Neuraminidase-1 variation among mice carrying t chromosomes

Analysis of Campylobacter jejuni isolates of various sources for loci associated with Guillain-Barré Syndrome.

European journal of microbiology & immunology·2014

[Proximal femoral fractures in the German external quality assurance module 17/1: reasons for delay in surgery].

Der Unfallchirurg·2013

Urogenital chlamydiosis among Slovak women.

Bratislavske lekarske listy·2013

Epithelial response to high-grain diets involves alteration in nutrient transporters and Na+/K+-ATPase mRNA expression in rumen and colon of goats.

Journal of animal science·2013

Is apoptosis a regulatory mechanism during early canine pregnancy?

Reproduction in domestic animals = Zuchthygiene·2013

Prevalence and risk factors for shedding of thermophilic Campylobacter in calves with and without diarrhea in Austrian dairy herds.

Journal of dairy science·2012

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Immunogenetics·2026

Genetic association of immunosenescence to immune decline.

Immunogenetics·2026

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Immunogenetics·2026

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Immunogenetics·2026

Elevated interleukin-36γ and gene polymorphisms implicate novel risk in essential hypertension.

Immunogenetics·2026

Unraveling the genomic structures, conserved functional domains and evolutionary dynamics of beta-defensins in Bubalus bubalis and Ovis aries.

Immunogenetics·2026

Phenotypes of Hereditary Diseases Associated With Rauch-Steindl Syndrome.

Human mutation·2026

Multi-omics Mendelian Randomization Prioritizes Neutrophil Extracellular Trap-related Genes Associated with Atrial Fibrillation Risk.

Endocrine, metabolic & immune disorders drug targets·2026

Developmental and cellular vulnerabilities underlie genetic architecture of schizophrenia.

Molecular psychiatry·2026

Methodological frameworks to probe histone acetylation-driven circuit plasticity in SYNGAP1-associated neurodevelopmental disorders.

Methods in enzymology·2026

Exploring the genetic spectrum of parkinsonism in Brazil.

Parkinsonism & related disorders·2026

Genetic Testing for Neuromuscular Diseases.

Practical neurology (Fort Washington, Pa.)·2026

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Neuraminidase-1 variation among mice carrying t chromosomes

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Analysis of Campylobacter jejuni isolates of various sources for loci associated with Guillain-Barré Syndrome.

[Proximal femoral fractures in the German external quality assurance module 17/1: reasons for delay in surgery].

Urogenital chlamydiosis among Slovak women.

Epithelial response to high-grain diets involves alteration in nutrient transporters and Na+/K+-ATPase mRNA expression in rumen and colon of goats.

Is apoptosis a regulatory mechanism during early canine pregnancy?

Prevalence and risk factors for shedding of thermophilic Campylobacter in calves with and without diarrhea in Austrian dairy herds.

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Genetic association of immunosenescence to immune decline.

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Elevated interleukin-36γ and gene polymorphisms implicate novel risk in essential hypertension.

Unraveling the genomic structures, conserved functional domains and evolutionary dynamics of beta-defensins in Bubalus bubalis and Ovis aries.

Phenotypes of Hereditary Diseases Associated With Rauch-Steindl Syndrome.

Multi-omics Mendelian Randomization Prioritizes Neutrophil Extracellular Trap-related Genes Associated with Atrial Fibrillation Risk.

Developmental and cellular vulnerabilities underlie genetic architecture of schizophrenia.

Methodological frameworks to probe histone acetylation-driven circuit plasticity in SYNGAP1-associated neurodevelopmental disorders.

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Neuraminidase-1 variation among mice carrying t chromosomes

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