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Annals of Human Genetics
|
March 24, 1999
Susceptibility to spina bifida; an association study of five candidate genes
K Morrison, C Papapetrou, F A Hol, et al.
Genomics
|
September 1, 1996
Glomerular-specific imprinting of the mouse gsalpha gene: how does this relate to hormone resistance in albright hereditary osteodystrophy?
C M Williamson, J Schofield, E R Dutton, et al.
Somatic Cell and Molecular Genetics
|
March 1, 1987
Regional localization of carbonic anhydrase genes CA1 and CA3 on human chromosome 8
M B Davis, L F West, J H Barlow, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1987
Nucleotide and amino acid sequences of human intestinal alkaline phosphatase: close homology to placental alkaline phosphatase
P S Henthorn, M Raducha, Y H Edwards, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes
|
September 21, 2000
An apparent interlocus gene conversion-like event at a putative tumor suppressor gene locus on human chromosome 6q27 in a Burkitt's lymphoma cell line
R S Hauptschein, G Gaidano, P H Rao, et al.
Human Molecular Genetics
|
August 1, 1994
Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell lines
J N Schofield, D J Blake, C Simmons, et al.
Experimental Cell Research
|
December 10, 1999
Forced MyHCIIB expression following targeted genetic manipulation of conditionally immortalized muscle precursor cells
J M Harris, J E Morgan, J D Rosenblatt, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1992
Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1
D B Whitehouse, W Putt, J U Lovegrove, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 1, 1993
A cosmid library specific for human chromosome regions 6p21.3 and 6q27
V P Shortle, P Malaspina, M Fox, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 15, 1993
The classical human phosphoglucomutase (PGM1) isozyme polymorphism is generated by intragenic recombination
R E March, W Putt, M Hollyoake, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 98) with videos related to
Sort By:
Page
of 10
Annals of Human Genetics
|
March 24, 1999
Susceptibility to spina bifida; an association study of five candidate genes
K Morrison, C Papapetrou, F A Hol, et al.
Genomics
|
September 1, 1996
Glomerular-specific imprinting of the mouse gsalpha gene: how does this relate to hormone resistance in albright hereditary osteodystrophy?
C M Williamson, J Schofield, E R Dutton, et al.
Somatic Cell and Molecular Genetics
|
March 1, 1987
Regional localization of carbonic anhydrase genes CA1 and CA3 on human chromosome 8
M B Davis, L F West, J H Barlow, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1987
Nucleotide and amino acid sequences of human intestinal alkaline phosphatase: close homology to placental alkaline phosphatase
P S Henthorn, M Raducha, Y H Edwards, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes
|
September 21, 2000
An apparent interlocus gene conversion-like event at a putative tumor suppressor gene locus on human chromosome 6q27 in a Burkitt's lymphoma cell line
R S Hauptschein, G Gaidano, P H Rao, et al.
Human Molecular Genetics
|
August 1, 1994
Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell lines
J N Schofield, D J Blake, C Simmons, et al.
Experimental Cell Research
|
December 10, 1999
Forced MyHCIIB expression following targeted genetic manipulation of conditionally immortalized muscle precursor cells
J M Harris, J E Morgan, J D Rosenblatt, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1992
Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1
D B Whitehouse, W Putt, J U Lovegrove, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 1, 1993
A cosmid library specific for human chromosome regions 6p21.3 and 6q27
V P Shortle, P Malaspina, M Fox, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 15, 1993
The classical human phosphoglucomutase (PGM1) isozyme polymorphism is generated by intragenic recombination
R E March, W Putt, M Hollyoake, et al.
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of 10