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Research 631–660 of 1000+
- Causal relationship between gut microbiota and androgenetic alopecia: A Mendelian randomization study
- Genome-Wide Association Studies of Hair Whorl in Pigs
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Association between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Keratin disorders: from gene to therapy
- Fabrication of Bilayer Nanofibrous-Hydrogel Scaffold from <i>Bacterial Cellulose</i>, <i>PVA</i>, and <i>Gelatin</i> as Advanced Dressing for Wound Healing and Soft Tissue Engineering
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- 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)
- Nrf2-Mediated Expansion of Pilosebaceous Cells Accelerates Cutaneous Wound Healing
- 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
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Regulation of masculinization: androgen signalling for external genitalia development
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Silk Fibroin and Its Nanocomposites for Wound Care: A Comprehensive Review
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles