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Research 391–420 of 1000+
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- ATP-dependent chromatin remodeling during mammalian development
- Cutaneous signs in COVID ‐19 patients: A review
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- Alopecia areata
- Function and underlying mechanisms of seasonal colour moulting in mammals and birds: what keeps them changing in a warming world?
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Androgen receptors and their biology
- Compartmentalized organization: a common and required feature of stem cell niches?
- Alopecia areata update
- Gender aspects in skin diseases
- Roles of tumor suppressors in regulating tumor-associated inflammation
- Cicatricial (Scarring) Alopecias
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- What does acne genetics teach us about disease pathogenesis?
- Skin disease in pregnancy
- Overexpression of IL-18 in the Proliferative Phase Endometrium of Patients With Polycystic Ovary Syndrome
- Genetic basis of polycystic ovary syndrome
- Skin diseases in consequence of endocrine alterations
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- Alcohol Exposure During Late Adolescence Increases Drinking in Adult Wistar Rats, an Effect that is not Reduced by Finasteride
- Increased 25(OH)D3 level in redheaded people: Could redheadedness be an adaptation to temperate climate?
- Function of KLF4 in Stem Cell Biology
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Causal Relationship Between Sleep Characteristics and Alopecia Areata and Other Non-Scarring Alopecia: A Two-Sample Bidirectional Mendelian Randomization Analysis
- Melanocytes and Vitiligo (and Hair Graying)
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring