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Research 571–600 of 1000+
- The Dark Side of Gefitinib: Reflectance Confocal Microscopy Applied to Hair Hyperpigmentation
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Cell Surface B2m-Free Human Leukocyte Antigen (HLA) Monomers and Dimers: Are They Neo-HLA Class and Proto-HLA?
- Azathioprine‐induced severe myelosuppression accompanied by massive hair loss and painful oral ulcer in an autoimmune hepatitis patient with <i>NUDT15</i> minor variant: A case report
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Exploiting the origins of Ras mediated squamous cell carcinoma to develop novel therapeutic interventions
- Ear pinna growth and differentiation is conserved in murids and requires BMP signaling for chondrocyte proliferation
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- TRPV3 Ion Channel: From Gene to Pharmacology
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- Loss of Dicer in Newborn Melanocytes Leads to Premature Hair Graying and Changes in Integrin Expression
- The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal
- Role of Sulfur Metabolism Gene and High-Sulfur Gene Expression in Wool Growth Regulation in the Cashmere Goat
- Skin Stearoyl-CoA Desaturase Genes
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- Sdr16c5 and Sdr16c6 control a dormant pathway at a bifurcation point between meibogenesis and sebogenesis
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- New frontiers in CRISPR/Cas9 delivery systems delivery for gene editing
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Author response: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Improving human forensics through advances in genetics, genomics and molecular biology