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Research 241–270 of 1000+
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Male-pattern baldness susceptibility locus at 20p11
- Development of Heritable Melanoma in Transgenic Mice
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Molecular genetics of androgen insensitivity
- Congenital Adrenal Hyperplasia
- Molecular Regulation of Melanocyte Senescence
- Physiology of the Hypothalamic Pituitary Gonadal Axis in the Male
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Induction of Hair Growth by Insulin-Like Growth Factor-1 in 1,763 MHz Radiofrequency-Irradiated Hair Follicle Cells
- Toxic shock syndrome: Recent developments in pathogenesis
- Androgenetic Alopecia: In Vivo Models
- Artificial skin for wound healing
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA
- Penis Endocrinology
- Transforming growth factor-β in stem cells and tissue homeostasis
- Effects of Short-Term Finasteride on Apoptotic Factors and Androgen Receptors in Prostate Cancer Cells
- Activation of the OVOL1-OVOL2 Axis in the Hair Bulb and in Pilomatricoma
- 46, XY Disorder of Sexual Development with Ambiguous Female External Genitalia: A Case Report
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- THE PATHOGENESIS OF ALOPECIA AREATA
- What causes hidradenitis suppurativa ?—15 years after
- The hair shaft: normality, abnormality, and genetics
- IV Międzynarodowe Sympozjum Studenckich Kół Naukowych Środowisko – Roślina – Zwierzę – Produkt Streszczenia
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Do Changes in Chromosomes Cause Aging?