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Research 931–960 of 1000+
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Regulation of masculinization: androgen signalling for external genitalia development
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Keratins: the hair shaft's backbone revealed
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Predicting Human Appearance from DNA for Forensic Investigations
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- 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
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Interleukin 15 Gene Polymorphism in patients with Alopecia Areata
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- 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
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Gut instinct: Using tofacitinib to treat alopecia areata in the context of comorbid inflammatory bowel disease