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Genomics
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January 1, 1996
The chicken FMR1 gene is highly conserved with a CCT 5'-untranslated repeat and encodes an RNA-binding protein
D K Price, F Zhang, C T Ashley, et al.
Human Molecular Genetics
|
August 1, 1996
The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals
D E Eberhart, H E Malter, Y Feng, et al.
Science (New York, N.Y.)
|
October 22, 1993
FMR1 protein: conserved RNP family domains and selective RNA binding
C T Ashley, K D Wilkinson, D Reines, et al.
Human Genetics
|
December 1, 1988
Molecular evidence for true isochromosome 21q
J H Priest, R D Blackston, L A Pearse, et al.
Genomics
|
March 1, 1990
Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction
S A Ledbetter, D L Nelson, S T Warren, et al.
Human Molecular Genetics
|
October 1, 1993
High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome
I K Hornstra, D L Nelson, S T Warren, et al.
Seminars in Neurology
|
March 11, 2000
Emery-Dreifuss muscular dystrophy
A S Zacharias, M E Wagener, S T Warren, et al.
American Journal of Medical Genetics
|
May 1, 1988
Strategy for molecular cloning of the fragile X site DNA
S T Warren, F P Zhang, J S Sutcliffe, et al.
Somatic Cell and Molecular Genetics
|
September 1, 1984
Isolation and characterization of human factor IX cDNA: identification of Taq I polymorphism and regional assignment
P Jagadeeswaran, D E Lavelle, R Kaul, et al.
Molecular Carcinogenesis
|
January 1, 1989
Potential role of the human Ha-ras oncogene in the inhibition of gap junctional intercellular communication
M H el-Fouly, J E Trosko, C C Chang, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 108) with videos related to
Sort By:
Page
of 11
Genomics
|
January 1, 1996
The chicken FMR1 gene is highly conserved with a CCT 5'-untranslated repeat and encodes an RNA-binding protein
D K Price, F Zhang, C T Ashley, et al.
Human Molecular Genetics
|
August 1, 1996
The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals
D E Eberhart, H E Malter, Y Feng, et al.
Science (New York, N.Y.)
|
October 22, 1993
FMR1 protein: conserved RNP family domains and selective RNA binding
C T Ashley, K D Wilkinson, D Reines, et al.
Human Genetics
|
December 1, 1988
Molecular evidence for true isochromosome 21q
J H Priest, R D Blackston, L A Pearse, et al.
Genomics
|
March 1, 1990
Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction
S A Ledbetter, D L Nelson, S T Warren, et al.
Human Molecular Genetics
|
October 1, 1993
High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome
I K Hornstra, D L Nelson, S T Warren, et al.
Seminars in Neurology
|
March 11, 2000
Emery-Dreifuss muscular dystrophy
A S Zacharias, M E Wagener, S T Warren, et al.
American Journal of Medical Genetics
|
May 1, 1988
Strategy for molecular cloning of the fragile X site DNA
S T Warren, F P Zhang, J S Sutcliffe, et al.
Somatic Cell and Molecular Genetics
|
September 1, 1984
Isolation and characterization of human factor IX cDNA: identification of Taq I polymorphism and regional assignment
P Jagadeeswaran, D E Lavelle, R Kaul, et al.
Molecular Carcinogenesis
|
January 1, 1989
Potential role of the human Ha-ras oncogene in the inhibition of gap junctional intercellular communication
M H el-Fouly, J E Trosko, C C Chang, et al.
Page
of 11