2023 |
Baer, L., Barthelson, K., Postlethwait, J., Adelson, D., Pederson, S., & Lardelli, M. (2023). Differential allelic representation (DAR) identifies candidate eQTLs and improves transcriptome analysis. bioRxiv. DOI |
2022 |
Barthelson, K., Newman, M., & Lardelli, M. (2022). Brain transcriptomes of zebrafish and mouse Alzheimer's disease knock-in models imply early disrupted energy metabolism. Disease Models and Mechanisms, 15(1), 1-14. DOI Scopus1 WoS1 Europe PMC1 |
2022 |
Allen, A., Barthelson, K., & Lardelli, M. (2022). pHAPE: a plasmid for production of DNA size marker ladders for gel electrophoresis. DOI |
2021 |
Jayne, T., Newman, M., Baer, L., & Lardelli, M. (2021). The evolved divergence of γ-secretase-susceptibility of homologous proteins Ngfrb and Nradd in zebrafish. BMC Research Notes, 14(1), 1-5. DOI |
2021 |
Chin, H. Y., Lardelli, M., Collins-Praino, L., & Barthelson, K. (2021). Differential effects of loss of <i>park7</i> activity on Iron Responsive Element (IRE) gene sets: Implications for the role of iron dyshomeostasis in the pathophysiology of Parkinson’s disease. DOI |
2021 |
Barthelson, K., Pederson, S. M., Newman, M., Jiang, H., & Lardelli, M. (2021). In-Frame and Frameshift Mutations in Zebrafish Presenilin 2 Affect Different Cellular Functions in Young Adult Brains. Journal of Alzheimer's Disease Reports, 5(1), 395-404. DOI Scopus5 Europe PMC3 |
2021 |
Barthelson, K., Dong, Y., Newman, M., & Lardelli, M. (2021). PRESENILIN 1 mutations causing early-onset familial alzheimer's disease or familial acne inversa differ in their effects on genes facilitating energy metabolism and signal transduction. Journal of Alzheimers Disease, 82(1), 327-347. DOI Scopus2 WoS2 Europe PMC3 |
2021 |
Chin, H. Y., Lardelli, M., Collins-Praino, L., & Barthelson, K. (2021). Loss of park7 activity has differential effects on expression of iron responsive element (IRE) gene sets in the brain transcriptome in a zebrafish model of Parkinson's disease.. Mol Brain, 14(1), 83. DOI Scopus6 WoS6 Europe PMC2 |
2021 |
Barthelson, K., Baer, L., Dong, Y., Hand, M., Pujic, Z., Newman, M., . . . Lardelli, M. (2021). Zebrafish Chromosome 14 Gene Differential Expression in the fmr1hu2787 Model of Fragile X Syndrome. Frontiers in Genetics, 12, 1-11. DOI |
2021 |
Hin, N., Newman, M., Pederson, S., & Lardelli, M. (2021). Iron responsive element-mediated responses to iron dyshomeostasis in Alzheimer's disease. Journal of Alzheimers Disease, 84(4), 1-34. DOI Scopus4 WoS5 Europe PMC7 |
2021 |
Hin, N., Newman, M., Pederson, S., & Lardelli, M. (2021). Iron Responsive Element (IRE)-mediated responses to iron dyshomeostasis in Alzheimer's disease. Journal of Alzheimer's Disease, 84(4), 1597-1630. DOI |
2021 |
Barthelson, K., Pederson, S. M., Newman, M., & Lardelli, M. (2021). Brain transcriptome analysis of a protein-truncating mutation in sortilin-related receptor 1 associated with early-onset familial alzheimer's disease indicates early effects on mitochondrial and ribosome function. Journal of Alzheimer's Disease, 79(3), 1105-1119. DOI Scopus4 WoS4 Europe PMC4 |
2021 |
Barthelson, K., Newman, M., Nowell, C. J., & Lardelli, M. (2021). No observed effect on brain vasculature of Alzheimer's disease-related mutations in the zebrafish presenilin 1 gene. Molecular Brain, 14(1), 22-1-22-4. DOI Scopus1 WoS1 Europe PMC1 |
2021 |
Barthelson, K., Dong, Y., Newman, M., & Lardelli, M. (2021). <i>PRESENILIN 1</i>mutations causing early-onset familial Alzheimer’s disease or familial acne inversa differ in their effects on genes facilitating energy metabolism and signal transduction. DOI |
2021 |
Barthelson, K., Newman, M., & Lardelli, M. (2021). Comparative analysis of Alzheimer’s disease knock-in model brain transcriptomes implies changes to energy metabolism as a causative pathogenic stress. DOI |
2021 |
Dong, Y., Newman, M., Pederson, S. M., Barthelson, K., Hin, N., & Lardelli, M. (2021). Transcriptome analyses of 7-day-old zebrafish larvae possessing a familial Alzheimer’s disease-like mutation in psen1 indicate effects on oxidative phosphorylation, ECM and MCM functions, and iron homeostasis. BMC Genomics, 22(1), 211-1-211-16. DOI Scopus6 WoS6 Europe PMC3 |
2021 |
Moussavi Nik, S. H., Porter, T., Newman, M., Bartlett, B., Khan, I., Sabale, M., . . . Verdile, G. (2021). Relevance of a truncated PRESENILIN 2 transcript to Alzheimer's disease and neurodegeneration.. Journal of Alzheimer's Disease, 80(4), 1-11. DOI Scopus1 WoS1 |
2020 |
Barthelson, K., Pederson, S. M., Newman, M., & Lardelli, M. (2020). Brain transcriptome analysis reveals subtle effects on mitochondrial function and iron homeostasis of mutations in the SORL1 gene implicated in early onset familial Alzheimer’s disease. biorxiv. DOI |
2020 |
Jiang, H., Pederson, S. M., Newman, M., Dong, Y., & Lardelli, M. (2020). Transcriptome analysis indicates dominant effects on ribosome and mitochondrial function of a premature termination codon mutation in the zebrafish gene<i>psen2</i>. DOI |
2020 |
Newman, M., Moussavi Nik, S. H., Sutherland, G. T., Hin, N., Kim, W. S., Halliday, G. M., . . . Lardelli, M. (2020). Accelerated loss of hypoxia response in zebrafish with familial Alzheimer's disease-like mutation of Presenilin 1. Human Molecular Genetics, 29(14), 2379-2394. DOI Scopus9 WoS8 Europe PMC6 |
2020 |
Barthelson, K., Newman, M., & Lardelli, M. (2020). Sorting Out the Role of the Sortilin-Related Receptor 1 in Alzheimer's Disease.. J Alzheimers Dis Rep, 4(1), 123-140. DOI Europe PMC10 |
2020 |
Jiang, H., Pederson, S. M., Newman, M., Dong, Y., Barthelson, K., & Lardelli, M. (2020). Transcriptome analysis indicates dominant effects on ribosome and mitochondrial function of a premature termination codon mutation in the zebrafish gene psen2. PLoS One, 15(7), e0232559-1-e0232559-25. DOI Scopus3 WoS3 Europe PMC3 |
2020 |
Barthelson, K., Pederson, S. M., Newman, M., & Lardelli, M. (2020). Brain transcriptome analysis reveals subtle effects on mitochondrial function and iron homeostasis of mutations in the SORL1 gene implicated in early onset familial Alzheimer's disease.. Molecular brain, 13(1), 142. DOI Scopus13 WoS13 Europe PMC8 |
2020 |
Barthelson, K., Pederson, S., Newman, M., & Lardelli, M. (2020). Transcriptome analysis of a protein-truncating mutation in sortilin-related receptor 1 associated with early-onset familial Alzheimer’s disease indicates effects on mitochondrial and ribosome function in young-adult zebrafish brains. biorxiv. DOI |
2020 |
Barthelson, K., Pederson, S. M., Newman, M., Jiang, H., & Lardelli, M. (2020). Frameshift and frame-preserving mutations in zebrafish presenilin 2 affect different cellular functions in young adult brains. DOI |
2020 |
Hin, N., Newman, M., Kaslin, J., Douek, A. M., Lumsden, A., Moussavi Nik, S. H., . . . Lardelli, M. (2020). Accelerated brain aging towards transcriptional inversion in a zebrafish model of the K115fs mutation of human PSEN2. PloS one, 15(1), e0227258. DOI Scopus16 WoS17 Europe PMC14 |
2019 |
Newman, M., Hin, N., Pederson, S., & Lardelli, M. (2019). A familial Alzheimer's disease-like mutation in the zebrafish presenilin 1 gene affects brain energy production. DOI |
2019 |
Newman, M., Nik, H. M., Sutherland, G., Hin, N., Kim, W., Halliday, G., . . . Lardelli, M. (2019). Accelerated loss of hypoxia response in zebrafish with familial Alzheimer’s disease-like mutation of Presenilin 1. DOI |
2019 |
Newman, M., Hin, N., Pederson, S., & Lardelli, M. (2019). Brain transcriptome analysis of a familial Alzheimer's disease-like mutation in the zebrafish presenilin 1 gene implies effects on energy production. Molecular Brain, 12(1), 1-5. DOI Scopus18 WoS18 Europe PMC14 |
2019 |
Braggin, J. E., Bucks, S. A., Course, M. M., Smith, C. L., Sopher, B., Osnis, L., . . . Jayadev, S. (2019). Alternative splicing in a presenilin 2 variant associated with Alzheimer disease. Annals of Clinical and Translational Neurology, 6(4), 762-777. DOI Scopus21 WoS19 Europe PMC14 |
2018 |
Lumsden, A., Rogers, J., Majd, S., Newman, M., Sutherland, G., Verdile, G., & Lardelli, M. (2018). Dysregulation of neuronal iron homeostasis as an alternative unifying effect of mutations causing familial Alzheimer's disease. Frontiers in Neuroscience, 12(AUG), 533-1-533-21. DOI Scopus29 WoS27 Europe PMC18 |
2018 |
Nik, S. H. M., Newman, M., Lumsden, A., Jayne, T., & Lardelli, M. (2018). HMGA1 zebrafish co-orthologue hmga1b can modulate p53-dependent cellular responses but is unable to control the alternative splicing of psen1. DOI |
2018 |
Jiang, H., Newman, M., & Lardelli, M. (2018). The zebrafish orthologue of familial Alzheimer's disease gene PRESENILIN 2 is required for normal adult melanotic skin pigmentation. PLoS ONE, 13(10), e0206155-1-e0206155-20. DOI Scopus15 WoS16 Europe PMC9 |
2018 |
Jiang, H., Jayadev, S., Lardelli, M., & Newman, M. (2018). A Review of the Familial Alzheimer's Disease Locus PRESENILIN 2 and Its Relationship to PRESENILIN 1. Journal of Alzheimer's Disease, 66(4), 1323-1339. DOI Scopus9 WoS9 Europe PMC6 |
2018 |
Ratnayake, D., Newman, M., & Lardelli, M. (2018). Degenerate codon mixing for PCR-based manipulation of highly repetitive sequences. BMC Research Notes, 11(1), 202-1-202-7. DOI Scopus1 Europe PMC1 |
2018 |
Hin, N., Newman, M., Kaslin, J., Douek, A. M., Lumsden, A., Zhou, X., . . . Lardelli, M. (2018). Accelerated brain aging towards transcriptional inversion in a zebrafish model of familial Alzheimer's disease. BioRxiv, OnlinePubl. DOI |
2017 |
Newman, M., Halter, L., Lim, A., & Lardelli, M. (2017). Mitochondrion to endoplasmic reticulum apposition length in zebrafish embryo spinal progenitors is unchanged in response to perturbations associated with Alzheimer’s disease. PLoS ONE, 12(6), e0179859-1-e0179859-17. DOI Scopus2 WoS2 Europe PMC1 |
2016 |
Ebrahimie, E., Moussavi Nik, S., Newman, M., Van Der Hoek, M., & Lardelli, M. (2016). The Zebrafish equivalent of Alzheimer's disease-associated PRESENILIN Isoform PS2V regulates inflammatory and other responses to hypoxic stress. Journal of Alzheimer's Disease, 52(2), 581-608. DOI Scopus14 WoS12 Europe PMC12 |
2016 |
Jayne, T., Newman, M., Verdile, G., Sutherland, G., Münch, G., Musgrave, I., . . . Lardelli, M. (2016). Evidence for and against a pathogenic role of reduced γ-secretase activity in familial Alzheimer's disease. Journal of Alzheimer's Disease, 52(3), 781-799. DOI Scopus27 WoS27 Europe PMC21 |
2016 |
Richards, R., Robertson, S., O'Keefe, L., Fornarino, D., Scott, A., Lardelli, M., & Baune, B. (2016). The enemy within: innate surveillance-mediated cell death, the common mechanism of neurodegenerative disease. Frontiers in Neuroscience, 10(MAY), 193-1-193-20. DOI Scopus27 WoS27 Europe PMC18 |
2015 |
Moussavi Nik, S., Newman, M., Wilson, L., Ebrahimie, E., Wells, S., Musgrave, I., . . . Lardelli, M. (2015). Alzheimer's disease-related peptide PS2V plays ancient, conserved roles in suppression of the unfolded protein response under hypoxia and stimulation of γ-secretase activity. Human Molecular Genetics, 24(13), 3662-3678. DOI Scopus23 WoS21 Europe PMC13 |
2015 |
Lim, A., Moussavi Nik, S., Ebrahimie, E., & Lardelli, M. (2015). Analysis of nicastrin gene phylogeny and expression in zebrafish. Development Genes and Evolution, 225(3), 171-178. DOI Scopus4 WoS4 Europe PMC3 |
2014 |
Newman, M., Ebrahimie, E., & Lardelli, M. (2014). Using the zebrafish model for Alzheimer's disease research. Frontiers in Genetics, 5(JUN), 189-1-189-10. DOI Scopus92 WoS86 Europe PMC45 |
2014 |
Ganesan, S., Moussavi Nik, S., Newman, M., & Lardelli, M. (2014). Identification and expression analysis of the zebrafish orthologues of the mammalian MAP1LC3 gene family. Experimental Cell Research, 328(1), 228-237. DOI Scopus10 WoS11 Europe PMC5 |
2014 |
Nik, S., Croft, K., Mori, T., & Lardelli, M. (2014). The comparison of methods for measuring oxidative stress in zebrafish brains. Zebrafish, 11(3), 248-254. DOI Scopus11 WoS10 Europe PMC7 |
2014 |
Newman, M., Wilson, L., Verdile, G., Lim, A., Khan, I., Nik, S., . . . Lardelli, M. (2014). Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease. Human Molecular Genetics, 23(3), 602-617. DOI Scopus40 WoS38 Europe PMC25 |
2014 |
Moussavi Nik, S. H., Newman, M., Ganesan, S., Chen, M., Martins, R., Verdile, G., & Lardelli, M. (2014). Hypoxia alters expression of Zebrafish Microtubule-associated protein Tau (mapta, maptb) gene transcripts. BMC Research Notes, 7(1), 767-1-767-9. DOI Scopus17 Europe PMC5 |
2014 |
Klarić, T., Lardelli, M., Key, B., Koblar, S., & Lewis, M. (2014). Activity-dependent expression of neuronal PAS domain-containing protein 4 (npas4a) in the developing zebrafish brain. Frontiers in Neuroanatomy, 8(DEC), 148-1-148-13. DOI Scopus15 WoS15 Europe PMC10 |
2013 |
Wilson, L., & Lardelli, M. (2013). The development of an in vivo γ-secretase assay using zebrafish embryos. Journal of Alzheimer's Disease, 36(3), 521-534. DOI Scopus8 WoS8 Europe PMC4 |
2013 |
Sharman, M., Moussavi Nik, S., Chen, M., Ong, D., Wijaya, L., Laws, S., . . . Verdile, G. (2013). The Guinea Pig as a model for sporadic Alzheimer's Disease (AD): the impact of cholesterol intake on expression of AD-related genes. PLoS One, 8(6), 1-12. DOI Scopus30 WoS30 Europe PMC23 |
2012 |
Avdesh, A., Chen, M., Martin-Iverson, M., Mondal, A., Ong, D., Rainey-Smith, S., . . . Martins, R. (2012). Regular care and maintenance of a Zebrafish (Danio rerio) laboratory: an introduction. Journal of Visualized Experiments, (69), 1-8. DOI Scopus234 WoS211 Europe PMC96 |
2012 |
Newman, M., Nornes, S., Martins, R., & Lardelli, M. (2012). Robust homeostasis of Presenilin1 protein levels by transcript regulation. Neuroscience Letters, 519(1), 14-19. DOI Scopus4 WoS5 Europe PMC2 |
2012 |
Moussavi Nik, S., Wilson, L., Newman, M., Croft, K., Mori, T., Musgrave, I., & Lardelli, M. (2012). The BACE1-PSEN-AβPP regulatory axis has an ancient role in response to low oxygen/oxidative stress. Journal of Alzheimer's Disease, 28(3), 515-530. DOI Scopus38 WoS22 Europe PMC24 |
2012 |
Avdesh, A., Martin-Iverson, M., Mondal, A., Chen, M., Askraba, S., Newman, M., . . . Martins, R. (2012). Evaluation of color preference in zebrafish for learning and memory. Journal of Alzheimer's Disease, 28(2), 459-469. DOI Scopus92 WoS86 Europe PMC36 |
2012 |
Chen, M., Tegg, M., Avdesh, A., Mondal, A., Lardelli, M., Verdile, G., & Martins, R. (2012). P4‐121: Analysis of insulin‐degrading enzyme (IDE) expression and function in zebrafish embryos. Alzheimer's & Dementia, 8(4S_Part_18). DOI |
2011 |
Sugano, Y., & Lardelli, M. (2011). Identification and expression analysis of the zebrafish orthologue of Klotho. Development Genes and Evolution, 221(3), 179-186. DOI Scopus11 WoS11 Europe PMC8 |
2011 |
Wells, S., Nornes, S., & Lardelli, M. (2011). Transgenic zebrafish recapitulating tbx16 gene early developmental expression. PLoS One, 6(6), e21559-1-e21559-6. DOI Scopus11 WoS10 Europe PMC8 |
2011 |
Moussavi Nik, S., Newman, M., & Lardelli, M. (2011). The response of HMGA1 to changes in oxygen availability is evolutionarily conserved. Experimental Cell Research, 317(11), 1503-1512. DOI Scopus20 WoS20 Europe PMC16 |
2011 |
Newman, M., Verdile, G., Martins, R., & Lardelli, M. (2011). Zebrafish as a tool in Alzheimer's disease research. Biochimica et Biophysica Acta-Molecular Basis of Disease, 1812(3), 346-352. DOI Scopus52 WoS43 Europe PMC26 |
2010 |
Newman, M., & Lardelli, M. (2010). A hyperactive sleeping beauty transposase enhances transgenesis in zebrafish embryos. BMC Research Notes, 3(1), 282-286. DOI Scopus7 Europe PMC5 |
2010 |
Wells, S., Conran, J., Tamme, R., Gaudin, A., Webb, J., & Lardelli, M. (2010). Cryptic organisation within an apparently irregular rostrocaudal distribution of interneurons in the embryonic zebrafish spinal cord. Experimental Cell Research, 316(19), 3292-3303. DOI Scopus1 WoS1 Europe PMC1 |
2010 |
Newman, M., Wilson, L., Camp-Dotlic, E., Verdile, G., Martins, R., & Lardelli, M. (2010). A zebrafish melanophore model of amyloidβ toxicity. Zebrafish, 7(2), 155-159. DOI Scopus19 WoS19 Europe PMC12 |
2010 |
Aleklett, K., Hook, M., Jakobsson, K., Lardelli, M., Snowden, S., & Soderbergh, B. (2010). The peak of the oil age - Analyzing the world oil production reference scenario in world energy outlook 2008. Energy Policy, 38(3), 1398-1414. DOI Scopus252 WoS199 |
2009 |
Chen, M., Martins, R., & Lardelli, M. (2009). Complex splicing and neural expression of duplicated Tau genes in zebrafish embryos. Journal of Alzheimer's Disease, 18(2), 305-317. DOI Scopus46 WoS41 Europe PMC27 |
2009 |
Henshall, T., Tucker, B., Lumsden, A., Nornes, S., Lardelli, M., & Richards, R. (2009). Selective neuronal requirement for Huntingtin in the developing zebrafish. Human Molecular Genetics, 18(24), 4830-4842. DOI Scopus37 WoS36 Europe PMC30 |
2009 |
Nornes, S., Newman, M., Wells, S., Verdile, G., Martins, R., & Lardelli, M. (2009). Independent and cooperative action of Psen2 with Psen1 in zebrafish embryos. Experimental Cell Research, 316(16), 2791-2801. DOI Scopus39 WoS38 Europe PMC22 |
2009 |
Newman, M., Tucker, B., Nornes, S., Ward, A., & Lardelli, M. (2009). Altering presenilin gene activity in zebrafish embryos causes changes in expression of genes with potential involvement in Alzheimer's Disease pathogenesis. Journal of Alzheimer's Disease, 16(1), 133-147. DOI Scopus25 WoS25 Europe PMC16 |
2009 |
Nornes, S., Tucker, B., & Lardelli, M. (2009). Zebrafish aplnra functions in epiboly. BMC Research Notes, 2(1), 1-6. DOI Scopus7 Europe PMC6 |
2009 |
Lardelli, M. (2009). Mining the data on coal. Science, 324(5929), 880-881. DOI Scopus6 WoS5 |
2009 |
Newman, M., Tucker, B., Nornes, S., Ward, A., & Lardelli, M. (2009). Erratum: Altering presenilin gene activity in zebrafish embryos causes changes in expression of genes with potential involvement in Alzheimer's disease pathogenesis (Journal of Alzheimer's Disease (2009) 16:1 (133-147)). Journal of Alzheimer's Disease, 18(4), 993. DOI |
2008 |
Nornes, S., Newman, M., Verdile, G., Wells, S., Stoick-Cooper, C., Tucker, B., . . . Lardelli, M. (2008). Interference with splicing of Presenilin transcripts has potent dominant negative effects on Presenilin activity. Human Molecular Genetics, 17(3), 402-412. DOI Scopus41 WoS39 Europe PMC24 |
2007 |
Khut, P., Tucker, B., Lardelli, M., & Wood, S. (2007). Evolutionary and expression analysis of the zebrafish deubiquitylating enzyme, Usp9. Zebrafish, 4(2), 95-101. DOI Scopus10 WoS9 Europe PMC7 |
2007 |
Tucker, B., & Lardelli, M. (2007). A rapid apoptosis assay measuring relative acridine orange fluorescence in zebrafish embryos. Zebrafish, 4(2), 113-116. DOI Scopus96 WoS94 Europe PMC54 |
2007 |
