Search
for
Sort by
Research 421–450 of 1000+
- Functional Ingredient Mapping in PCOS Formulations: Hormonal Excess
- Polycystic ovary syndrome
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Role of skin enzymes in metabolism of topical drugs
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- THE MULTIFACETED APPROACH TO POLYCYSTIC OVARIAN SYNDROME: A REVIEW OF TRADITIONAL AND ALLOPATHIC MEDICINE
- Traditional and Integrative Approaches to the Treatment of Alopecia
- CPC12 Coinheritance of <i>BRCA2</i> and <i>CYLD</i> germline pathogenic variants associated with targetable metastatic malignant cylindroma
- Fertility and Sterility Vol 101 No 4, April 2014
- Symposium Proceedings of the 4th Intercontinental Meeting of Hair Research Societies: “The World of Hair 2004”
- Can UK undergraduate dental programmes provide training in non-surgical facial aesthetics?
- PENYULUHAN DAN PELATIHAN PEMBUATAN MASKER RAMBUT DAUN PEPPERMINT DI DESA CIBIRU WETAN KABUPATEN BANDUNG
- “Formulation and Evaluation of Polyherbal Hair Serum
- 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
- Biology of Human Hair: Know Your Hair to Control It
- Ethno-medico-botanical claims of Bondla wildlife sanctuary vicinity of Goa
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Androgen receptor gene polymorphism and biological age markers in men
- Hashimoto Thyroiditis - A Comprehensive Review
- Becker nevus of the face with asymmetrical growth of beard hair
- British Society for Dermatopathology
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique