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Research 721–750 of 1000+
- 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
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Restoration of Spermatogenesis and Male Fertility Using an Androgen Receptor Transgene
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms
- Progress and prospects: gene therapy for performance and appearance enhancement
- Genome-wide detection and sequence conservation analysis of long non-coding RNA during hair follicle cycle of yak
- An important role of podoplanin in hair follicle growth
- Developing Patient-Derived 3D-Bioprinting models of pancreatic cancer
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Evaluation of noninvasive biospecimens for transcriptome studies
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
- Time-course RNA-seq analysis reveals stage-specific and melatonin-triggered gene expression patterns during the hair follicle growth cycle in Capra hircus
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- Identification of functional circRNAs regulating ovarian follicle development in goats
- LGR5 is a conserved marker of hair follicle stem cells in multiple species and is present early and throughout follicle morphogenesis
- Homozygous whole body <i>Cbs</i> knockout in adult mice features minimal pathology during ageing despite severe homocysteinemia
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- Effect of CUX1 on the Proliferation of Hu Sheep Dermal Papilla Cells and on the Wnt/β-Catenin Signaling Pathway
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Pitfalls of PCR-Based Strategy for Genotyping <i>Cre-Loxp</i> Mice
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis
- The role of <i>Atg5</i> gene in tumorigenesis under autophagy deficiency conditions
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies