is a direct NF-κB target gene that promotes primary hair follicle placode down-growth
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Comparison of clinical and laboratory characteristics of cases with polycystic ovarian syndrome based on Rotterdam’s criteria and women whose only clinical signs are oligo/anovulation or hirsutism
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Understanding the role of prostaglandin E2 in regulating human platelet activity in health and disease
- Targeted expression of activated erbB-2 to the epidermis of transgenic mice elicits striking developmental abnormalities in the epidermis and hair follicles.
- Polycystic Ovarian Syndrome: Long-Term Health Consequences
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Epigen Transgenic Mice Develop Enlarged Sebaceous Glands
- The Frequency of Metabolic Syndrome is Higher Among PCOS Brazilian Women With Menstrual Irregularity Plus Hyperandrogenism
- Systemic Lupus Erythematosus: Definitions, Contexts, Conflicts, Enigmas
- <i>WNT10A</i> , dermatology and dentistry
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- A rational approach to the diagnosis of polycystic ovarian syndrome during adolescence
- Esrp1-Regulated Splicing of Arhgef11 Isoforms Is Required for Epithelial Tight Junction Integrity
- Lipid droplets and associated proteins in sebocytes
- Immunodeficiency Disorders
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Keratins: the hair shaft's backbone revealed
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- PCOS: update and diagnostic approach
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Prevalence and characteristics of polycystic ovary syndrome in Brazilian women: protocol for a nation-wide case–control study