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Research 571–600 of 1000+
- Using the Web as a Resource on Hair Loss
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Transcriptomic inspection revealed a possible pathway regulating the formation of the high-quality brush hair in Chinese Haimen goat ( <i>Capra hircus</i> )
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Red ginseng monograph
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Association between genetically predicted rheumatoid arthritis and alopecia areata: a two-sample Mendelian randomization study
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- The voices of adult offspring of sperm donation: forces for change within assisted reproductive technology in the United States
- Ether: Fiction or Reality? A Review
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- 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
- Induction of dermal fibroblasts into dermal papilla cell-like cells in hydrogel microcapsules for enhanced hair follicle regeneration
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Exploring the Lived Experiences and Coping Mechanisms of Unmarried Women with Polycystic Ovary Syndrome (PCOS) in Pakistan
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy