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Research 931–960 of 1000+
- Reshaped DNA methylation cooperating with homoeolog‐divergent expression promotes improved root traits in synthesized tetraploid wheat
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- POLİKİSTİK OVER SENDROMU'NUN ALT GRUPLARINDA METABOLİK ÖZELLİKLER
- British Society for Paediatric Dermatology Annual Meeting, Sheffield, 18-19 November 2016
- Author response: ETS family transcriptional regulators drive chromatin dynamics and malignancy in squamous cell carcinomas
- Effect of ethnicity on the clinical presentations of women with polycystic ovary syndrome: a 20-year retrospective cohort study
- The polycystic ovary syndrome: a position statement from the European Society of Endocrinology
- Neurotrophins, nociceptors, and pain
- Mechanical stretch induces hair regeneration through the alternative activation of macrophages
- Functional histopathology of keloid disease.
- Deficiency of kinase suppressor of Ras1 prevents oncogenic ras signaling in mice.
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Polycystic Ovary Syndrome
- The Senescence–Stemness Alliance – A Cancer-Hijacked Regeneration Principle
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia
- Targeting lymphoid-derived IL-17 signaling to delay skin aging
- WNT5A drives interleukin-6-dependent epithelial–mesenchymal transition via the JAK/STAT pathway in keloid pathogenesis
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits
- Physical inactivity is a disease synonymous for a non-permissive brain disorder
- Assessment of anogenital distance as a diagnostic tool in polycystic ovary syndrome
- Clinical characteristics in Taiwanese women with polycystic ovary syndrome
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- Electrophoretic variability in human head hair: Polyacrylamide gel electrophoresis of hair proteins in the presence of sodium dodecyl sulfate and urea
- N6-methyladenosine RNA Methylation Correlates with Immune Microenvironment and Immunotherapy Response of Melanoma
- Tissue Mechanics in Haired Murine Skin: Potential Implications for Skin Aging