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Neuromuscular Disorders : NMD|July 23, 1998
Immunocytochemical detection of emerin within the nuclear matrixS Squarzoni, P Sabatelli, A Ognibene, et al.
Molecular and Cellular Biology|July 1, 1988
Processing, secretion, and biological properties of a novel growth factor of the fibroblast growth factor family with oncogenic potentialP Delli-Bovi, A M Curatola, K M Newman, et al.
American Journal of Human Genetics|January 1, 1992
Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivationE Maestrini, S Rivella, C Tribioli, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1984
Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this siteP Szabo, M Purrello, M Rocchi, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 23, 1996
An X chromosome-linked gene encoding a protein with characteristics of a rhoGAP predominantly expressed in hematopoietic cellsC Tribioli, S Droetto, S Bione, et al.
Human Molecular Genetics|July 1, 1992
An archipelago of CpG islands in Xq28: identification and fine mapping of 20 new CpG islands of the human X chromosomeE Maestrini, F Tamanini, P Kioschis, et al.
The American Journal of Pathology|November 12, 1998
Targeted disruption of the FGF2 gene does not prevent choroidal neovascularization in a murine modelT Tobe, S Ortega, J D Luna, et al.
The Journal of Clinical Investigation|March 1, 1993
Expression of int-2 oncogene in Kaposi's sarcoma lesionsY Q Huang, J J Li, D Moscatelli, et al.
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|February 1, 1990
Autocrine growth stimulation by secreted Kaposi fibroblast growth factor but not by endogenous basic fibroblast growth factorA Wellstein, R Lupu, G Zugmaier, et al.
American Journal of Human Genetics|September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in malesI Meloni, M Bruttini, I Longo, et al.
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