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Nature
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January 1, 1999
Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy
B C Schroeder, C Kubisch, V Stein, et al.
Obstetrics and Gynecology
|
May 1, 1995
Epidural analgesia and uterine function
E R Newton, B C Schroeder, K G Knape, et al.
The Journal of Biological Chemistry
|
May 19, 2000
KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents
B C Schroeder, M Hechenberger, F Weinreich, et al.
Epilepsia
|
August 29, 2000
Pathophysiology of KCNQ channels: neonatal epilepsy and progressive deafness
T J Jentsch, B C Schroeder, C Kubisch, et al.
Human Molecular Genetics
|
September 25, 1997
Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias
B Wollnik, B C Schroeder, C Kubisch, et al.
Nature
|
January 26, 2000
A constitutively open potassium channel formed by KCNQ1 and KCNE3
B C Schroeder, S Waldegger, S Fehr, et al.
Science (New York, N.Y.)
|
February 7, 1998
A potassium channel mutation in neonatal human epilepsy
C Biervert, B C Schroeder, C Kubisch, et al.
Cell
|
February 20, 1999
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness
C Kubisch, B C Schroeder, T Friedrich, et al.
The Journal of Chemical Physics
|
October 2, 2024
Core and valence photoelectron spectroscopy of a series of substituted disulfides
H G McGhee, R Totani, O Plekan, et al.
Journal of the American Chemical Society
|
February 27, 2019
Spectroscopic Investigation of the Effect of Microstructure and Energetic Offset on the Nature of Interfacial Charge Transfer States in Polymer: Fullerene Blends
S D Dimitrov, M Azzouzi, J Wu, et al.
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Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Nature
|
January 1, 1999
Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy
B C Schroeder, C Kubisch, V Stein, et al.
Obstetrics and Gynecology
|
May 1, 1995
Epidural analgesia and uterine function
E R Newton, B C Schroeder, K G Knape, et al.
The Journal of Biological Chemistry
|
May 19, 2000
KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents
B C Schroeder, M Hechenberger, F Weinreich, et al.
Epilepsia
|
August 29, 2000
Pathophysiology of KCNQ channels: neonatal epilepsy and progressive deafness
T J Jentsch, B C Schroeder, C Kubisch, et al.
Human Molecular Genetics
|
September 25, 1997
Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias
B Wollnik, B C Schroeder, C Kubisch, et al.
Nature
|
January 26, 2000
A constitutively open potassium channel formed by KCNQ1 and KCNE3
B C Schroeder, S Waldegger, S Fehr, et al.
Science (New York, N.Y.)
|
February 7, 1998
A potassium channel mutation in neonatal human epilepsy
C Biervert, B C Schroeder, C Kubisch, et al.
Cell
|
February 20, 1999
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness
C Kubisch, B C Schroeder, T Friedrich, et al.
The Journal of Chemical Physics
|
October 2, 2024
Core and valence photoelectron spectroscopy of a series of substituted disulfides
H G McGhee, R Totani, O Plekan, et al.
Journal of the American Chemical Society
|
February 27, 2019
Spectroscopic Investigation of the Effect of Microstructure and Energetic Offset on the Nature of Interfacial Charge Transfer States in Polymer: Fullerene Blends
S D Dimitrov, M Azzouzi, J Wu, et al.
Page
of 1