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Research 541–570 of 1000+
- Structures of Get3d reveal a distinct architecture associated with the emergence of photosynthesis
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Developmental genetics of color pattern establishment in cats
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Association of atopic dermatitis with autoimmune diseases: A bidirectional and multivariable two-sample mendelian randomization study
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- RETRACTED: Interleukin‐33 links asthma to alopecia areata: Mendelian randomization and mediation analysis
- RETRACTED: Genetic association between asthma and alopecia areata: A two‐sample Mendelian randomization study
- RETRACTED: Explore the genetic exposure to alopecia areata
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Exploring the Impact of Systemic Inflammatory Regulators on Rosacea Risk: A Bidirectional Mendelian Randomization Analysis
- The causal relationship between androgenetic alopecia and serum uric acid: A bidirectional Mendelian randomization analysis
- Influência da atividade física regular no controle da progresão da alopecia androgenética masculina: uma revisão de literatura
- Causal effects of glutamine and lipid-related metabolites on alopecia areata: A 2-sample Mendelian randomization study
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Causal effects of genetically determined metabolites on androgenetic alopecia: A two‐sample Mendelian randomization analysis
- Identification of VLDL as a biomarker for prewarning of androgenic alopecia
- Association between non-scarring alopecia and hypothyroidism: a bidirectional two-sample Mendelian randomization study
- Epidemiologic Study of Gene Distribution in Romanian and Brazilian Patients with Non-Cicatricial Alopecia
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Keratin intermediate filaments in the colon: guardians of epithelial homeostasis
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Machine learning driven multi-omics analysis of the genetic mechanisms behind the double-coat fleece formation in Hetian sheep
- Differential expression of steroid 5α-reductase isozymes and association with disease severity and angiogenic genes predict their biological role in prostate cancer