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Scientific Reports
|
February 17, 2018
A hERG mutation E1039X produced a synergistic lesion on I<sub>Ks</sub> together with KCNQ1-R174C mutation in a LQTS family with three compound mutations
Jie Wu, Yuka Mizusawa, Seiko Ohno, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 2013
Millennial-scale isotope records from a wide-ranging predator show evidence of recent human impact to oceanic food webs
Anne E Wiley, Peggy H Ostrom, Andreanna J Welch, et al.
Neuro-Oncology
|
March 9, 2016
A new patient-derived orthotopic malignant meningioma model treated with oncolytic herpes simplex virus
Fares Nigim, Shin-Ichi Esaki, Michael Hood, et al.
Oncotarget
|
July 30, 2015
A high-throughput kinome screen reveals serum/glucocorticoid-regulated kinase 1 as a therapeutic target for NF2-deficient meningiomas
Roberta L Beauchamp, Marianne F James, Patrick A DeSouza, et al.
Journal of Neurointerventional Surgery
|
May 30, 2020
Delayed presentation of acute ischemic strokes during the COVID-19 crisis
Clemens M Schirmer, Andrew J Ringer, Adam S Arthur, et al.
Blood
|
March 11, 2015
The Bruton tyrosine kinase inhibitor ibrutinib with chemoimmunotherapy in patients with chronic lymphocytic leukemia
Jennifer R Brown, Jacqueline C Barrientos, Paul M Barr, et al.
Journal of Neurointerventional Surgery
|
August 14, 2014
Balloon-augmented Onyx embolization of cerebral arteriovenous malformations using a dual-lumen balloon: a multicenter experience
Alejandro M Spiotta, Robert F James, Stephen R Lowe, et al.
Neurobiology of Aging
|
September 1, 1989
Familial Alzheimer's disease: progress and problems
P H St George-Hyslop, R H Myers, J L Haines, et al.
Journal of the American College of Cardiology
|
December 27, 2014
Disturbance in Z-disk mechanosensitive proteins induced by a persistent mutant myopalladin causes familial restrictive cardiomyopathy
Anne-Cecile Huby, Uzmee Mendsaikhan, Ken Takagi, et al.
Archives of Disease in Childhood
|
May 1, 1996
Ionic control of beta cell function in nesidioblastosis. A possible therapeutic role for calcium channel blockade
K J Lindley, M J Dunne, C Kane, et al.
Page
of 102
Search research articles
Search
Showing results (911-920 of 1,011) with videos related to
Sort By:
Page
of 102
Scientific Reports
|
February 17, 2018
A hERG mutation E1039X produced a synergistic lesion on I<sub>Ks</sub> together with KCNQ1-R174C mutation in a LQTS family with three compound mutations
Jie Wu, Yuka Mizusawa, Seiko Ohno, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 15, 2013
Millennial-scale isotope records from a wide-ranging predator show evidence of recent human impact to oceanic food webs
Anne E Wiley, Peggy H Ostrom, Andreanna J Welch, et al.
Neuro-Oncology
|
March 9, 2016
A new patient-derived orthotopic malignant meningioma model treated with oncolytic herpes simplex virus
Fares Nigim, Shin-Ichi Esaki, Michael Hood, et al.
Oncotarget
|
July 30, 2015
A high-throughput kinome screen reveals serum/glucocorticoid-regulated kinase 1 as a therapeutic target for NF2-deficient meningiomas
Roberta L Beauchamp, Marianne F James, Patrick A DeSouza, et al.
Journal of Neurointerventional Surgery
|
May 30, 2020
Delayed presentation of acute ischemic strokes during the COVID-19 crisis
Clemens M Schirmer, Andrew J Ringer, Adam S Arthur, et al.
Blood
|
March 11, 2015
The Bruton tyrosine kinase inhibitor ibrutinib with chemoimmunotherapy in patients with chronic lymphocytic leukemia
Jennifer R Brown, Jacqueline C Barrientos, Paul M Barr, et al.
Journal of Neurointerventional Surgery
|
August 14, 2014
Balloon-augmented Onyx embolization of cerebral arteriovenous malformations using a dual-lumen balloon: a multicenter experience
Alejandro M Spiotta, Robert F James, Stephen R Lowe, et al.
Neurobiology of Aging
|
September 1, 1989
Familial Alzheimer's disease: progress and problems
P H St George-Hyslop, R H Myers, J L Haines, et al.
Journal of the American College of Cardiology
|
December 27, 2014
Disturbance in Z-disk mechanosensitive proteins induced by a persistent mutant myopalladin causes familial restrictive cardiomyopathy
Anne-Cecile Huby, Uzmee Mendsaikhan, Ken Takagi, et al.
Archives of Disease in Childhood
|
May 1, 1996
Ionic control of beta cell function in nesidioblastosis. A possible therapeutic role for calcium channel blockade
K J Lindley, M J Dunne, C Kane, et al.
Page
of 102