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Research 391–420 of 1000+
- Vellus-to-terminal Hair Follicle Reconversion Occurs in Male Pattern Balding and is Promoted by Minoxidil and Platelet-rich Plasma: In Vivo Evidence from a New Humanized Mouse Model of Androgenetic Alopecia
- Factors Driving Unique Urination Phenotypes of Male and Female 9-week-old C57BL/6J Mice
- Medical Management Options for Hair Loss
- Single–Follicular-Unit Hair Transplantation to Correct Cleft Lip Moustache Alopecia
- Single–Follicular-Unit Hair Transplantation to Correct Cleft Lip Moustache Alopecia
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Alopecia Areata
- Stem Cells and the Niche: A Dynamic Duo
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- THE PATHOGENESIS OF ALOPECIA AREATA
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- What causes hidradenitis suppurativa ?—15 years after
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- MENSTRUAL DISORDERS IN ADOLESCENTS
- New clinico‐genetic classification of trichothiodystrophy
- Genetics of Inherited Ichthyoses and Related Diseases
- Hair Follicle: A Novel Source of Multipotent Stem Cells for Tissue Engineering and Regenerative Medicine
- An Overview of Alopecias
- How to diagnose a lipodystrophy syndrome
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Genetic Basis of Alopecia Areata
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations