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C B Kunst

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

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Cell|June 17, 1994
Cryptic and polar variation of the fragile X repeat could result in predisposing normal allelesC B Kunst, S T Warren
Nature Genetics|January 1, 1997
Mutations in SOD1 associated with amyotrophic lateral sclerosis cause novel protein interactionsC B Kunst, E Mezey, M J Brownstein, et al.
Genomics|December 9, 2000
Genetic mapping of a mouse modifier gene that can prevent ALS onsetC B Kunst, L Messer, J Gordon, et al.
Journal of Medical Genetics|August 1, 1997
The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typingC B Kunst, E P Leeflang, J C Iber, 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.
Genomics|August 1, 1993
Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28J B Gorlin, E Henske, S T Warren, et al.
American Journal of Human Genetics|March 1, 1996
FMR1 in global populationsC B Kunst, C Zerylnick, L Karickhoff, et al.
Human Molecular Genetics|October 1, 1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomesA M van den Ouweland, W H Deelen, C B Kunst, et al.
Human Molecular Genetics|November 13, 1998
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1C Gunter, W Paradee, D C Crawford, et al.
Pageof 1

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

Sort By:
Pageof 1
Cell|June 17, 1994
Cryptic and polar variation of the fragile X repeat could result in predisposing normal allelesC B Kunst, S T Warren
Nature Genetics|January 1, 1997
Mutations in SOD1 associated with amyotrophic lateral sclerosis cause novel protein interactionsC B Kunst, E Mezey, M J Brownstein, et al.
Genomics|December 9, 2000
Genetic mapping of a mouse modifier gene that can prevent ALS onsetC B Kunst, L Messer, J Gordon, et al.
Journal of Medical Genetics|August 1, 1997
The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typingC B Kunst, E P Leeflang, J C Iber, 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.
Genomics|August 1, 1993
Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28J B Gorlin, E Henske, S T Warren, et al.
American Journal of Human Genetics|March 1, 1996
FMR1 in global populationsC B Kunst, C Zerylnick, L Karickhoff, et al.
Human Molecular Genetics|October 1, 1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomesA M van den Ouweland, W H Deelen, C B Kunst, et al.
Human Molecular Genetics|November 13, 1998
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1C Gunter, W Paradee, D C Crawford, et al.
Pageof 1