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Research 391–420 of 1000+
- Alopecia in Epidermolysis Bullosa
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- The dermatological consequences of obesity
- Epimorphic regeneration in mice is p53-independent
- Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene on Fibre Traits in Inner Mongolia Cashmere Goats
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Relating neurosteroid modulation of inhibitory neurotransmission to behaviour
- Genetic basis of polycystic ovary syndrome
- Expression patterns of the glial cell line–derived neurotrophic factor, neurturin, their cognate receptors GFRα-1, GFRα-2, and a common signal transduction element c-Ret in the human skin hair follicles
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Regeneration of Hair Follicles Is Modulated by Flightless I (Flii) in a Rodent Vibrissa Model
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Androgen Receptor Actions Modify Skin Structure and Chemical Carcinogen-induced Skin Cancer Susceptibility in Mice
- Targeted expression of SV40 T antigen in the hair follicle of transgenic mice produces an aberrant hair phenotype
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Pannexin 3 regulates skin development via Epiprofin
- Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency
- Cytoskeletal Regulation of Dermal Regeneration
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Dermatopathology and molecular genetics
- SlPHL1, a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response
- Lineage Tracing of Hair Follicle Stem Cells in Epidermal Whole Mounts
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma