| Year |
Citation |
Score |
| 2007 |
Peery EG, Elmore MD, Resnick JL, Brannan CI, Johnstone KA. A targeted deletion upstream of Snrpn does not result in an imprinting defect. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 255-62. PMID 17514346 DOI: 10.1007/S00335-007-9019-3 |
0.478 |
|
| 2006 |
Johnstone KA, DuBose AJ, Futtner CR, Elmore MD, Brannan CI, Resnick JL. A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects. Human Molecular Genetics. 15: 393-404. PMID 16368707 DOI: 10.1093/Hmg/Ddi456 |
0.519 |
|
| 2004 |
Chamberlain SJ, Johnstone KA, DuBose AJ, Simon TA, Bartolomei MS, Resnick JL, Brannan CI. Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice. Human Molecular Genetics. 13: 2971-7. PMID 15459179 DOI: 10.1093/Hmg/Ddh314 |
0.5 |
|
| 2004 |
Landers M, Bancescu DL, Le Meur E, Rougeulle C, Glatt-Deeley H, Brannan C, Muscatelli F, Lalande M. Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn. Nucleic Acids Research. 32: 3480-92. PMID 15226413 DOI: 10.1093/Nar/Gkh670 |
0.427 |
|
| 2002 |
Barbour KW, Wei F, Brannan C, Flotte TR, Baumann H, Berger FG. The Murine α1-Proteinase Inhibitor Gene Family: Polymorphism, Chromosomal Location, and Structure Genomics. 80: 515-522. DOI: 10.1006/Geno.2002.6864 |
0.436 |
|
| 2001 |
Brannan CI, Disteche CM, Park LS, Copeland NG, Jenkins NA. Autosomal telomere exchange results in the rapid amplification and dispersion of Csf2ra genes in wild-derived mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 882-6. PMID 11707773 DOI: 10.1007/S00335-001-2084-0 |
0.498 |
|
| 2001 |
Blaydes SM, Kogan SC, Truong BT, Gilbert DJ, Jenkins NA, Copeland NG, Largaespada DA, Brannan CI. Retroviral integration at the Epi1 locus cooperates with Nf1 gene loss in the progression to acute myeloid leukemia. Journal of Virology. 75: 9427-34. PMID 11533205 DOI: 10.1128/Jvi.75.19.9427-9434.2001 |
0.645 |
|
| 2001 |
Chamberlain SJ, Brannan CI. The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a. Genomics. 73: 316-22. PMID 11350123 DOI: 10.1006/Geno.2001.6543 |
0.501 |
|
| 2001 |
Costa RM, Yang T, Huynh DP, Pulst SM, Viskochil DH, Silva AJ, Brannan CI. Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1. Nature Genetics. 27: 399-405. PMID 11279521 DOI: 10.1038/86898 |
0.329 |
|
| 2001 |
El-Maarri O, Buiting K, Peery EG, Kroisel PM, Balaban B, Wagner K, Urman B, Heyd J, Lich C, Brannan CI, Walter J, Horsthemke B. Maternal methylation imprints on human chromosome 15 are established during or after fertilization. Nature Genetics. 27: 341-4. PMID 11242121 DOI: 10.1038/85927 |
0.484 |
|
| 2000 |
Cavaillé J, Buiting K, Kiefmann M, Lalande M, Brannan CI, Horsthemke B, Bachellerie JP, Brosius J, Hüttenhofer A. Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization. Proceedings of the National Academy of Sciences of the United States of America. 97: 14311-6. PMID 11106375 DOI: 10.1073/Pnas.250426397 |
0.452 |
|
| 2000 |
Lee S, Kozlov S, Hernandez L, Chamberlain SJ, Brannan CI, Stewart CL, Wevrick R. Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype. Human Molecular Genetics. 9: 1813-9. PMID 10915770 DOI: 10.1093/Hmg/9.12.1813 |
0.491 |
|
| 2000 |
Bielinska B, Blaydes SM, Buiting K, Yang T, Krajewska-Walasek M, Horsthemke B, Brannan CI. De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch. Nature Genetics. 25: 74-8. PMID 10802660 DOI: 10.1038/75629 |
