Genetics & genomics
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3,213 studies
- Targeting JAK/STAT Signaling Attenuates Postoperative Recurrence in an HLA-B27 Transgenic Rat Model of Crohn’s Disease
- Genetic and multi-omic insights into inflammation and metabolism in a French Polynesian cohort
- Education-related polygenic scores show different associations with youth mental health in parent-offspring trios
- Mutualistic microbes linked to broader niches but reduced diversification
- Evaluation of γδ T cells in autosomal dominant polycystic kidney disease
- Sequence-aware genotyping improves the accuracy of molecular markers associated with cassava mosaic disease resistance loci
- Genomic characterization and selection signals in Italian black Atriana chickens using high-density SNP array
- Refining the genetic architecture of myocardial infarction through integrative post-genome-wide association study functional genomics analysis
- Molecular and morphological characterization of nine new Gnomoniopsis species (Diaporthales, Gnomoniaceae): Genomic insights into evolution and phylogeny
- Integrative Genomic Analyses Prioritize CETP-Related Lipid Traits in Age-Related Macular Degeneration
- Genetic and Clinical Characterization of Early-Onset High Myopia With or Without Cataract Due to Biallelic P3H2 Variants
- The revised diploid genome sequence of an individual human: A workflow for near telomere-to-telomere assemblies using only Oxford Nanopore Technologies Simplex-reads
- A multi-year (2007-2025) moth community dataset across the islands of southern South Korea
- Predictors, risk factors and management of intestinal failure in crohn’s disease: A narrative review
- Chiari I malformation risk across anatomical subtypes of sagittal synostosis
- DECIPHERING DIAMOND-BLACKFAN ANEMIA GERMLINE VARIANTS: CHARACTERIZING A BRAZILIAN COHORT AGAINST INTERNATIONAL COHORTS
- RESPOSTA À TERAPIA IMUNOSSUPRESSORA EM PACIENTE COM HIPOPLASIA MEDULAR AUTOIMUNE: RELATO DE CASO
- EPIDEMIOLOGIA DAS ALTERAÇÕES CROMOSSÔMICAS RECORRENTES EM NEOPLASIAS HEMATOLÓGICAS: ANÁLISE DE 804 CARIÓTIPOS E RELEVÂNCIA DA CITOGENÉTICA CONVENCIONAL
- COMPONENTES BIOATIVOS DA PEÇONHA DE
- MOLECULAR INVESTIGATION OF CHILDREN WITH SUSPECTED BONE MARROW FAILURE SYNDROMES AT A PEDIATRIC REFERRAL CENTER WITHIN THE BRAZILIAN UNIFIED HEALTH SYSTEM: RESULTS OF AN INTERDISCIPLINARY APPROACH
- GENOME-WIDE COPY NUMBER VARIATIONS REVEAL DISTINCT GENOMIC SIGNATURES IN AN ADMIXED BRAZILIAN COHORT WITH MYELODYSPLASTIC NEOPLASMS
- ASSOCIAÇÃO ENTRE ANEMIA DE FANCONI E SÍNDROME VACTERL: RELATO DE DOIS CASOS
- AVALIAÇÃO DE RESPOSTA NO ACRÉSCIMO DO ELTROMBOPAG PARA TRATAMENTO IMUNOSSUPRESSOR DA APLASIA DE MEDULA
- PERFIL HEMATOLÓGICO E VARIABILIDADE INTRAINDIVIDUAL DA CONTAGEM DE NEUTRÓFILOS EM PACIENTES COM NEUTROPENIA CRÔNICA DE ETIOLOGIA INDEFINIDA: RESULTADOS PRELIMINARES DE UM ESTUDO RETROSPECTIVO
- CARACTERIZAÇÃO FUNCIONAL DE VARIANTES PATOGÊNICAS E PROVAVELMENTE PATOGÊNICAS EM UMA COORTE DE PACIENTES COM DOENÇAS RARAS DE MANIFESTAÇÕES HEMATOLÓGICAS