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Research 571–600 of 1000+
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Skin and hair: models for exploring organ regeneration
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Androgenetic alopecia: pathogenesis and potential for therapy
- Nitroxide pharmaceutical development for age-related degeneration and disease
- Association between Polymorphisms of OCT1 and Metabolic Response to Metformin in Women with Polycystic Ovary Syndrome
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Comprehensive Analysis of LncRNA AC010789.1 Delays Androgenic Alopecia Progression by Targeting MicroRNA-21 and the Wnt/β-Catenin Signaling Pathway in Hair Follicle Stem Cells
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Molecular Mechanisms Affecting Development of Animal Fibers and Some Studies on Goats
- Molecular mechanisms of androgenetic alopecia
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Induction of cardiomyocyte‑like cells from hair follicle cells in mice
- Liposome-Based Carriers for CRISPR Genome Editing
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Genetic prediction of male pattern baldness
- Molecular pathology of skin adnexal tumours
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Molecular and Pathological Studies on Sarcoptes scabiei in Sheep in Ismailia Province, Egypt.
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- The keratins and their disorders
- New small molecules in dermatology: for the autoimmunity, inflammation and beyond
- Molecular Signaling and Nutritional Regulation in the Context of Poultry Feather Growth and Regeneration