Effect of genetic background on phenotype variability in transgenic mouse models of amyotrophic lateral sclerosis: A window of opportunity in the search for genetic modifiers
Heiman-Patterson, Terry D., Sher, Roger B., Blankenhorn, Elizabeth A., Alexander, Guillermo, Deitch, Jeffrey S., Kunst, Catherine B., Maragakis, Nicholas, Cox, Gregory
Published in Amyotrophic lateral sclerosis (01.03.2011)
Published in Amyotrophic lateral sclerosis (01.03.2011)
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Journal Article
Mutations in SOD1 associated with amyotrophic lateral sclerosis cause novel protein interactions
Kunst, Catherine B, Mezey, Eva, Brownstein, Michael J, Patterson, David
Published in Nature genetics (01.01.1997)
Published in Nature genetics (01.01.1997)
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Journal Article
Genetic Mapping of a Mouse Modifier Gene That Can Prevent ALS Onset
Kunst, Catherine B., Messer, Laurel, Gordon, Jon, Haines, Jonathan, Patterson, David
Published in Genomics (San Diego, Calif.) (01.12.2000)
Published in Genomics (San Diego, Calif.) (01.12.2000)
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Journal Article
Human and murine FMR-1 : alternative splicing and translational initiation downstream of the CGG-repeat
Ashley, Claude T, Sutcliffe, James S, Kunst, Catherine B, Leiner, Harold A, Eichler, Evan E, Nelson, David L, Warren, Stephen T
Published in Nature genetics (01.07.1993)
Published in Nature genetics (01.07.1993)
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Journal Article
Evolution of the cryptic FMR1 CGG repeat
Eichler, Evan E, Kunst, Catherine B, Lugenbeel, Kellie A, Ryder, Oliver A, Davison, Daniel, Warren, Stephen T, Nelson, David L
Published in Nature genetics (01.11.1995)
Published in Nature genetics (01.11.1995)
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Journal Article
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
Verkerk, Annemieke J.M.H., Pieretti, Maura, Sutcliffe, James S., Fu, Ying-Hui, Kuhl, Derek P.A., Pizzuti, Antonio, Reiner, Orly, Richards, Stephen, Victoria, Maureen F., Zhang, Fuping, Eussen, Bert E., van Ommen, Gert-Jan B., Blonden, Lau A.J., Riggins, Gregory J., Chastain, Jane L., Kunst, Catherine B., Galjaard, Hans, Thomas Caskey, C., Nelson, David L., Oostra, Ben A., Warren, Stephen T.
Published in Cell (31.05.1991)
Published in Cell (31.05.1991)
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Journal Article
Re-Examination of Factors Associated with Expansion of CGG Repeats Using a Single Nucleotide Polymorphism in FMR1
Gunter, Chris, Paradee, William, Crawford, Dana C., Meadows, Kellen A., Newman, James, Kunst, Catherine B., Nelson, David L., Schwartz, Charles, Murray, Anna, Macpherson, James N., Sherman, Stephanie L., Warren, Stephen T.
Published in Human molecular genetics (01.11.1998)
Published in Human molecular genetics (01.11.1998)
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Journal Article
FMR1 in global populations
KUNST, C. B, ZERYLNICK, C, KARICKHOFF, L, EICHLER, E, BULLARD, J, CHALIFOUX, M, HOLDEN, J. J. A, TORRONI, A, NELSON, D. L, WARREN, S. T
Published in American journal of human genetics (01.03.1996)
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Published in American journal of human genetics (01.03.1996)
Journal Article
The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing
Kunst, C B, Leeflang, E P, Iber, J C, Arnheim, N, Warren, S T
Published in Journal of medical genetics (01.08.1997)
Published in Journal of medical genetics (01.08.1997)
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Journal Article
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes
van den Ouweland, A M, Deelen, W H, Kunst, C B, Uzielli, M L, Nelson, D L, Warren, S T, Oostra, B A, Halley, D J
Published in Human molecular genetics (01.10.1994)
Published in Human molecular genetics (01.10.1994)
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Actin-Binding Protein (ABP-280) Filamin Gene (FLN) Maps Telomeric to the Color Vision Locus (R/GCP) and Centromeric to G6PD in Xq28
Gorlin, Jed B., Henske, Elizabeth, Warren, Stephen T., Kunst, Catherine B., D'Urso, Michele, Palmieri, Giuseppe, Hartwig, John H., Bruns, Gail, Kwiatkowski, David J.
Published in Genomics (San Diego, Calif.) (01.08.1993)
Published in Genomics (San Diego, Calif.) (01.08.1993)
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