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Nature
|
January 24, 1970
Increases in serum lactate dehydrogenase in experimental allergic encephalomyelitis
A E Kaplan, L V Brown, J Salk
Cancer Research
|
June 11, 2009
Cancer genome sequencing--an interim analysis
Edward J Fox, Jesse J Salk, Lawrence A Loeb
Annual Review of Pathology
|
September 12, 2009
Mutational heterogeneity in human cancers: origin and consequences
Jesse J Salk, Edward J Fox, Lawrence A Loeb
Nature Reviews. Genetics
|
March 27, 2018
Enhancing the accuracy of next-generation sequencing for detecting rare and subclonal mutations
Jesse J Salk, Michael W Schmitt, Lawrence A Loeb
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 1, 1985
Pseudotumour cerebri and the Turner syndrome
V P Sybert, T D Bird, D J Salk
Aging Cell
|
June 5, 2014
Response to: 'when man got his mtDNA deletions?'
Sean D Taylor, Jesse J Salk, Jason H Bielas
American Journal of Medical Genetics
|
January 1, 1981
Brief clinical report: the del(4) (q31) syndrome- a recognizable disorder with atypical Robin malformation sequence
J M Davis, S K Clarren, D J Salk
Genome Medicine
|
March 19, 2016
Exploring the implications of distinct mutational signatures and mutation rates in aging and cancer
Edward J Fox, Jesse J Salk, Lawrence A Loeb
Nature Reviews. Clinical Oncology
|
October 21, 2015
The influence of subclonal resistance mutations on targeted cancer therapy
Michael W Schmitt, Lawrence A Loeb, Jesse J Salk
Proceedings of the National Academy of Sciences of the United States of America
|
April 8, 2014
Risks of double-counting in deep sequencing
Michael W Schmitt, Edward J Fox, Jesse J Salk
Page
of 12
Search research articles
Search
Showing results (31-40 of 113) with videos related to
Sort By:
Page
of 12
Nature
|
January 24, 1970
Increases in serum lactate dehydrogenase in experimental allergic encephalomyelitis
A E Kaplan, L V Brown, J Salk
Cancer Research
|
June 11, 2009
Cancer genome sequencing--an interim analysis
Edward J Fox, Jesse J Salk, Lawrence A Loeb
Annual Review of Pathology
|
September 12, 2009
Mutational heterogeneity in human cancers: origin and consequences
Jesse J Salk, Edward J Fox, Lawrence A Loeb
Nature Reviews. Genetics
|
March 27, 2018
Enhancing the accuracy of next-generation sequencing for detecting rare and subclonal mutations
Jesse J Salk, Michael W Schmitt, Lawrence A Loeb
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 1, 1985
Pseudotumour cerebri and the Turner syndrome
V P Sybert, T D Bird, D J Salk
Aging Cell
|
June 5, 2014
Response to: 'when man got his mtDNA deletions?'
Sean D Taylor, Jesse J Salk, Jason H Bielas
American Journal of Medical Genetics
|
January 1, 1981
Brief clinical report: the del(4) (q31) syndrome- a recognizable disorder with atypical Robin malformation sequence
J M Davis, S K Clarren, D J Salk
Genome Medicine
|
March 19, 2016
Exploring the implications of distinct mutational signatures and mutation rates in aging and cancer
Edward J Fox, Jesse J Salk, Lawrence A Loeb
Nature Reviews. Clinical Oncology
|
October 21, 2015
The influence of subclonal resistance mutations on targeted cancer therapy
Michael W Schmitt, Lawrence A Loeb, Jesse J Salk
Proceedings of the National Academy of Sciences of the United States of America
|
April 8, 2014
Risks of double-counting in deep sequencing
Michael W Schmitt, Edward J Fox, Jesse J Salk
Page
of 12