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Research 541–570 of 1000+
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Transcriptomic inspection revealed a possible pathway regulating the formation of the high-quality brush hair in Chinese Haimen goat ( <i>Capra hircus</i> )
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Pregnancy in postpartum estrus induces inflammatory milk production and catagen specific pup skin inflammation in interleukin-10 deficient mice
- Association between genetically predicted rheumatoid arthritis and alopecia areata: a two-sample Mendelian randomization study
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Ether: Fiction or Reality? A Review
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Traditional and Integrative Approaches to the Treatment of Alopecia
- Prevalence Of Male Balding Pattern In Patient From Saveetha Dental College- Retrospective Comparative Evaluation Study
- Nonclassic adrenal hyperplasia
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- THE MULTIFACETED APPROACH TO POLYCYSTIC OVARIAN SYNDROME: A REVIEW OF TRADITIONAL AND ALLOPATHIC MEDICINE
- Hair loss in children.
- Androgen receptor gene polymorphism and biological age markers in men
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Hair and nail involvement in lupus erythematosus
- Biology of Human Hair: Know Your Hair to Control It
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Role of skin enzymes in metabolism of topical drugs
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Enhanced Insights into Frontal Fibrosing Alopecia: Advancements in Pathogenesis Understanding and Management Strategies