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S T Warren

Showing results (71-80 of 108) with videos related to

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Cell|November 24, 2001
Fragile X mental retardation protein targets G quartet mRNAs important for neuronal functionJ C Darnell, K B Jensen, P Jin, et al.
Science (New York, N.Y.)|May 5, 1995
Translational suppression by trinucleotide repeat expansion at FMR1Y Feng, F Zhang, L K Lokey, et al.
Genes, Chromosomes & Cancer|February 1, 1994
CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosomeG J Riggins, S L Sherman, C N Phillips, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakageS T Warren, S J Knight, J F Peters, et al.
Human Molecular Genetics|September 1, 1992
DNA methylation represses FMR-1 transcription in fragile X syndromeJ S Sutcliffe, D L Nelson, F Zhang, et al.
Cancer Research|December 5, 2000
TMS1, a novel proapoptotic caspase recruitment domain protein, is a target of methylation-induced gene silencing in human breast cancersK E Conway, B B McConnell, C E Bowring, et al.
American Journal of Medical Genetics|August 9, 1996
A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 geneA M Lachiewicz, G A Spiridigliozzi, A McConkie-Rosell, et al.
Nature Genetics|January 1, 1993
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndromeH L Hinds, C T Ashley, J S Sutcliffe, et al.
Nature Genetics|November 1, 1995
Evolution of the cryptic FMR1 CGG repeatE E Eichler, C B Kunst, K A Lugenbeel, et al.
Cell|August 23, 1991
Absence of expression of the FMR-1 gene in fragile X syndromeM Pieretti, F P Zhang, Y H Fu, et al.
Pageof 11

Showing results (71-80 of 108) with videos related to

Sort By:
Pageof 11
Cell|November 24, 2001
Fragile X mental retardation protein targets G quartet mRNAs important for neuronal functionJ C Darnell, K B Jensen, P Jin, et al.
Science (New York, N.Y.)|May 5, 1995
Translational suppression by trinucleotide repeat expansion at FMR1Y Feng, F Zhang, L K Lokey, et al.
Genes, Chromosomes & Cancer|February 1, 1994
CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosomeG J Riggins, S L Sherman, C N Phillips, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakageS T Warren, S J Knight, J F Peters, et al.
Human Molecular Genetics|September 1, 1992
DNA methylation represses FMR-1 transcription in fragile X syndromeJ S Sutcliffe, D L Nelson, F Zhang, et al.
Cancer Research|December 5, 2000
TMS1, a novel proapoptotic caspase recruitment domain protein, is a target of methylation-induced gene silencing in human breast cancersK E Conway, B B McConnell, C E Bowring, et al.
American Journal of Medical Genetics|August 9, 1996
A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 geneA M Lachiewicz, G A Spiridigliozzi, A McConkie-Rosell, et al.
Nature Genetics|January 1, 1993
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndromeH L Hinds, C T Ashley, J S Sutcliffe, et al.
Nature Genetics|November 1, 1995
Evolution of the cryptic FMR1 CGG repeatE E Eichler, C B Kunst, K A Lugenbeel, et al.
Cell|August 23, 1991
Absence of expression of the FMR-1 gene in fragile X syndromeM Pieretti, F P Zhang, Y H Fu, et al.
Pageof 11