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Brain Research Bulletin|November 24, 2001
The Fragile X mental retardation proteinB Bardoni, A Schenck, J L MandelHuman Molecular Genetics|November 11, 1999
A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) proteinB Bardoni, A Schenck, J L MandelAmerican Journal of Medical Genetics|February 17, 2001
FMR1 gene and fragile X syndromeB Bardoni, J L Mandel, G S FischJournal of Medical Genetics|November 10, 2000
Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?U Salat, B Bardoni, D Wöhrle, et al.Neurobiology of Disease|January 1, 1997
Analysis of domains affecting intracellular localization of the FMRP proteinB Bardoni, A Sittler, Y Shen, et al.Genomics|October 1, 1990
Two families of low-copy-number repeats are interspersed on Xp22.3: implications for the high frequency of deletions in this regionA Ballabio, B Bardoni, S Guioli, et al.Human Genetics|December 1, 1988
A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphismsB Bardoni, S Guioli, E Maserati, et al.Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|May 23, 2001
[Screening of proteins interact with FMR1 by yeast two-hybrid system]Y Chen, A Sittler, M Yu, et al.Proceedings of the National Academy of Sciences of the United States of America|July 5, 2001
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2PA Schenck, B Bardoni, A Moro, et al.European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|December 10, 1999
Is bilateral congenital anorchia genetically determined?G B Parigi, B Bardoni, V Avoltini, et al.Pageof 4