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Research 601–630 of 1000+
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Pharmacologic interventions in aging hair
- Aging of the hair follicle pigmentation system
- Milestones in Photocarcinogenesis
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Expression profile of long non-coding RNA in inner Mongolian cashmere goat with putative roles in hair follicles development
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Pathological Skin Scarring: From Mechanism to Targeted Local Therapy
- Technological Advances in Anti-hair Loss and Hair Regrowth Cosmeceuticals: Mechanistic Breakthroughs and Industrial Prospects Driven by Multidisciplinary Collaborative Innovation
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- The Genomic Variation in Textured Hair: Implications in Developing a Holistic Hair Care Routine
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Acne Vulgaris
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Viewpoint 2
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Creatine phosphokinase levels and isotretinoin therapy
- Health Utility of Facial Angiofibroma associated with Tuberous Sclerosis Complex
- Hormonal Control of Cardiac Action Potential Phase 1 Currents in the Brugada Syndrome
- SELF-CARE OF MALE PATTERN HAIR LOSS – Selfcare Journal
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Surgical approach of ectropion in lamellar ichthyosis
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Evaluation of Hair Loss
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation