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Neuromolecular Medicine
|
May 2, 2013
Variant ataxia telangiectasia: clinical and molecular findings and evaluation of radiosensitive phenotypes in a patient and relatives
Kathleen Claes, Julie Depuydt, A Malcolm R Taylor, et al.
Xenotransplantation
|
October 3, 1999
IgY antiporcine endothelial cell antibodies effectively block human antiporcine xenoantibody binding
J Fryer, J Firca, J Leventhal, et al.
Acta Medica Scandinavica. Supplementum
|
January 1, 1988
Coronary events in the Hunter region of New South Wales, Australia: 1984-1986
A J Dobson, H M Alexander, K Al-Roomi, et al.
Peerj
|
November 29, 2023
Genomic analyses indicate resilience of a commercially and culturally important marine gastropod snail to climate change
Matt J Nimbs, Curtis Champion, Simon E Lobos, et al.
DNA Repair
|
September 24, 2004
The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4
Paula M Clements, Claire Breslin, Emma D Deeks, et al.
CBE Life Sciences Education
|
June 6, 2007
Genome Consortium for Active Teaching: meeting the goals of BIO2010
A Malcolm Campbell, Mary Lee S Ledbetter, Laura L M Hoopes, et al.
Bioorganic & Medicinal Chemistry
|
May 1, 1997
In vitro and ex vivo inhibition of hepatitis A virus 3C proteinase by a peptidyl monofluoromethyl ketone
T S Morris, S Frormann, S Shechosky, et al.
Nature Reviews. Disease Primers
|
September 21, 2019
Chromosome instability syndromes
A Malcolm R Taylor, Cynthia Rothblum-Oviatt, Nathan A Ellis, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 31, 2007
Mutation status of the residual ATM allele is an important determinant of the cellular response to chemotherapy and survival in patients with chronic lymphocytic leukemia containing an 11q deletion
Belinda Austen, Anna Skowronska, Claire Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 18, 2007
RIDDLE immunodeficiency syndrome is linked to defects in 53BP1-mediated DNA damage signaling
Grant S Stewart, Tatjana Stankovic, Philip J Byrd, et al.
Page
of 39
Search research articles
Search
Showing results (321-330 of 388) with videos related to
Sort By:
Page
of 39
Neuromolecular Medicine
|
May 2, 2013
Variant ataxia telangiectasia: clinical and molecular findings and evaluation of radiosensitive phenotypes in a patient and relatives
Kathleen Claes, Julie Depuydt, A Malcolm R Taylor, et al.
Xenotransplantation
|
October 3, 1999
IgY antiporcine endothelial cell antibodies effectively block human antiporcine xenoantibody binding
J Fryer, J Firca, J Leventhal, et al.
Acta Medica Scandinavica. Supplementum
|
January 1, 1988
Coronary events in the Hunter region of New South Wales, Australia: 1984-1986
A J Dobson, H M Alexander, K Al-Roomi, et al.
Peerj
|
November 29, 2023
Genomic analyses indicate resilience of a commercially and culturally important marine gastropod snail to climate change
Matt J Nimbs, Curtis Champion, Simon E Lobos, et al.
DNA Repair
|
September 24, 2004
The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4
Paula M Clements, Claire Breslin, Emma D Deeks, et al.
CBE Life Sciences Education
|
June 6, 2007
Genome Consortium for Active Teaching: meeting the goals of BIO2010
A Malcolm Campbell, Mary Lee S Ledbetter, Laura L M Hoopes, et al.
Bioorganic & Medicinal Chemistry
|
May 1, 1997
In vitro and ex vivo inhibition of hepatitis A virus 3C proteinase by a peptidyl monofluoromethyl ketone
T S Morris, S Frormann, S Shechosky, et al.
Nature Reviews. Disease Primers
|
September 21, 2019
Chromosome instability syndromes
A Malcolm R Taylor, Cynthia Rothblum-Oviatt, Nathan A Ellis, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
October 31, 2007
Mutation status of the residual ATM allele is an important determinant of the cellular response to chemotherapy and survival in patients with chronic lymphocytic leukemia containing an 11q deletion
Belinda Austen, Anna Skowronska, Claire Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 18, 2007
RIDDLE immunodeficiency syndrome is linked to defects in 53BP1-mediated DNA damage signaling
Grant S Stewart, Tatjana Stankovic, Philip J Byrd, et al.
Page
of 39