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Science (New York, N.Y.)
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June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
E 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 Therapy
Adelya 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 cerebellum
Tao 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 study
Kwanza 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 trial
Neil 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 sizes
H 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 sequencing
H 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 divergence
H 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 gradient
Andrew 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 chromosomes
A M van den Ouweland, W H Deelen, C B Kunst, et al.
Page
of 48
Search research articles
Search
Showing results (371-380 of 471) with videos related to
Sort By:
Page
of 48
Science (New York, N.Y.)
|
June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
E 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 Therapy
Adelya 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 cerebellum
Tao 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 study
Kwanza 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 trial
Neil 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 sizes
H 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 sequencing
H 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 divergence
H 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 gradient
Andrew 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 chromosomes
A M van den Ouweland, W H Deelen, C B Kunst, et al.
Page
of 48