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Genetics
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August 1, 1993
Mouse models of human phenylketonuria
A Shedlovsky, J D McDonald, D Symula, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
February 1, 1997
A candidate mouse model for Hartnup disorder deficient in neutral amino acid transport
D J Symula, A Shedlovsky, E N Guillery, et al.
Genetical Research
|
April 1, 1986
Induction of recessive lethal mutations in the T/t-H-2 region of the mouse genome by a point mutagen
A Shedlovsky, J L Guenet, L L Johnson, et al.
Molecular and Cellular Biology
|
March 1, 1988
A gene encoding the major beta tubulin of the mitotic spindle in Physarum polycephalum plasmodia
T G Burland, E C Paul, M Oetliker, et al.
Science (New York, N.Y.)
|
December 9, 1977
Genetic structure of the replication origin of bacteriophage lambda
M E Furth, F R Blattner, C McLeester, et al.
Immunogenetics
|
January 1, 1981
Strong teratocarcinoma transplantation loci, Gt-1 and Gt-2, flank H-2
A Shedlovsky, L J Clipson, J L VandeBerg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1990
Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase
J D McDonald, V C Bode, W F Dove, et al.
Progress in Clinical and Biological Research
|
January 1, 1990
The use of N-ethyl-N-nitrosourea to produce mouse models for human phenylketonuria and hyperphenylalaninemia
J D McDonald, V C Bode, W F Dove, et al.
Seminars in Cancer Biology
|
October 1, 1996
Manipulation of the mouse germline in the study of Min-induced neoplasia
A Bilger, A R Shoemaker, K A Gould, et al.
The Journal of Cell Biology
|
March 1, 1992
The Min (multiple intestinal neoplasia) mutation: its effect on gut epithelial cell differentiation and interaction with a modifier system
A R Moser, W F Dove, K A Roth, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 115) with videos related to
Sort By:
Page
of 12
Genetics
|
August 1, 1993
Mouse models of human phenylketonuria
A Shedlovsky, J D McDonald, D Symula, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
February 1, 1997
A candidate mouse model for Hartnup disorder deficient in neutral amino acid transport
D J Symula, A Shedlovsky, E N Guillery, et al.
Genetical Research
|
April 1, 1986
Induction of recessive lethal mutations in the T/t-H-2 region of the mouse genome by a point mutagen
A Shedlovsky, J L Guenet, L L Johnson, et al.
Molecular and Cellular Biology
|
March 1, 1988
A gene encoding the major beta tubulin of the mitotic spindle in Physarum polycephalum plasmodia
T G Burland, E C Paul, M Oetliker, et al.
Science (New York, N.Y.)
|
December 9, 1977
Genetic structure of the replication origin of bacteriophage lambda
M E Furth, F R Blattner, C McLeester, et al.
Immunogenetics
|
January 1, 1981
Strong teratocarcinoma transplantation loci, Gt-1 and Gt-2, flank H-2
A Shedlovsky, L J Clipson, J L VandeBerg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1990
Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase
J D McDonald, V C Bode, W F Dove, et al.
Progress in Clinical and Biological Research
|
January 1, 1990
The use of N-ethyl-N-nitrosourea to produce mouse models for human phenylketonuria and hyperphenylalaninemia
J D McDonald, V C Bode, W F Dove, et al.
Seminars in Cancer Biology
|
October 1, 1996
Manipulation of the mouse germline in the study of Min-induced neoplasia
A Bilger, A R Shoemaker, K A Gould, et al.
The Journal of Cell Biology
|
March 1, 1992
The Min (multiple intestinal neoplasia) mutation: its effect on gut epithelial cell differentiation and interaction with a modifier system
A R Moser, W F Dove, K A Roth, et al.
Page
of 12