Search
for
Sort by
Research 571–600 of 1000+
- Hair Depigmentation Is a Biological Readout for Pharmacological Inhibition of KIT in Mice and Humans
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Hair loss in children.
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Chronic overlapping pain conditions and nociplastic pain
- Transcriptional Characteristics Showed That miR-144-y/FOXO3 Participates in Embryonic Skin and Feather Follicle Development in Zhedong White Goose
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- Admixture in Latin America: Geographic Structure, Phenotypic Diversity and Self-Perception of Ancestry Based on 7,342 Individuals
- An observational study of the association between androgenetic alopecia and size of the prostate
- Can we predict prostate size by scoring baldness? The relationship of androgenic alopecia and lower urinary tract symptoms.
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Association Between Trichoscopic Features and Serum Hormone Levels and Vitamin D Concentration in Patients with Androgenetic Alopecia in Eastern China: A Cross-Sectional Study
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Anti-Müllerian hormone gene polymorphism is associated with androgen levels in Chinese polycystic ovary syndrome patients with insulin resistance
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Author response: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Red Blood Cells Folate Level in Patients with Alopecia Areata
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- FOXN1 deficient nude severe combined immunodeficiency
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Regulatory pathway analysis of coat color genes in Mongolian horses
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Genome-Wide Association Study for Body Conformation Traits in Kazakh Fat-Tailed Coarse-Wool Sheep
- Depressive Disorder and Dermatological Autoimmune Diseases
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep