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Research 421–450 of 1000+
- 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
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- Molecular and Pathological Studies on Sarcoptes scabiei in Sheep in Ismailia Province, Egypt.
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Chronic overlapping pain conditions and nociplastic pain
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Generalized atrophic benign epidermolysis bullosa.
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Regulation of masculinization: androgen signalling for external genitalia development
- 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)
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Skin precancer.
- Regulatory pathway analysis of coat color genes in Mongolian horses
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Childhood Alopecia Areata: An Overview of Treatment and Recent Patents
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Genome-Wide Association Study for Body Conformation Traits in Kazakh Fat-Tailed Coarse-Wool Sheep