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Research 841–870 of 1000+
- Alopecia: evaluation and treatment
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Exploring the new horizons of drug repurposing: A vital tool for turning hard work into smart work
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Epidermal Nevi
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- Significance of the polyglutamine tract polymorphism in the androgen receptor
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Characteristics of Androgenetic Alopecia in Asian
- Do Changes in Chromosomes Cause Aging?
- Current Advanced Therapies Based on Human Mesenchymal Stem Cells for Skin Diseases
- A Comparison of the Hormonal Profile of Early Androgenetic Alopecia in Men With the Phenotypic Equivalent of Polycystic Ovarian Syndrome in Women
- The Pharmacology of Regenerative Medicine
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Pathomechanisms of immune-mediated alopecia
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Recently Identified Forms of Epidermolysis Bullosa