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Cell Reports
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June 18, 2025
The evolutionarily conserved PRP4K-CHMP4B/vps32 splicing circuit regulates autophagy
Sabateeshan Mathavarajah, Sandhya Chipurupalli, Elias B Habib, et al.
Annals of Neurology
|
December 1, 1996
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients
M Ikeda, V Sharma, S M Sumi, et al.
Nature Genetics
|
September 10, 1998
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
J Liu, M Aoki, I Illa, et al.
Neurology
|
July 27, 2001
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy
M Aoki, J Liu, I Richard, et al.
European Journal of Neurology
|
April 14, 2019
Longitudinal changes in <sup>18</sup> F-THK5351 positron emission tomography in corticobasal syndrome
M Ezura, A Kikuchi, A Ishiki, et al.
Physical Review Letters
|
August 29, 2015
Improved Measurement of the π→eν Branching Ratio
A Aguilar-Arevalo, M Aoki, M Blecher, et al.
Science (New York, N.Y.)
|
August 25, 1995
The effect of magmatic activity on hydrothermal venting along the superfast-spreading East pacific rise
T Urabe, E T Baker, J Ishibashi, et al.
Neurology
|
June 11, 2003
Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype
T Takahashi, M Aoki, M Tateyama, et al.
Physical Review Letters
|
November 5, 2004
New limit on the T-violating transverse muon polarization in K+-->pi0mu+nu decays
M Abe, M Aliev, V Anisimovsky, et al.
Physical Review Letters
|
September 26, 2012
Search for violation of Lorentz invariance in top quark pair production and decay
V M Abazov, B Abbott, B S Acharya, et al.
Page
of 114
Search research articles
Search
Showing results (731-740 of 1,138) with videos related to
Sort By:
Page
of 114
Cell Reports
|
June 18, 2025
The evolutionarily conserved PRP4K-CHMP4B/vps32 splicing circuit regulates autophagy
Sabateeshan Mathavarajah, Sandhya Chipurupalli, Elias B Habib, et al.
Annals of Neurology
|
December 1, 1996
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients
M Ikeda, V Sharma, S M Sumi, et al.
Nature Genetics
|
September 10, 1998
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
J Liu, M Aoki, I Illa, et al.
Neurology
|
July 27, 2001
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy
M Aoki, J Liu, I Richard, et al.
European Journal of Neurology
|
April 14, 2019
Longitudinal changes in <sup>18</sup> F-THK5351 positron emission tomography in corticobasal syndrome
M Ezura, A Kikuchi, A Ishiki, et al.
Physical Review Letters
|
August 29, 2015
Improved Measurement of the π→eν Branching Ratio
A Aguilar-Arevalo, M Aoki, M Blecher, et al.
Science (New York, N.Y.)
|
August 25, 1995
The effect of magmatic activity on hydrothermal venting along the superfast-spreading East pacific rise
T Urabe, E T Baker, J Ishibashi, et al.
Neurology
|
June 11, 2003
Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype
T Takahashi, M Aoki, M Tateyama, et al.
Physical Review Letters
|
November 5, 2004
New limit on the T-violating transverse muon polarization in K+-->pi0mu+nu decays
M Abe, M Aliev, V Anisimovsky, et al.
Physical Review Letters
|
September 26, 2012
Search for violation of Lorentz invariance in top quark pair production and decay
V M Abazov, B Abbott, B S Acharya, et al.
Page
of 114