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Research 151–180 of 680
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Polycystic ovary syndrome and iron overload: biochemical link and underlying mechanisms with potential novel therapeutic avenues
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Lifestyle Factors Involved in the Pathogenesis of Alopecia Areata
- Exploring the application of dietary antioxidant index for disease risk assessment: a comprehensive review
- The Prevalence of Polycystic Ovary Syndrome, Its Phenotypes and Cardio-Metabolic Features in a Community Sample of Iranian Population: Tehran Lipid and Glucose Study
- The Multi-Faceted Role of Gut Microbiota in Alopecia Areata
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- A Comprehensive Review: The Bidirectional Role of Sebum in Skin Health
- Editorial: Untangle the broad connections and tight interactions between human microbiota and complex diseases through data-driven approaches, volume II
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- An Infant with Worsening Rash
- Post-COVID-19 Syndrome Mechanisms, Prevention and Management
- Evaluation of noninvasive biospecimens for transcriptome studies
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Proopiomelanocortin (POMC) and Psychodermatology
- Prevalence and Levels of Thyroid Autoantibodies in Polycystic Ovary Syndrome—Impact of TSH- and BMI-Matched Comparisons: A Systematic Review and Meta-Analysis