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John M. Joslin, Ph.D. - Publications

Affiliations: 
2006 University of Chicago, Chicago, IL 
Area:
Genetics, Medical Biophysics, Oncology
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7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2010 Qian Z, Joslin JM, Tennant TR, Reshmi SC, Young DJ, Stoddart A, Larson RA, Le Beau MM. Cytogenetic and genetic pathways in therapy-related acute myeloid leukemia. Chemico-Biological Interactions. 184: 50-7. PMID 19958752 DOI: 10.1016/J.Cbi.2009.11.025  0.556
2007 Joslin JM, Fernald AA, Tennant TR, Davis EM, Kogan SC, Anastasi J, Crispino JD, Le Beau MM. Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disorders. Blood. 110: 719-26. PMID 17420284 DOI: 10.1182/Blood-2007-01-068809  0.587
2005 Joslin JM, Fernald AA, Qian Z, Crispino JD, Le Beau MM. Egr1, a Candidate Gene within the Commonly Deleted Segment of Chromosome 5, Plays a Role in Murine Erythropoiesis and Leukemogenesis. Blood. 106: 663-663. DOI: 10.1182/Blood.V106.11.663.663  0.605
2002 Wheeler RB, Sharp JD, Schultz RA, Joslin JM, Williams RE, Mole SE. The gene mutated in variant late-infantile neuronal ceroid lipofuscinosis (CLN6) and in nclf mutant mice encodes a novel predicted transmembrane protein. American Journal of Human Genetics. 70: 537-42. PMID 11727201 DOI: 10.1086/338708  0.436
2001 Sharp JD, Wheeler RB, Schultz RA, Joslin JM, Mole SE, Williams RE, Gardiner RM. Analysis of candidate genes in the CLN6 critical region using in silico cloning. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 5: 29-31. PMID 11589002 DOI: 10.1053/Ejpn.2000.0430  0.447
2001 Lai F, Godley LA, Joslin J, Fernald AA, Liu J, Espinosa R, Zhao N, Pamintuan L, Till BG, Larson RA, Qian Z, Le Beau MM. Transcript map and comparative analysis of the 1.5-Mb commonly deleted segment of human 5q31 in malignant myeloid diseases with a del(5q). Genomics. 71: 235-45. PMID 11161817 DOI: 10.1006/Geno.2000.6414  0.552
2000 Ji Y, Rebert NA, Joslin JM, Higgins MJ, Schultz RA, Nicholls RD. Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human. Genome Research. 10: 319-29. PMID 10720573 DOI: 10.1101/gr.10.3.319  0.529
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