|
| 37988600 | Skeletal Muscle Gene Expression Signatures of Obese High and Low Responders to Endurance Exercise Training. | J Clin Endocrinol Metab | 2024 |
| 37988600 | Skeletal Muscle Gene Expression Signatures of Obese High and Low Responders to Endurance Exercise Training. | J Clin Endocrinol Metab | 2024 |
| 38086776 | Novel markers and networks related to restored skeletal muscle transcriptome after bariatric surgery. | Obesity (Silver Spring) | 2024 |
| 38086776 | Novel markers and networks related to restored skeletal muscle transcriptome after bariatric surgery. | Obesity (Silver Spring) | 2024 |
| 36349687 | Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. | Hum Mol Genet | 2023 |
| 36349687 | Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. | Hum Mol Genet | 2023 |
| 36424672 | Dietary digestible carbohydrates are associated with higher prevalence of asthma in humans and with aggravated lung allergic inflammation in mice. | Allergy | 2023 |
| 36409022 | Aqp5<sup>-/-</sup> mice exhibit reduced maximal body O<sub>2</sub> consumption under cold exposure, normal pulmonary gas exchange, and impaired formation of brown adipose tissue. | Am J Physiol Regul Integr Comp Physiol | 2023 |
| 37608601 | The impact of the cardiovascular component and somatic mutations on ageing. | Aging Cell | 2023 |
| 37603466 | The negative adipogenesis regulator <i>Dlk1</i> is transcriptionally regulated by <i>Ifrd1</i> (TIS7) and translationally by its orthologue <i>Ifrd2</i> (SKMc15). | Elife | 2023 |
| 37968388 | Single-cell, whole-embryo phenotyping of mammalian developmental disorders. | Nature | 2023 |
| 37694284 | Redox state and altered pyruvate metabolism contribute to a dose-dependent metformin-induced lactate production of human myotubes. | Am J Physiol Cell Physiol | 2023 |
| 37769677 | Mechanisms of weight loss-induced remission in people with prediabetes: a post-hoc analysis of the randomised, controlled, multicentre Prediabetes Lifestyle Intervention Study (PLIS). | Lancet Diabetes Endocrinol | 2023 |
| 37414142 | Maternal hyperglycemia induces alterations in hepatic amino acid, glucose and lipid metabolism of neonatal offspring: Multi-omics insights from a diabetic pig model. | Mol Metab | 2023 |
| 37160609 | Knockout mouse models as a resource for the study of rare diseases. | Mamm Genome | 2023 |
| 37468728 | INFRAFRONTIER: mouse model resources for modelling human diseases. | Mamm Genome | 2023 |
| 37467750 | Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease. | Am J Hum Genet | 2023 |
| 36825469 | Knockout mice are an important tool for human monogenic heart disease studies. | Dis Model Mech | 2023 |
| 36774413 | Acute and long-term exercise adaptation of adipose tissue and skeletal muscle in humans: a matched transcriptomics approach after 8-week training-intervention. | Int J Obes (Lond) | 2023 |
| 37326672 | A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in mice. | Mamm Genome | 2023 |
| 37130781 | Deletion of SERF2 in mice delays embryonic development and alters amyloid deposit structure in the brain. | Life Sci Alliance | 2023 |
| 36565314 | Knockout of the Complex III subunit Uqcrh causes bioenergetic impairment and cardiac contractile dysfunction. | Mamm Genome | 2023 |
| 36993625 | Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT). | medRxiv | 2023 |
| 36538124 | A rationale for considering heart/brain axis control in neuropsychiatric disease. | Mamm Genome | 2023 |
| 37429525 | Differences in DNA methylation of HAMP in blood cells predicts the development of type 2 diabetes. | Mol Metab | 2023 |
| 37294348 | Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice. | Mamm Genome | 2023 |
| 37230398 | AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease. | Biochim Biophys Acta Mol Basis Dis | 2023 |
| 37352860 | Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans. | Am J Hum Genet | 2023 |
| 37221250 | Echo2Pheno: a deep-learning application to uncover echocardiographic phenotypes in conscious mice. | Mamm Genome | 2023 |
| 37694284 | Redox state and altered pyruvate metabolism contribute to a dose-dependent metformin-induced lactate production of human myotubes. | Am J Physiol Cell Physiol | 2023 |
| 37608601 | The impact of the cardiovascular component and somatic mutations on ageing. | Aging Cell | 2023 |
| 37769677 | Mechanisms of weight loss-induced remission in people with prediabetes: a post-hoc analysis of the randomised, controlled, multicentre Prediabetes Lifestyle Intervention Study (PLIS). | Lancet Diabetes Endocrinol | 2023 |
| 37603466 | The negative adipogenesis regulator <i>Dlk1</i> is transcriptionally regulated by <i>Ifrd1</i> (TIS7) and translationally by its orthologue <i>Ifrd2</i> (SKMc15). | Elife | 2023 |
| 37968388 | Single-cell, whole-embryo phenotyping of mammalian developmental disorders. | Nature | 2023 |
| 37326672 | A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in mice. | Mamm Genome | 2023 |
| 37221250 | Echo2Pheno: a deep-learning application to uncover echocardiographic phenotypes in conscious mice. | Mamm Genome | 2023 |
| 37160609 | Knockout mouse models as a resource for the study of rare diseases. | Mamm Genome | 2023 |
| 36993625 | Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT). | medRxiv | 2023 |
| 37352860 | Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans. | Am J Hum Genet | 2023 |
| 37414142 | Maternal hyperglycemia induces alterations in hepatic amino acid, glucose and lipid metabolism of neonatal offspring: Multi-omics insights from a diabetic pig model. | Mol Metab | 2023 |
| 37468728 | INFRAFRONTIER: mouse model resources for modelling human diseases. | Mamm Genome | 2023 |
| 37467750 | Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease. | Am J Hum Genet | 2023 |
| 37230398 | AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease. | Biochim Biophys Acta Mol Basis Dis | 2023 |
| 37130781 | Deletion of SERF2 in mice delays embryonic development and alters amyloid deposit structure in the brain. | Life Sci Alliance | 2023 |
| 37429525 | Differences in DNA methylation of HAMP in blood cells predicts the development of type 2 diabetes. | Mol Metab | 2023 |
| 37294348 | Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice. | Mamm Genome | 2023 |
| 36409022 | Aqp5<sup>-/-</sup> mice exhibit reduced maximal body O<sub>2</sub> consumption under cold exposure, normal pulmonary gas exchange, and impaired formation of brown adipose tissue. | Am J Physiol Regul Integr Comp Physiol | 2023 |
| 36774413 | Acute and long-term exercise adaptation of adipose tissue and skeletal muscle in humans: a matched transcriptomics approach after 8-week training-intervention. | Int J Obes (Lond) | 2023 |
| 36538124 | A rationale for considering heart/brain axis control in neuropsychiatric disease. | Mamm Genome | 2023 |
| 36424672 | Dietary digestible carbohydrates are associated with higher prevalence of asthma in humans and with aggravated lung allergic inflammation in mice. | Allergy | 2023 |