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H O Sweet

Showing results (21-30 of 30) with videos related to

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Genes & Development|February 15, 1994
Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (a(t)) and white-bellied agouti (Aw) reveals alternative forms of agouti transcriptsS J Bultman, M L Klebig, E J Michaud, et al.
Human Molecular Genetics|June 13, 1998
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactylyK R Johnson, H O Sweet, L R Donahue, et al.
The Journal of Endocrinology|April 1, 1994
Adrenocortical dysplasia: a mouse model system for adrenocortical insufficiencyW G Beamer, H O Sweet, R T Bronson, et al.
Immunogenetics|January 1, 1989
The mouse mutation severe combined immune deficiency (scid) is on chromosome 16G C Bosma, M T Davisson, N R Ruetsch, et al.
Genes & Development|June 15, 1994
Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineageE J Michaud, M J van Vugt, S J Bultman, et al.
British Journal of Haematology|July 1, 1988
Cocoa: a new mouse model for platelet storage pool deficiencyE K Novak, H O Sweet, M Prochazka, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 14, 1997
Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelinD Goldowitz, R C Cushing, E Laywell, et al.
The Journal of Biological Chemistry|May 15, 1989
The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activitiesC A Langner, E H Birkenmeier, O Ben-Zeev, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfectaS D Chipman, H O Sweet, D J McBride, et al.
Genetics|May 3, 2000
Genomic, transcriptional and mutational analysis of the mouse microphthalmia locusJ H Hallsson, J Favor, C Hodgkinson, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Genes & Development|February 15, 1994
Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (a(t)) and white-bellied agouti (Aw) reveals alternative forms of agouti transcriptsS J Bultman, M L Klebig, E J Michaud, et al.
Human Molecular Genetics|June 13, 1998
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactylyK R Johnson, H O Sweet, L R Donahue, et al.
The Journal of Endocrinology|April 1, 1994
Adrenocortical dysplasia: a mouse model system for adrenocortical insufficiencyW G Beamer, H O Sweet, R T Bronson, et al.
Immunogenetics|January 1, 1989
The mouse mutation severe combined immune deficiency (scid) is on chromosome 16G C Bosma, M T Davisson, N R Ruetsch, et al.
Genes & Development|June 15, 1994
Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineageE J Michaud, M J van Vugt, S J Bultman, et al.
British Journal of Haematology|July 1, 1988
Cocoa: a new mouse model for platelet storage pool deficiencyE K Novak, H O Sweet, M Prochazka, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 14, 1997
Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelinD Goldowitz, R C Cushing, E Laywell, et al.
The Journal of Biological Chemistry|May 15, 1989
The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activitiesC A Langner, E H Birkenmeier, O Ben-Zeev, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfectaS D Chipman, H O Sweet, D J McBride, et al.
Genetics|May 3, 2000
Genomic, transcriptional and mutational analysis of the mouse microphthalmia locusJ H Hallsson, J Favor, C Hodgkinson, et al.
Pageof 3