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Research 271–300 of 1000+
- Alopezien und Hypotrichosen im Kindesalter
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development
- Marie-unna hereditary hypotrichosis
- Prunus mira Koehne in Sichuan, China: Recorded History as a Medicine and Food, Modern Applications, Distribution, and Ethnobotanical Investigations
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Evaluation of Susceptibility Genes/Loci Associated with Male Androgenetic Alopecia (MAGA) for Female-Pattern Hair Loss in a Chinese Han Population and a Brief Literature Review
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Obesity in Adults: Position Statement of Polish Association for the Study on Obesity, Polish Association of Endocrinology, Polish Association of Cardiodiabetology, Polish Psychiatric Association, Section of Metabolic and Bariatric Surgery of the Association of Polish Surgeons, and the College of Family Physicians in Poland
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- An updated landscape of Female Pattern Hair Loss
- Androgenetic Alopecia in Polycystic Ovary Syndrome: A Cutaneous Marker of Systemic Metabo-inflammatory and Endocrine Dysfunction: A Narrative Review
- Immortality Reconsidered: Clinical Challenges at the Frontier of Plastic Surgery
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Differences in Demographic and Clinical Characteristics Among Subtypes of Female Pattern Hair Loss
- Monilethrix – Case report of a rare disease
- Pathological Skin Scarring: From Mechanism to Targeted Local Therapy
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- The Genomic Variation in Textured Hair: Implications in Developing a Holistic Hair Care Routine
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness