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T Warren

Showing results (371-380 of 471) with videos related to

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Science (New York, N.Y.)|June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)nE J Kremer, M Pritchard, M Lynch, et al.
Counselling Psychology Quarterly|January 23, 2023
The beginning of the end: A comparison of treatment completers and early dropouts in trainee-provided time-limited Cognitive Behavioral TherapyAdelya A Urmanche, Lauren M Lipner, Sarah Bloch-Elkouby, et al.
Human Molecular Genetics|October 9, 2012
Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellumTao Wang, Qian Pan, Li Lin, et al.
CNS Oncology|October 28, 2020
Time to treatment initiation and outcomes in high-grade glioma patients in rehabilitation: a retrospective cohort studyKwanza T Warren, Linxi Liu, Yang Liu, et al.
Regional Anesthesia and Pain Medicine|August 21, 2021
Comparison of continuous intravenous lidocaine versus transversus abdominis plane block for kidney transplant surgery: a randomized, non-inferiority trialNeil A Hanson, Joseph Strunk, Genna Saunders, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2017
Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizesH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
PEMapper and PECaller provide a simplified approach to whole-genome sequencingH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 1998
A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergenceH H Chou, H Takematsu, S Diaz, et al.
Aging Cell|July 29, 2016
Prelamin A impairs 53BP1 nuclear entry by mislocalizing NUP153 and disrupting the Ran gradientAndrew M Cobb, Delphine Larrieu, Derek T Warren, et al.
Human Molecular Genetics|October 1, 1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomesA M van den Ouweland, W H Deelen, C B Kunst, et al.
Pageof 48

Showing results (371-380 of 471) with videos related to

Sort By:
Pageof 48
Science (New York, N.Y.)|June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)nE J Kremer, M Pritchard, M Lynch, et al.
Counselling Psychology Quarterly|January 23, 2023
The beginning of the end: A comparison of treatment completers and early dropouts in trainee-provided time-limited Cognitive Behavioral TherapyAdelya A Urmanche, Lauren M Lipner, Sarah Bloch-Elkouby, et al.
Human Molecular Genetics|October 9, 2012
Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellumTao Wang, Qian Pan, Li Lin, et al.
CNS Oncology|October 28, 2020
Time to treatment initiation and outcomes in high-grade glioma patients in rehabilitation: a retrospective cohort studyKwanza T Warren, Linxi Liu, Yang Liu, et al.
Regional Anesthesia and Pain Medicine|August 21, 2021
Comparison of continuous intravenous lidocaine versus transversus abdominis plane block for kidney transplant surgery: a randomized, non-inferiority trialNeil A Hanson, Joseph Strunk, Genna Saunders, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2017
Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizesH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
PEMapper and PECaller provide a simplified approach to whole-genome sequencingH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 1998
A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergenceH H Chou, H Takematsu, S Diaz, et al.
Aging Cell|July 29, 2016
Prelamin A impairs 53BP1 nuclear entry by mislocalizing NUP153 and disrupting the Ran gradientAndrew M Cobb, Delphine Larrieu, Derek T Warren, et al.
Human Molecular Genetics|October 1, 1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomesA M van den Ouweland, W H Deelen, C B Kunst, et al.
Pageof 48