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Research 541–570 of 1000+
- Androgenetic Alopecia: A Review
- The Hormonal Background of Hair Loss in Non-Scarring Alopecias
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Significance of stress keratin expression in normal and diseased epithelia
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Hox genes in development and beyond
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Exploring the role of stem cells in cutaneous wound healing
- ENZYMES
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- Prevalence of polycystic ovary syndrome under NIH criteria among the tenth-grade Chinese schoolgirls in Guangzhou area: a cross-sectional epidemiological survey
- Melanocytes in regenerative medicine applications and disease modeling
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Main Plenary Sessions: Summaries of Papers
- Morphological Approach to Hair Disorders
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Expression patterns of MITF during human cutaneous embryogenesis: evidence for bulge epithelial expression and persistence of dermal melanoblasts
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- Interleukin-1 Induces Transcription of Keratin K6 in Human Epidermal Keratinocytes
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Evidence of Heterogeneity and Quantitative Differences of the Type 1 5α-Reductase Expression in Cultured Human Skin Cells – Evidence of its Presence in Melanocytes
- Women's Dermatologic Diseases, Health Care Delivery, and Socioeconomic Barriers
- Surgical approach of ectropion in lamellar ichthyosis
- Ischemic onycholysis of the hands