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Results: 1-12 |
Results: 12
Genomic organisation of the mouse Ret proto-oncogene
Authors: Panetta, D Yin, L Barale, R Romeo, G Ravazzolo, R Ceccherini, I Puliti, A
Citation: D. Panetta et al., Genomic organisation of the mouse Ret proto-oncogene, DNA SEQ, 11(6), 2001, pp. 501-506
Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4-A5 by in situ hybridization
Authors: Cinti, R Fava, M Sancandi, M Matera, I Ravazzolo, R Ceccherini, I
Citation: R. Cinti et al., Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4-A5 by in situ hybridization, CYTOG C GEN, 92(3-4), 2001, pp. 354-355
The sensitivity of activated Cys Ret mutants to glial cell line-derived neurotrophic factor is mandatory to rescue neuroectodermic cells from apoptosis
Authors: Mograbi, B Bocciardi, R Bourget, I Juhel, T Farahi-Far, D Romeo, G Ceccherini, I Rossi, B
Citation: B. Mograbi et al., The sensitivity of activated Cys Ret mutants to glial cell line-derived neurotrophic factor is mandatory to rescue neuroectodermic cells from apoptosis, MOL CELL B, 21(20), 2001, pp. 6719-6730
A heterozygous endothelin 3 mutation in Waardenburg-Hirschsprung disease: is there a dosage effect of EDN3/EDNRB gene mutations on neurocristopathy phenotypes?
Authors: Pingault, V Bondurand, N Lemort, N Sancandi, M Ceccherini, I Hugot, JP Jouk, PS Goossens, M
Citation: V. Pingault et al., A heterozygous endothelin 3 mutation in Waardenburg-Hirschsprung disease: is there a dosage effect of EDN3/EDNRB gene mutations on neurocristopathy phenotypes?, J MED GENET, 38(3), 2001, pp. 205-208
cDNA sequence and genomic structure of the rat RET proto-oncogene
Authors: Matera, I Miguel-Rodriguez, MD Fernandez-Santos, JM Santamaria, G Puliti, A Ravazzolo, R Romeo, G Galera-Davidson, H Ceccherini, I
Citation: I. Matera et al., cDNA sequence and genomic structure of the rat RET proto-oncogene, DNA SEQ, 11(5), 2000, pp. 405-417
A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease
Authors: Griseri, P Sancandi, M Patrone, G Bocciardi, R Hofstra, R Ravazzolo, R Devoto, M Romeo, G Ceccherini, I
Citation: P. Griseri et al., A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease, EUR J HUM G, 8(9), 2000, pp. 721-724
Nuclear run-on assay using biotin labeling, magnetic bead capture and analysis by fluorescence-based RT-PCR
Authors: Patrone, G Puppo, F Cusano, R Scaranari, M Ceccherini, I Puliti, A Ravazzolo, R
Citation: G. Patrone et al., Nuclear run-on assay using biotin labeling, magnetic bead capture and analysis by fluorescence-based RT-PCR, BIOTECHNIQU, 29(5), 2000, pp. 1012
Pathogenesis of Hirschsprung's disease
Authors: Martucciello, G Ceccherini, I Lerone, M Jasonni, V
Citation: G. Martucciello et al., Pathogenesis of Hirschsprung's disease, J PED SURG, 35(7), 2000, pp. 1017-1025
Incidence of RET mutations in patients with Hirschsprung's disease
Authors: Sancandi, M Ceccherini, I Costa, M Fava, M Chen, B Wu, Y Hofstra, R Laurie, T Griffths, M Burge, D Tam, PKH
Citation: M. Sancandi et al., Incidence of RET mutations in patients with Hirschsprung's disease, J PED SURG, 35(1), 2000, pp. 139-142
HOX11L1, a gene involved in peripheral nervous system development, maps tohuman chromosome 2p13.1 -> p12 and mouse chromosome 6C3-D1
Authors: Puliti, A Cinti, R Betsos, N Romeo, G Ceccherini, I
Citation: A. Puliti et al., HOX11L1, a gene involved in peripheral nervous system development, maps tohuman chromosome 2p13.1 -> p12 and mouse chromosome 6C3-D1, CYTOG C GEN, 84(1-2), 1999, pp. 115-117
Double heterozygosity for a RET substitution interfering with splicing andan EDNRB missense mutation in Hirschsprung disease
Authors: Auricchio, A Griseri, P Carpentieri, ML Betsos, N Staiano, A Tozzi, A Priolo, M Thompson, H Bocciardi, R Romeo, G Ballabio, A Ceccherini, I
Citation: A. Auricchio et al., Double heterozygosity for a RET substitution interfering with splicing andan EDNRB missense mutation in Hirschsprung disease, AM J HU GEN, 64(4), 1999, pp. 1216-1221
Physical mapping of the short arm of human chromosome 16
Authors: Mole, SE Breuning, MH Ceccherini, I Harris, PC Lushnikova, T
Citation: Se. Mole et al., Physical mapping of the short arm of human chromosome 16, BIOM HLTH R, 23, 1998, pp. 129-149
Risultati: 1-12 |