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D L Nelson
S T Warren

Nature genetics

Showing results (1-10 of 15) with videos related to

Pageof 2
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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.
Nature Genetics|July 1, 1993
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeatC T Ashley, J S Sutcliffe, C B Kunst, et al.
Nature Genetics|May 1, 1997
Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeatsK Small, J Iber, S T Warren
Nature Genetics|May 13, 1999
Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cellsB Coffee, F Zhang, S T Warren, et al.
Nature Genetics|May 1, 1996
Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG islandY Gu, Y Shen, R A Gibbs, et al.
Nature Genetics|August 1, 1995
Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndromeK A Lugenbeel, A M Peier, N L Carson, et al.
Nature Genetics|November 1, 1992
Human genes containing polymorphic trinucleotide repeatsG J Riggins, L K Lokey, J L Chastain, et al.
Nature Genetics|February 1, 1997
Characterization of the full fragile X syndrome mutation in fetal gametesH E Malter, J C Iber, R Willemsen, et al.
Nature Genetics|November 1, 1994
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXEJ E Parrish, B A Oostra, A J Verkerk, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
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.
Nature Genetics|July 1, 1993
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeatC T Ashley, J S Sutcliffe, C B Kunst, et al.
Nature Genetics|May 1, 1997
Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeatsK Small, J Iber, S T Warren
Nature Genetics|May 13, 1999
Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cellsB Coffee, F Zhang, S T Warren, et al.
Nature Genetics|May 1, 1996
Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG islandY Gu, Y Shen, R A Gibbs, et al.
Nature Genetics|August 1, 1995
Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndromeK A Lugenbeel, A M Peier, N L Carson, et al.
Nature Genetics|November 1, 1992
Human genes containing polymorphic trinucleotide repeatsG J Riggins, L K Lokey, J L Chastain, et al.
Nature Genetics|February 1, 1997
Characterization of the full fragile X syndrome mutation in fetal gametesH E Malter, J C Iber, R Willemsen, et al.
Nature Genetics|November 1, 1994
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXEJ E Parrish, B A Oostra, A J Verkerk, et al.
Pageof 2