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Items: 4

1.
Phylogenetic Modeling of Heterogeneous Gene-Expression Microarray Data from Cancerous Specimens
Mones S. Abu-Asab, Mohamed Chaouchi, Hakima Amri
OMICS. 2008 Sep; 12(3): 183–199. doi: 10.1089/omi.2008.0010
PMCID:
PMC2583934
AbstractArticlePDF–294K
2.
Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region
Yong-hui Jiang, Kekio Wauki, Qian Liu, Jan Bressler, Yanzhen Pan, Catherine D Kashork, Lisa G Shaffer, Arthur L Beaudet
BMC Genomics. 2008; 9: 50. Published online 2008 Jan 28. doi: 10.1186/1471-2164-9-50
PMCID:
PMC2268926
AbstractArticlePDF–831K
3.
Identification of Four Highly Conserved Genes between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transposition Mediated by Flanking Duplicons
J-H. Chai, D. P. Locke, J. M. Greally, J. H. M. Knoll, T. Ohta, J. Dunai, A. Yavor, E. E. Eichler, R. D. Nicholls
Am J Hum Genet. 2003 Oct; 73(4): 898–925. Published online 2003 Sep 23. doi: 10.1086/378816
PMCID:
PMC1180611
AbstractArticlePDF–1.6M
4.
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P
Annette Schenck, Barbara Bardoni, Annamaria Moro, Claudia Bagni, Jean-Louis Mandel
Proc Natl Acad Sci U S A. 2001 Jul 17; 98(15): 8844–8849. Published online 2001 Jul 3. doi: 10.1073/pnas.151231598
PMCID:
PMC37523
AbstractArticlePDF–531K

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