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K Ohno

Showing results (701-710 of 737) with videos related to

Pageof 74
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Elife|September 13, 2017
Cell type boundaries organize plant developmentMonica Pia Caggiano, Xiulian Yu, Neha Bhatia, et al.
Neuron|July 1, 1996
Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunitK Ohno, H L Wang, M Milone, et al.
Neurology|February 28, 2002
Three novel COLQ mutations and variation of phenotypic expressivity due to G240XY A Shapira, M E Sadeh, M P Bergtraum, et al.
Nature Neuroscience|April 9, 1999
Acetylcholine receptor M3 domain: stereochemical and volume contributions to channel gatingH L Wang, M Milone, K Ohno, et al.
The Journal of General Physiology|August 30, 2000
Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndromeH L Wang, K Ohno, M Milone, et al.
Neuron|April 16, 1998
Mode switching kinetics produced by a naturally occurring mutation in the cytoplasmic loop of the human acetylcholine receptor epsilon subunitM Milone, H L Wang, K Ohno, et al.
Clinical Genetics|June 2, 2016
Characterization of SPATA5-related encephalopathy in early childhoodH Kurata, H Terashima, M Nakashima, et al.
The Journal of Toxicological Sciences|June 13, 2001
[Toxicity study of cefmatilen hydrochloride hydrate (S-1090) (5)--Six-month repeated oral dose toxicity study and supplement study in rats]H Sameshima, M Omori, Y Nishimura, et al.
Nihon Jibiinkoka Gakkai Kaiho|February 3, 2000
[Analysis of outcome of free jejunal-autograft for head and neck reconstruction--postoperative complications and functional results of swallowing in 49 cases]K Yamada, S Fukuda, K Yagi, et al.
Human Genetics|November 10, 2001
Association between nasal allergy and a coding variant of the Fc epsilon RI beta gene Glu237Gly in a Japanese populationH Nagata, H Mutoh, K Kumahara, et al.
Pageof 74

Showing results (701-710 of 737) with videos related to

Sort By:
Pageof 74
Elife|September 13, 2017
Cell type boundaries organize plant developmentMonica Pia Caggiano, Xiulian Yu, Neha Bhatia, et al.
Neuron|July 1, 1996
Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunitK Ohno, H L Wang, M Milone, et al.
Neurology|February 28, 2002
Three novel COLQ mutations and variation of phenotypic expressivity due to G240XY A Shapira, M E Sadeh, M P Bergtraum, et al.
Nature Neuroscience|April 9, 1999
Acetylcholine receptor M3 domain: stereochemical and volume contributions to channel gatingH L Wang, M Milone, K Ohno, et al.
The Journal of General Physiology|August 30, 2000
Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndromeH L Wang, K Ohno, M Milone, et al.
Neuron|April 16, 1998
Mode switching kinetics produced by a naturally occurring mutation in the cytoplasmic loop of the human acetylcholine receptor epsilon subunitM Milone, H L Wang, K Ohno, et al.
Clinical Genetics|June 2, 2016
Characterization of SPATA5-related encephalopathy in early childhoodH Kurata, H Terashima, M Nakashima, et al.
The Journal of Toxicological Sciences|June 13, 2001
[Toxicity study of cefmatilen hydrochloride hydrate (S-1090) (5)--Six-month repeated oral dose toxicity study and supplement study in rats]H Sameshima, M Omori, Y Nishimura, et al.
Nihon Jibiinkoka Gakkai Kaiho|February 3, 2000
[Analysis of outcome of free jejunal-autograft for head and neck reconstruction--postoperative complications and functional results of swallowing in 49 cases]K Yamada, S Fukuda, K Yagi, et al.
Human Genetics|November 10, 2001
Association between nasal allergy and a coding variant of the Fc epsilon RI beta gene Glu237Gly in a Japanese populationH Nagata, H Mutoh, K Kumahara, et al.
Pageof 74