The Prader–Willi Syndrome Imprinting Center Activates the Paternally Expressed Murine Ube3a Antisense Transcript but Represses Paternal Ube3a von Chamberlain, Stormy J., Brannan, Camilynn I.

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Maternal methylation imprints on human chromosome 15 are established during or after fertilization von Walter, Jörn, El-Maarri, Osman, Buiting, Karin, Peery, Edwin G, Kroisel, Peter M, Balaban, Basak, Wagner, Klaus, Urman, Bulent, Heyd, Julia, Lich, Christina, Brannan, Camilynn I, Horsthemke, Bernhard

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Pillars article: lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis. 1992 von Watanabe-Fukunaga, Rie, Brannan, Camilynn I, Copeland, Neal G, Jenkins, Nancy A, Nagata, Shigekazu

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De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch von Horsthemke, Bernhard, Bielinska, Beata, Blaydes, Susan M, Buiting, Karin, Yang, Tao, Krajewska-Walasek, Malgorzata, Brannan, Camilynn I

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A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects von Johnstone, Karen A., DuBose, Amanda J., Futtner, Christopher R., Elmore, Michael D., Brannan, Camilynn I., Resnick, James L.

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Identification of Brain-Specific and Imprinted Small Nucleolar RNA Genes Exhibiting an Unusual Genomic Organization von Cavaillé, J, Buiting, K, Kiefmann, M, Lalande, M, Brannan, C I, Horsthemke, B, Bachellerie, J P, Brosius, J, Hüttenhofer, A

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Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1 von Huynh, Duong P, Brannan, Camilynn I, Costa, Rui M, Yang, Tao, Viskochil, David H, Pulst, Stefan M, Silva, Alcino J

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Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis von Watanabe-Fukunaga, Rie, Brannan, Camilynn I, Copeland, Neal G, Jenkins, Nancy A, Nagata, Shigekazu

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A mouse model for Prader-Willi syndrome imprinting-centre mutations von Yang, Tao, Adamson, Todd E, Resnick, James L, Leff, Stuart, Wevrick, Rachel, Francke, Uta, Jenkins, Nancy A, Copeland, Neal G, Brannan, Camilynn I

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Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype von LEE, S, KOZLOV, S, HERNANDEZ, L, CHAMBERLAIN, S. J, BRANNAN, C. I, STEWART, C. L, WEVRICK, R

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Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice von Chamberlain, Stormy J., Johnstone, Karen A., DuBose, Amanda J., Simon, Thomas A., Bartolomei, Marisa S., Resnick, James L., Brannan, Camilynn I.

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Mechanisms of genomic imprinting von Brannan, Camilynn I, Bartolomei, Marisa S

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Requirement for mast cell growth factor for primordial germ cell survival in culture von Dolci, Susanna, Williams, Douglas E, Ernst, Mary K, Resnick, James L, Brannan, Camilynn I, Lock, Leslie F, Lyman, Stewart D, Boswell, H. Scott, Donovan, Peter J

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Loss of neurofibromin results in neurotrophin-independent survival of embryonic sensory and sympathetic neurons von Vogel, Kristine S, Brannan, Camilynn I, Jenkins, Nancy A, Copeland, Neal G, Parada, Luis F

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targeted deletion upstream of Snrpn does not result in an imprinting defect von Peery, Edwin G, Elmore, Michael D, Resnick, James L, Brannan, Camilynn I, Johnstone, Karen A

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Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region von Leff, Stuart E, Brannan, Camilynn I, Reed, Martha L, Özçelik, Tayfun, Francke, Uta, Copeland, Neal G, Jenkins, Nancy A

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Neurofibromin Expression and Astrogliosis in Neurofibromatosis (Type 1) Brains von NORDLUND, MICHAEL L, RIZVI, TILAT A, BRANNAN, CAMILYNN I, RATNER, NANCY

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A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression von Cattanach, Bruce M, Barr, Jacqueline A, Evans, Edward P, Burtenshaw, Michael, Beechey, Colin V, Leff, Stuart E, Brannan, Camilynn I, Copeland, Neal G, Jenkins, Nancy A, Jones, Janet

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Pillars Article: Lymphoproliferation Disorder in Mice Explained by Defects in Fas Antigen that MediatesApoptosis. Nature. 1992. 356: 314-317 von Watanabe-Fukunaga, Rie, Brannan, Camilynn I, Copeland, Neal G, Jenkins, Nancy A, Nagata, Shigekazu

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Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice von Blaydes, Susan M, Elmore, Michael, Yang, Tao, Brannan, Camilynn I

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