0.666 |
|
| 1999 |
Blaydes SM, Elmore M, Yang T, Brannan CI. Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 549-55. PMID 10341083 DOI: 10.1007/S003359901042 |
0.665 |
|
| 1998 |
Yang T, Adamson TE, Resnick JL, Leff S, Wevrick R, Francke U, Jenkins NA, Copeland NG, Brannan CI. A mouse model for Prader-Willi syndrome imprinting-centre mutations. Nature Genetics. 19: 25-31. PMID 9590284 DOI: 10.1038/Ng0598-25 |
0.56 |
|
| 1996 |
Largaespada DA, Brannan CI, Shaughnessy JD, Jenkins NA, Copeland NG. The neurofibromatosis type 1 (NF1) tumor suppressor gene and myeloid leukemia. Current Topics in Microbiology and Immunology. 211: 233-9. PMID 8585954 DOI: 10.1007/978-3-642-85232-9_23 |
0.362 |
|
| 1996 |
Largaespada DA, Brannan CI, Jenkins NA, Copeland NG. Nf1 deficiency causes Ras-mediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia. Nature Genetics. 12: 137-43. PMID 8563750 DOI: 10.1038/Ng0296-137 |
0.387 |
|
| 1995 |
Valenzuela DM, Rojas E, Le Beau MM, Espinosa R, Brannan CI, McClain J, Masiakowski P, Ip NY, Copeland NG, Jenkins NA. Genomic organization and chromosomal localization of the human and mouse genes encoding the alpha receptor component for ciliary neurotrophic factor. Genomics. 25: 157-63. PMID 7774913 DOI: 10.1016/0888-7543(95)80121-2 |
0.399 |
|
| 1995 |
Vogel KS, Brannan CI, Jenkins NA, Copeland NG, Parada LF. Loss of neurofibromin results in neurotrophin-independent survival of embryonic sensory and sympathetic neurons. Cell. 82: 733-42. PMID 7671302 DOI: 10.1016/0092-8674(95)90470-0 |
0.32 |
|
| 1995 |
Nordlund ML, Rizvi TA, Brannan CI, Ratner N. Neurofibromin expression and astrogliosis in neurofibromatosis (type 1) brains. Journal of Neuropathology and Experimental Neurology. 54: 588-600. PMID 7602332 DOI: 10.1097/00005072-199507000-00013 |
0.336 |
|
| 1995 |
Bedell MA, Brannan CI, Evans EP, Copeland NG, Jenkins NA, Donovan PJ. DNA rearrangements located over 100 kb 5' of the Steel (Sl)-coding region in Steel-panda and Steel-contrasted mice deregulate Sl expression and cause female sterility by disrupting ovarian follicle development. Genes & Development. 9: 455-70. PMID 7533739 DOI: 10.1101/Gad.9.4.455 |
0.423 |
|
| 1994 |
Ito Y, Seto Y, Brannan CI, Copeland NG, Jenkins NA, Fukunaga R, Nagata S. Structural analysis of the functional gene and pseudogene encoding the murine granulocyte colony-stimulating-factor receptor. European Journal of Biochemistry / Febs. 220: 881-91. PMID 8143742 DOI: 10.1111/J.1432-1033.1994.Tb18691.X |
0.464 |
|
| 1994 |
Brannan CI, Perkins AS, Vogel KS, Ratner N, Nordlund ML, Reid SW, Buchberg AM, Jenkins NA, Parada LF, Copeland NG. Targeted disruption of the neurofibromatosis type-1 gene leads to developmental abnormalities in heart and various neural crest-derived tissues. Genes & Development. 8: 1019-29. PMID 7926784 DOI: 10.1101/Gad.8.9.1019 |
0.436 |
|
| 1993 |
Goodwin RG, Din WS, Davis-Smith T, Anderson DM, Gimpel SD, Sato TA, Maliszewski CR, Brannan CI, Copeland NG, Jenkins NA. Molecular cloning of a ligand for the inducible T cell gene 4-1BB: a member of an emerging family of cytokines with homology to tumor necrosis factor. European Journal of Immunology. 23: 2631-41. PMID 8405064 DOI: 10.1002/Eji.1830231037 |
0.369 |
|
| 1993 |
Smith CA, Gruss HJ, Davis T, Anderson D, Farrah T, Baker E, Sutherland GR, Brannan CI, Copeland NG, Jenkins NA, Grabstein KH, Gliniak B, McAlister IB, Fanslow W, Alderson M, et al. CD30 antigen, a marker for Hodgkin's lymphoma, is a receptor whose ligand defines an emerging family of cytokines with homology to TNF Cell. 73: 1349-1360. PMID 8391931 DOI: 10.1016/0092-8674(93)90361-S |
0.356 |
|
| 1993 |
Disteche CM, Brannan CI, Larsen A, Adler DA, Schorderet DF, Gearing D, Copeland NG, Jenkins NA, Park LS. The human pseudoautosomal GM-CSF receptor alpha subunit gene is autosomal in mouse. Nature Genetics. 1: 333-6. PMID 1363815 DOI: 10.1038/Ng0892-333 |
0.467 |
|
| 1993 |
Cattanach BM, Barr JA, Evans EP, Burtenshaw M, Beechey CV, Leff SE, Brannan CI, Copeland NG, Jenkins NA, Jones J. A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression. Nature Genetics. 2: 270-4. PMID 1303278 DOI: 10.1038/Ng1292-270 |
0.544 |
|
| 1992 |
Foroni L, Boehm T, White L, Forster A, Sherrington P, Liao XB, Brannan CI, Jenkins NA, Copeland NG, Rabbitts TH. The rhombotin gene family encode related LIM-domain proteins whose differing expression suggests multiple roles in mouse development. Journal of Molecular Biology. 226: 747-61. PMID 1507224 DOI: 10.1016/0022-2836(92)90630-3 |
0.508 |
|
| 1992 |
Brannan CI, Bedell MA, Resnick JL, Eppig JJ, Handel MA, Williams DE, Lyman SD, Donovan PJ, Jenkins NA, Copeland NG. Developmental abnormalities in Steel17H mice result from a splicing defect in the steel factor cytoplasmic tail Genes and Development. 6: 1832-1842. PMID 1383087 DOI: 10.1101/Gad.6.10.1832 |
0.403 |
|
| 1992 |
Watanabe-Fukunaga R, Brannan CI, Copeland NG, Jenkins NA, Nagata S. Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis. Nature. 356: 314-7. PMID 1372394 DOI: 10.1038/356314A0 |
0.361 |
|
| 1992 |
Brannan CI, Gilbert DJ, Ceci JD, Matsuda Y, Chapman VM, Mercer JA, Eisen H, Johnston LA, Copeland NG, Jenkins NA. An interspecific linkage map of mouse chromosome 15 positioned with respect to the centromere. Genomics. 13: 1075-81. PMID 1354638 DOI: 10.1016/0888-7543(92)90021-J |
0.459 |
|
| 1992 |
Leff SE, Brannan CI, Reed ML, Ozçelik T, Francke U, Copeland NG, Jenkins NA. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nature Genetics. 2: 259-64. PMID 1303276 DOI: 10.1038/Ng1292-259 |
0.537 |
|
| 1991 |
Dolci S, Williams DE, Ernst MK, Resnick JL, Brannan CI, Lock LF, Lyman SD, Boswell HS, Donovan PJ. Requirement for mast cell growth factor for primordial germ cell survival in culture. Nature. 352: 809-11. PMID 1715518 DOI: 10.1038/352809A0 |
0.354 |
|
| 1991 |
Brannan CI, Lyman SD, Williams DE, Eisenman J, Anderson DM, Cosman D, Bedell MA, Jenkins NA, Copeland NG. Steel-Dickie mutation encodes a c-kit ligand lacking transmembrane and cytoplasmic domains. Proceedings of the National Academy of Sciences of the United States of America. 88: 4671-4. PMID 1711207 DOI: 10.1073/Pnas.88.11.4671 |
0.368 |
|
| 1991 |
Goodwin RG, Anderson D, Jerzy R, Davis T, Brannan CI, Copeland NG, Jenkins NA, Smith CA. Molecular cloning and expression of the type 1 and type 2 murine receptors for tumor necrosis factor. Molecular and Cellular Biology. 11: 3020-6. PMID 1645445 DOI: 10.1128/Mcb.11.6.3020 |
0.32 |
|
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