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Human Molecular Genetics
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September 1, 1997
Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome
J A Joyce, W K Lam, D J Catchpoole, et al.
Veterinary Pathology
|
September 7, 2010
Training pathologists in mouse pathology
J P Sundberg, J M Ward, H HogenEsch, 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.
Journal of Medical Genetics
|
January 11, 2000
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
J R Engel, A Smallwood, A Harper, et al.
British Journal of Clinical Pharmacology
|
December 23, 1998
Comparison of the vasoconstrictor effects of rizatriptan and sumatriptan in human isolated cranial arteries: immunohistological demonstration of the involvement of 5-HT1B-receptors
J Longmore, Z Razzaque, D Shaw, et al.
Genomics
|
December 15, 1996
Genomic structure and chromosomal mapping of the mouse nov gene
M R Snaith, D Natarajan, L B Taylor, et al.
Journal of Cell Science
|
July 1, 1988
Insulin-like growth factors and the multiplication of Tera-2, a human teratoma-derived cell line
C Biddle, C H Li, P N Schofield, et al.
Journal of Medical Genetics
|
May 1, 1997
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome
D Catchpoole, W W Lam, D Valler, et al.
Veterinary Pathology
|
May 8, 2019
Hyaline Arteriolosclerosis in 30 Strains of Aged Inbred Mice
Timothy K Cooper, Kathleen A Silva, Victoria E Kennedy, et al.
Veterinary Pathology
|
March 4, 2016
Approaches to Investigating Complex Genetic Traits in a Large-Scale Inbred Mouse Aging Study
J P Sundberg, A Berndt, B A Sundberg, et al.
Page
of 24
Search research articles
Search
Showing results (171-180 of 231) with videos related to
Sort By:
Page
of 24
Human Molecular Genetics
|
September 1, 1997
Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome
J A Joyce, W K Lam, D J Catchpoole, et al.
Veterinary Pathology
|
September 7, 2010
Training pathologists in mouse pathology
J P Sundberg, J M Ward, H HogenEsch, 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.
Journal of Medical Genetics
|
January 11, 2000
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
J R Engel, A Smallwood, A Harper, et al.
British Journal of Clinical Pharmacology
|
December 23, 1998
Comparison of the vasoconstrictor effects of rizatriptan and sumatriptan in human isolated cranial arteries: immunohistological demonstration of the involvement of 5-HT1B-receptors
J Longmore, Z Razzaque, D Shaw, et al.
Genomics
|
December 15, 1996
Genomic structure and chromosomal mapping of the mouse nov gene
M R Snaith, D Natarajan, L B Taylor, et al.
Journal of Cell Science
|
July 1, 1988
Insulin-like growth factors and the multiplication of Tera-2, a human teratoma-derived cell line
C Biddle, C H Li, P N Schofield, et al.
Journal of Medical Genetics
|
May 1, 1997
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome
D Catchpoole, W W Lam, D Valler, et al.
Veterinary Pathology
|
May 8, 2019
Hyaline Arteriolosclerosis in 30 Strains of Aged Inbred Mice
Timothy K Cooper, Kathleen A Silva, Victoria E Kennedy, et al.
Veterinary Pathology
|
March 4, 2016
Approaches to Investigating Complex Genetic Traits in a Large-Scale Inbred Mouse Aging Study
J P Sundberg, A Berndt, B A Sundberg, et al.
Page
of 24