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Research 631–660 of 1000+
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- FGF5 is a crucial regulator of hair length in humans
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Variables affecting the potential efficacy of PRP in providing chronic pain relief
- Drug repurposing: A novel strategy to target cancer stem cells and therapeutic resistance
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Unravelling the molecular basis for symbiotic signal transduction in legumes
- Bioavailability Enhancement of Cepharanthine via Pulmonary Administration in Rats and Its Therapeutic Potential for Pulmonary Fibrosis Associated with COVID-19 Infection
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Biomimetic Cell Membrane‐Coated Scaffolds for Enhanced Tissue Regeneration
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Glucoraphanin and sulforaphane biosynthesis by melatonin mediating nitric oxide in hairy roots of broccoli (Brassica oleracea L. var. italica Planch): insights from transcriptome data
- Stem Cell Secretome for Skincare: Of Cell Types, Exosomes, Extracellular Vesicles, and Soluble Fractions
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Safety First: A Comprehensive Review of Nutritional Supplements for Hair Loss in Breast Cancer Patients
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome