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Research 541–570 of 1000+
- 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
- Ether: Fiction or Reality? A Review
- Prevalence Of Male Balding Pattern In Patient From Saveetha Dental College- Retrospective Comparative Evaluation Study
- 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> )
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- 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
- Nonclassic adrenal hyperplasia
- Animal Models and the Developmental Origins of Polycystic Ovary Syndrome: Increasing Evidence for the Role of Androgens in Programming Reproductive and Metabolic Dysfunction
- 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.
- 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
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Biology of Human Hair: Know Your Hair to Control It
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Role of skin enzymes in metabolism of topical drugs
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Sprayable supramolecular hydrogel with minimalism for wilderness first aid: integration of mechanical performance and biofunctionality
- 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
- Identification and expression of the target gene SLC24A2 of oar-miR-377 and its novel SNPs effects on wool traits in sheep
- Fertility and Sterility Vol 101 No 4, April 2014
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations