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Genetics
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May 1, 1996
Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex
T P O'Brien, D L Metallinos, H Chen, et al.
Genetics
|
October 1, 1995
Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome
R J Oakey, P G Matteson, S Litwin, et al.
Science (New York, N.Y.)
|
January 2, 1987
Diversity of alpha-fetoprotein gene expression in mice is generated by a combination of separate enhancer elements
R E Hammer, R Krumlauf, S A Camper, et al.
Genetics
|
October 23, 1997
Two dominant mutations in the mouse fused gene are the result of transposon insertions
T J Vasicek, L Zeng, X J Guan, et al.
Genes & Development
|
September 1, 1995
An enhancer deletion affects both H19 and Igf2 expression
P A Leighton, J R Saam, R S Ingram, et al.
The Journal of Biological Chemistry
|
February 25, 1981
The evolution of alpha-fetoprotein and albumin. I. A comparison of the primary amino acid sequences of mammalian alpha-fetoprotein and albumin
M B Gorin, D L Cooper, F Eiferman, et al.
Genes & Development
|
August 19, 2000
The Dlk1 and Gtl2 genes are linked and reciprocally imprinted
J V Schmidt, P G Matteson, B K Jones, et al.
Genomics
|
November 5, 1997
Structure and expression of the mouse L23mrp gene downstream of the imprinted H19 gene: biallelic expression and lack of interaction with the H19 enhancers
M Zubair, K Hilton, J R Saam, et al.
Nature Genetics
|
April 1, 1995
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
K D Tremblay, J R Saam, R S Ingram, et al.
Nature Genetics
|
August 31, 2001
Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice
M A Cleary, C D van Raamsdonk, J Levorse, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 98) with videos related to
Sort By:
Page
of 10
Genetics
|
May 1, 1996
Complementation mapping of skeletal and central nervous system abnormalities in mice of the piebald deletion complex
T P O'Brien, D L Metallinos, H Chen, et al.
Genetics
|
October 1, 1995
Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome
R J Oakey, P G Matteson, S Litwin, et al.
Science (New York, N.Y.)
|
January 2, 1987
Diversity of alpha-fetoprotein gene expression in mice is generated by a combination of separate enhancer elements
R E Hammer, R Krumlauf, S A Camper, et al.
Genetics
|
October 23, 1997
Two dominant mutations in the mouse fused gene are the result of transposon insertions
T J Vasicek, L Zeng, X J Guan, et al.
Genes & Development
|
September 1, 1995
An enhancer deletion affects both H19 and Igf2 expression
P A Leighton, J R Saam, R S Ingram, et al.
The Journal of Biological Chemistry
|
February 25, 1981
The evolution of alpha-fetoprotein and albumin. I. A comparison of the primary amino acid sequences of mammalian alpha-fetoprotein and albumin
M B Gorin, D L Cooper, F Eiferman, et al.
Genes & Development
|
August 19, 2000
The Dlk1 and Gtl2 genes are linked and reciprocally imprinted
J V Schmidt, P G Matteson, B K Jones, et al.
Genomics
|
November 5, 1997
Structure and expression of the mouse L23mrp gene downstream of the imprinted H19 gene: biallelic expression and lack of interaction with the H19 enhancers
M Zubair, K Hilton, J R Saam, et al.
Nature Genetics
|
April 1, 1995
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
K D Tremblay, J R Saam, R S Ingram, et al.
Nature Genetics
|
August 31, 2001
Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice
M A Cleary, C D van Raamsdonk, J Levorse, et al.
Page
of 10