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Research 481–510 of 1000+
- Transcriptome Analysis of Improved Wool Production in Skin-Specific Transgenic Sheep Overexpressing Ovine β-Catenin
- Glucocorticoid and Sex Hormone Receptors: Clinical Implications and Therapeutic Relevance
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- FINASTERIDE INHIBITS 5?-REDUCTASE ACTIVITY IN HUMAN DERMAL FIBROBLASTS: PREDICTION OF ITS THERAPEUTIC APPLICATION IN ANDROGEN-RELATED SKIN DISEASES
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- The Role of Histone Demethylases in Disease
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- A novel hairless highly immunodeficient mice model optimized for in vivo imaging
- Erosive Pustular Dermatosis of the Scalp Due to Afatinib: A Rare Case
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Deletion of adipocyte Sine Oculis Homeobox Homolog 1 prevents lipolysis and attenuates skin fibrosis
- Androgen excess: a hallmark of polycystic ovary syndrome
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- WNT10B (wingless-type MMTV integration site family)
- Lichen Planopilaris
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Modelling androgen synthesis and action during human sexual differentiation
- Insulin Resistance and Polycystic Ovary Syndrome