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Research 631–660 of 1000+
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Chronic overlapping pain conditions and nociplastic pain
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Gut instinct: Using tofacitinib to treat alopecia areata in the context of comorbid inflammatory bowel disease
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Copper Deficiency a New Reason of Androgenetic Alopecia?
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Unraveling Translational Insights into Systemic Multi-Organ Toxicity of Cytosine Arabinoside (Ara-C): A Systematic Review of Preclinical Animal Evidence
- 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
- <i>Alpinia zerumbet</i>: A Review of the Chemistry, Quantity, and Pharmacological Properties of Selected Kavalactones
- Regulatory pathways implicated in male androgenetic alopecia pathogenesis
- Counting Hairs: Is It Androgenetic Alopecia or Chronic Telogen Effluvium?
- Drug Discovery Today: Therapeutic Strategies - 2006 Editorial
- Healthy Hair: Form and Function
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Molecular basis of congenital atrichia in humans and mice.
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Tracing the cellular origin of cancer
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Building a hair: tip growth in<i>Arabidopsis thaliana</i>root hairs
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Keratin disorders: from gene to therapy
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Regulation of masculinization: androgen signalling for external genitalia development
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- The molecular pathogenesis of Trichilemmal carcinoma
- Skin precancer.