17 results for author:"Galili N." in Literature citations
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| Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes. Bejar R., Stevenson K.E., Caughey B.A., Abdel-Wahab O., Steensma D.P., Galili N., Raza A., Kantarjian H., Levine R.L., Neuberg D. et al. J. Clin. Oncol. 30:3376-3382(2012) · Mapped (9) |
| Coordinate loss of a microRNA and protein-coding gene cooperate in the pathogenesis of 5q- syndrome. Kumar M.S., Narla A., Nonami A., Mullally A., Dimitrova N., Ball B., McAuley J.R., Poveromo L., Kutok J.L., Galili N. et al. Blood 118:4666-4673(2011) · Mapped (2) |
| Identification of RPS14 as a 5q- syndrome gene by RNA interference screen. Ebert B.L., Pretz J., Bosco J., Chang C.Y., Tamayo P., Galili N., Raza A., Root D.E., Attar E., Ellis S.R. et al. Nature 451:335-339(2008) · Mapped (2) |
| Increased levels and activity of E2F1 transcription factor in myelodysplastic bone marrow. Saberwal G., Lucas S., Janssen I., Deobhakta A., Hu W.Y., Galili N., Raza A., Mundle S.D. Int. J. Hematol. 80:146-154(2004) · Mapped (2) |
| Rnf4, a RING protein expressed in the developing nervous and reproductive systems, interacts with Gscl, a gene within the DiGeorge critical region. Galili N., Nayak S., Epstein J.A., Buck C.A. |
| Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2. Lund J., Roe B., Chen F., Budarf M., Galili N., Riblet R., Miller R.D., Emanuel B.S., Reeves R.H. Mamm. Genome 10:438-443(1999) · Mapped (127) |
| Immunohistochemical analysis of the expression of two serine-threonine kinases in the maturing mouse testis. Nayak S., Galili N., Buck C.A. Mech. Dev. 74:171-174(1998) · UniProtKB (2) |
| Gscl, a gene within the minimal DiGeorge critical region, is expressed in primordial germ cells and the developing pons. Galili N., Epstein J.A., Leconte I., Nayak S., Buck C.A. Dev. Dyn. 212:86-93(1998) · Mapped (41) |
| No title Galili N., Baldwin H.S., Lund J., Reeves R., Gong W., Wang Z., Roe B.A., Emanuel B.S., Nayak S., Mickanin C. et al. Genome Res. 7:399-399(1997) |
| Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region. Gong W., Emanuel B.S., Galili N., Kim D.H., Roe B.A., Driscoll D.A., Budarf M.L. Hum. Mol. Genet. 6:267-276(1997) · UniProtKB (1) · Mapped (3) |
| A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region. Galili N., Baldwin H.S., Lund J., Reeves R., Gong W., Wang Z., Roe B.A., Emanuel B.S., Nayak S., Mickanin C. et al. |
| Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma. Galili N., Davis R.J., Fredericks W.J., Mukhopadhyay S., Rauscher F.J. III, Emanuel B.S., Rovera G., Barr F.G. Nat. Genet. 5:230-235(1993) · UniProtKB (3) |
| Genomic organization of the human PAX3 gene: DNA sequence analysis of the region disrupted in alveolar rhabdomyosarcoma. Macina R.A., Barr F.G., Galili N., Riethman H.C. Genomics 26:1-8(1995) · UniProtKB (1) |
| Continuing rearrangement but absence of somatic hypermutation in immunoglobulin genes of human B cell precursor leukemia. Bird J., Galili N., Link M., Stites D., Sklar J. J. Exp. Med. 168:229-245(1988) · UniProtKB (2) |
| Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor. Nourse J., Mellentin J.D., Galili N., Wilkinson J., Stanbridge E., Smith S.D., Cleary M.L. Cell 60:535-545(1990) · UniProtKB (1) |
| PBX2 and PBX3, new homeobox genes with extensive homology to the human proto-oncogene PBX1. Monica K., Galili N., Nourse J., Saltman D., Cleary M.L. Mol. Cell. Biol. 11:6149-6157(1991) · UniProtKB (3) · Mapped (24) |
| The t(1;19)(q23;p13) results in consistent fusion of E2A and PBX1 coding sequences in acute lymphoblastic leukemias. Hunger S.P., Galili N., Carroll A.J., Crist W.M., Link M.P., Cleary M.L. Blood 77:687-693(1991) · UniProtKB (2) |