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Research 481–510 of 1000+
- MICRONEEDLING WITH PLATELET-RICH PLASMA VERSUS MICRONEEDLING WITH TOPICAL 5% MINOXIDIL IN PATIENTS WITH ANDROGENETIC ALOPECIA- A COMPARATIVE STUDY
- Can plant‐derived phytochemicals provide symptom relief for hair loss? A critical review
- Phytoconstituents and Antioxidant Profiling of Avicennia marina (Forsk.) Vierh. Heartwood Extract Sourced from Bagan Kuala: A Novel Natural Source for Radical Scavenging Applications
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- Hardwiring Stem Cell Communication through Tissue Structure
- An overview of the genetic aspects of hair loss and its connection with nutrition
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Art’s Work in the Age of Biotechnology: Shaping Our Genetic Futures
- Molecular Genetics of Human Hair Diseases
- Low Heterozygosity and Historical Bottleneck Effect Depicted From the Genome Assembly of the Indus River Dolphin (<i>Platanista minor</i>)
- Genomic Characterization of Quality Wool Traits in Spanish Merino Sheep
- 0040 Machine learning algorithms as tools for identifying predictive autoantibody biomarkers in pemphigus vulgaris
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- The Rotterdam Study: 2016 objectives and design update
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility