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Research 781–810 of 1000+
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- Le gène<i>hairless</i>de la souris
- FINASTERIDE INHIBITS 5?-REDUCTASE ACTIVITY IN HUMAN DERMAL FIBROBLASTS: PREDICTION OF ITS THERAPEUTIC APPLICATION IN ANDROGEN-RELATED SKIN DISEASES
- Virilizing insulinoma
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Nucleic acid-induced chemokine expression in keratinocytes: Implications for skin inflammation
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Regulation of masculinization: androgen signalling for external genitalia development
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- YAP1 promotes adipogenesis by regulating the negative feedback mechanism of the Hippo signaling pathway via LATS2
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Stem Cells and their Niches
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Seasonal Gene Expression Profile Responsible for Hair Follicle Development in Angora Goats
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Dicer- and BSC-dependent miRNAs during murine anagen development
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Alopecia areata in a rhesus monkey (Macaca mulatta)
- Cardiac biopsy in myocarditis
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- WNT10B (wingless-type MMTV integration site family)
- Interrelation of immunity and tissue repair or regeneration