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Results: 1-10 |
Results: 10
Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1
Authors: Costa, RM Yang, T Huynh, DP Pulst, SM Viskochil, DH Silva, AJ Brannan, CI
Citation: Rm. Costa et al., Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1, NAT GENET, 27(4), 2001, pp. 399-405
Maternal methylation imprints on human chromosome 15 are established during or after fertilization
Authors: 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
Citation: O. El-maarri et al., Maternal methylation imprints on human chromosome 15 are established during or after fertilization, NAT GENET, 27(3), 2001, pp. 341-344
Autosomal telomere exchange results in the rapid amplification and dispersion of Csf2ra genes in wild-derived mice
Authors: Brannan, CI Disteche, CM Park, LS Copeland, NG Jenkins, NA
Citation: Ci. Brannan et al., Autosomal telomere exchange results in the rapid amplification and dispersion of Csf2ra genes in wild-derived mice, MAMM GENOME, 12(12), 2001, pp. 882-886
The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a
Authors: Chamberlain, SJ Brannan, CI
Citation: Sj. Chamberlain et Ci. Brannan, The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a, GENOMICS, 73(3), 2001, pp. 316-322
Retroviral integration at the Epi1 locus cooperates with Nf1 gene loss in the progression to acute myeloid leukemia
Authors: Blaydes, SM Kogan, SC Truong, BTH Gilbert, DJ Jenkins, NA Copeland, NG Largaespada, DA Brannan, CI
Citation: Sm. Blaydes et al., Retroviral integration at the Epi1 locus cooperates with Nf1 gene loss in the progression to acute myeloid leukemia, J VIROLOGY, 75(19), 2001, pp. 9427-9434
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
Authors: Bielinska, B Blaydes, SM Buiting, K Yang, T Krajewska-Walasek, M Horsthemke, B Brannan, CI
Citation: B. Bielinska et al., De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch, NAT GENET, 25(1), 2000, pp. 74-78
Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype
Authors: Lee, S Kozlov, S Hernandez, L Chamberlain, SJ Brannan, CI Stewart, CL Wevrick, R
Citation: S. Lee et al., Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype, HUM MOL GEN, 9(12), 2000, pp. 1813-1819
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
Authors: Cavaille, J Buiting, K Kiefmann, M Lalande, M Brannan, CI Horsthemke, B Bachellerie, JP Brosius, J Huttenhofer, A
Citation: J. Cavaille et al., Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization, P NAS US, 97(26), 2000, pp. 14311-14316
Mechanisms of genomic imprinting
Authors: Brannan, CI Bartolomei, MS
Citation: Ci. Brannan et Ms. Bartolomei, Mechanisms of genomic imprinting, CUR OP GEN, 9(2), 1999, pp. 164-170
Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice
Authors: Blaydes, SM Elmore, M Yang, T Brannan, CI
Citation: Sm. Blaydes et al., Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice, MAMM GENOME, 10(6), 1999, pp. 549-555
Risultati: 1-10 |