Belle, L., Wadham, C., Crocker, L., Lardelli, M., & Khew-Goodall, Y. (2007). The protein tyrosine phosphatase Pez regulates TGFβ, epithelial–mesenchymal transition, and organ development. Journal of Cell Biology, 178(7), 1223-1235. DOI Scopus71 WoS67 Europe PMC50 |
2007 |
Lumsden, A., Henshall, T., Dayan, S., Lardelli, M., & Richards, R. (2007). Huntingtin-deficient zebrafish exhibit defects in iron utilization and development. Human Molecular Genetics, 16(16), 1905-1920. DOI Scopus128 WoS123 Europe PMC90 |
2007 |
Newman, M., Musgrave, I., & Lardelli, M. (2007). Alzheimer disease: amyloidogenesis, the presenilins and animal models. Biochimica et Biophysica Acta-Molecular Basis of Disease, 1772(3), 285-297. DOI Scopus112 WoS101 Europe PMC64 |
2007 |
Lardelli, M. (2007). Scientists need to confront economists about peak oil. Nature, 446(7133), 257. DOI Scopus3 WoS3 Europe PMC1 |
2007 |
Tucker, B., Hepperle, C., Kortschak, R., Rainbird, B., Wells, S., Oates, A., & Lardelli, M. (2007). Zebrafish Angiotensin II receptor-like 1a (agtrl1a) is expressed in migrating hypoblast, vasculature, and in multiple embryonic epithelia. Gene Expression Patterns, 7(3), 258-265. DOI Scopus26 WoS27 Europe PMC23 |
2007 |
Newman, M., Musgrave, I. F., & Lardelli, M. (2007). Corrigendum to "Alzheimer disease: Amyloidogenesis, the presenilins and animal models" [Biochim. Biophys. Acta 1772 (2007) 285-297] (DOI:10.1016/j.bbadis.2006.12.001). Biochimica et Biophysica Acta - Molecular Basis of Disease, 1772(9), 1118. DOI |
2006 |
Tucker, B., Richards, R., & Lardelli, M. (2006). Contribution of mGluR and Fmr1 functional pathways to neurite morphogenesis, craniofacial development and fragile X syndrome. Human Molecular Genetics, 15(23), 3446-3458. DOI Scopus107 WoS103 Europe PMC81 |
2004 |
Tucker, B., Richards, R., & Lardelli, M. (2004). Expression of three zebrafish orthologs of human FMR1-related genes and their phylogenetic relationships. Development Genes and Evolution, 214(11), 567-574. DOI Scopus32 WoS28 Europe PMC20 |
2004 |
Scholpp, S., Groth, C., Lohs, C., Lardelli, M., & Brand, M. (2004). Zebrafish fgfr1 is a member of the fgf8 synexpression group and is required for fgf8 signalling at the midbrain-hindbrain boundary. Development Genes and Evolution, 214(6), 285-295. DOI Scopus61 WoS53 Europe PMC46 |
2003 |
Lardelli, M. (2003). The evolutionary relationships of zebrafish genes tbx6, tbx16/spadetail and mga. Development Genes and Evolution, 213(10), 519-522. DOI Scopus16 WoS17 Europe PMC15 |
2003 |
Camp-Dotlic, E., Badhwar, P., Mann, G., & Lardelli, M. (2003). Expression analysis of a Tyrosinase promoter sequence in zebrafish. Pigment Cell Research, 16(2), 117-126. DOI Scopus14 WoS15 Europe PMC7 |
2003 |
Camp-Dotlic, E., Hope, R., Kortschak, R., Cox, T., & Lardelli, M. (2003). Expression of three spalt (sal) gene homologues in zebrafish embryos. Development Genes and Evolution, 213(1), 35-43. DOI Scopus21 WoS20 Europe PMC18 |
2003 |
Nornes, S., Groth, C., Camp-Dotlic, E., Ey, P., & Lardelli, M. (2003). Developmental control of Presenilin1 expression, endoproteolysis, and interaction in zebrafish embryos. Experimental Cell Research, 289(1), 124-132. DOI Scopus46 WoS42 Europe PMC27 |
2003 |
Lardelli, M. (2003). Something fishy in 21st century genomics. Todays Life Science, 15, 20-23. |
2002 |
Tamme, R., Wells, S., Conran, J., & Lardelli, M. (2002). The identity and distribution of neural cells expressing the mesodermal determinant spadetail. BMC Developmental Biology, 2(9), www 1-www 13. DOI |
2002 |
Groth, C., Nornes, S., Mc Carty, R., Tamme, R., & Lardelli, M. (2002). Identification of a second presenilin gene in zebrafish with similarity to the human Alzheimer's disease gene presenilin2. Development Genes and Evolution, 212(10), 486-490. DOI Scopus55 WoS52 Europe PMC32 |
2002 |
Groth, C., & Lardelli, M. (2002). The structure and function of vertebrate fibroblast growth factor receptor 1. International Journal of Developmental Biology, 46(4 Special Issue SI), 393-400. Scopus72 WoS71 Europe PMC50 |
2002 |
Tamme, R., Wells, S., Conran, J. G., & Lardelli, M. (2002). The identity and distribution of neural cells expressing the mesodermal determinant spadetail.. BMC developmental biology [electronic resource], 2(1), 9. DOI Scopus8 Europe PMC12 |
2002 |
Tamme, R., Wells, S., Conran, J., & Lardelli, M. (2002). The identity and distribution of neural cells expressing the mesodermaldeterminant spadetail. BMC Developmental Biology, 2, 1-13. DOI Scopus14 |
2002 |
Kortschak, R. D., Tamme, R., & Lardelli, M. (2002). Erratum: Evolutionary analysis of vertebrate Notch genes (Development Genes and Evolution (2001) vol. 211 (350-354)). Development Genes and Evolution, 212(3), 158. DOI |
2001 |
Holland, L. Z., Rached, L. A., Tamme, R., Holland, N. D., Kortschak, D., Inoko, H., . . . Lardelli, M. (2001). Erratum: Characterization and developmental expression of the amphioxus homolog of Notch (AmnphiNotch): Evolutionary conservation of multiple expression domains in amphioxus and vertebrates (Developmental Biology (2001) 232:2 (495-507)). Developmental Biology, 233(1), 238. DOI Scopus1 |
2001 |
Jonsson, J., Xiang, Z., Pettersson, M., Lardelli, M., & Nilsson, G. (2001). Distinct and regulated expression of Notch receptors in hematopoietic lineages and during myeloid differentiation. European Journal of Immunology, 31(11), 3240-3247. DOI Scopus44 WoS44 Europe PMC32 |
2001 |
Holland, L., Rached, L., Tamme, R., Holland, N., Inoko, H., Kortschak, R., . . . Lardelli, M. (2001). Characterization and developmental expression of the amphioxus homolog of Notch (AmphiNotch): Evolutionary conservation of multiple expression domains in amphioxus and vertebrates. Developmental Biology, 232(2), 493-507. DOI Scopus50 WoS48 Europe PMC33 |
2001 |
Camp-Dotlic, E., & Lardelli, M. (2001). Tyrosinase gene expression in zebrafish embryos. Development Genes and Evolution, 211(3), 150-153. DOI Scopus64 WoS59 Europe PMC43 |
2001 |
Kortschak, R., Tamme, R., & Lardelli, M. (2001). Evolutionary analysis of vertebrate Notch genes. Development Genes and Evolution, 211(7), 350-354. DOI Scopus28 WoS30 Europe PMC23 |
2001 |
Tamme, R., Mills, K., Rainbird, B., Nornes, S., & Lardelli, M. (2001). Simple, directional cDNA cloning for in situ transcript hybridization screens. Biotechniques, 31(4), 938-946. DOI Scopus6 WoS5 Europe PMC5 |
2000 |
Tamme, R., Camp-Dotlic, E., Kortschak, R., & Lardelli, M. (2000). Non-specific, nested suppression PCR method for isolation of unknown flanking DNA. Biotechniques, 28(5), 895-902. DOI Scopus10 WoS8 Europe PMC6 |
1997 |
Westin, J., & Lardelli, M. (1997). Three novel Notch genes in zebrafish: Implications for vertebrate Notch gene evolution and function. Development Genes and Evolution, 207(1), 51-63. DOI Scopus118 WoS115 Europe PMC65 |
1997 |
Zhang, H. Y., Lardelli, M., & Ekblom, P. (1997). Sequence of zebrafish fibulin-1 and its expression in developing heart and other embryonic organs. Development Genes and Evolution, 207(5), 340-351. DOI Scopus15 WoS14 Europe PMC8 |
1997 |
Lardelli, M. (1997). Generation and PCR screening of bacteriophage gamma sublibraries enriched for rare clones (the "sublibrary method").. Methods in molecular biology (Clifton, N.J.), 67, 345-355. DOI Scopus3 Europe PMC1 |
1996 |
Lardelli, M., Williams, R., Mitsiadis, T., & Lendahl, U. (1996). Expression of the Notch 3 intracellular domain in mouse central nervous system progenitor cells is lethal and leads to disturbed neural tube development. Mechanisms of Development, 59(2), 177-190. DOI Scopus93 WoS91 Europe PMC68 |
1995 |
Dahlstrand, J., Lardelli, M., & Lendahl, U. (1995). Nestin mRNA expression correlates with the central nervous system progenitor cell state in many, but not all, regions of developing central nervous system. Developmental Brain Research, 84(1), 109-129. DOI Scopus446 WoS422 Europe PMC332 |
1995 |
Mitsiadis, T. A., Lardelli, M., Lendahl, U., & Thesleff, I. (1995). Expression of Notch 1, 2, and 3 is regulated by epithelial-mesenchymal interactions and retinoic acid in the developing mouse tooth and associated with determination of ameloblast cell fate. Journal of Cell Biology, 130(2), 407-418. DOI Scopus154 WoS151 Europe PMC113 |
1995 |
Williams, R., Lendahl, U., & Lardelli, M. (1995). Complementary and combinatorial patterns of Notch gene family expression during early mouse development. Mechanisms of Development, 53(3), 357-368. DOI Scopus143 WoS145 Europe PMC98 |
1995 |
Lardelli, M. (1995). Residents’ rights. Nature, 378(6555), 330. DOI |
1995 |
Lardelli, M., Williams, R., & Lendahl, U. (1995). Notch-related genes in animal development. International Journal of Developmental Biology, 39(5), 769-780. Scopus50 WoS50 Europe PMC31 |
1995 |
Lardelli, M. (1995). Discriminatory frontier policy. Nature, 376(6535), 12. DOI |
1994 |
Lardelli, M., Dahlstrand, J., & Lendahl, U. (1994). The novel Notch homologue mouse Notch 3 lacks specific epidermal growth factor-repeats and is expressed in proliferating neuroepithelium. Mechanisms of Development, 46(2), 123-136. DOI Scopus263 WoS275 Europe PMC184 |
1994 |
Larsson, C., Lardelli, M., White, I., & Lendahl, U. (1994). The human NOTCH1, 2, and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated translocation. Genomics, 24(2), 253-258. DOI Scopus84 WoS90 Europe PMC55 |
1994 |
Barlow, C., Meister, B., Lardelli, M., Lendahl, U., & Vennström, B. (1994). Thyroid abnormalities and hepatocellular carcinoma in mice transgenic for v-erbA. EMBO Journal, 13(18), 4241-4250. DOI Scopus74 WoS76 Europe PMC48 |
1994 |
Lardelli, M., & Lendahl, U. (1994). Generating bacteriophage λ sublibraries enriched for rare clones. BioTechniques, 16(3), 420-422. Scopus10 WoS10 Europe PMC7 |
1993 |
Lardelli, M., & Ish-Horowicz, D. (1993). Drosophila hairy pair-rule gene regulates embryonic patterning outside its apparent stripe domains. Development, 118(1), 255-266. DOI Scopus12 WoS12 Europe PMC9 |
1993 |
Lardelli, M., & Lendahl, U. (1993). Motch A and Motch B — Two mouse Notch homologues coexpressed in a wide variety of tissues. Experimental Cell Research, 204(2), 364-372. DOI Scopus121 WoS133 Europe PMC73 |
1989 |
Rushlow, C. A., Hogan, A., Pinchin, S. M., Howe, K. M., Lardelli, M., & Ish-Horowicz, D. (1989). The Drosophila hairy protein acts in both segmentation and bristle patterning and shows homology to N-myc.. The EMBO journal, 8(10), 3095-3103. DOI Scopus164 WoS232 Europe PMC134 |
1989 |
Johnson, M. A., Misra, R. M., Lardelli, M., Messina, M., Ephraums, C., Reeves, P. R., . . . Holmes, I. H. (1989). Synthesis in Escherichia coli of the major glycoprotein of human rotavirus: analysis of the antigenic regions. Gene, 84(1), 73-81. DOI Scopus9 WoS9 Europe PMC9 |
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Lardelli, M. (n.d.). An Alternative View of Familial Alzheimer’s Disease Genetics. DOI |
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Lardelli, M. (n.d.). An Alternative View of Familial Alzheimer’s Disease Genetics. DOI |
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Coulson, M., Searle, I., Richards, R., Tucker, M. R., Bakaj, N., Bertozzi, T., . . . Lardelli, M. (n.d.). Multiple learning and administrative advantages when an advanced course in genetics adopted a “flipped-classroom” format with continuous, online assessment. DOI |