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Eye (London, England)
|
August 15, 2009
ARMS2/HTRA1 and CFH polymorphisms are not associated with choroidal neovascularization in highly myopic eyes of the elderly Japanese population
H Nakanishi, N Gotoh, R Yamada, et al.
Archives of Virology
|
January 1, 1996
Molecular characterization of feline immunodeficiency virus genome obtained directly from organs of a naturally infected cat with marked neurological symptoms and encephalitis
Y Nishimura, S Nakamura, N Goto, et al.
Science (New York, N.Y.)
|
July 11, 1997
Murine model of Niemann-Pick C disease: mutation in a cholesterol homeostasis gene
S K Loftus, J A Morris, E D Carstea, et al.
Journal of Medicinal Chemistry
|
May 23, 2000
Novel antiarthritic agents with 1,2-isothiazolidine-1,1-dioxide (gamma-sultam) skeleton: cytokine suppressive dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase
M Inagaki, T Tsuri, H Jyoyama, et al.
Nanoscale
|
January 9, 2018
Extensive first-principles molecular dynamics study on Li encapsulation into C<sub>60</sub> and its experimental confirmation
K Ohno, A Manjanath, Y Kawazoe, et al.
Human Molecular Genetics
|
May 1, 1997
Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene: identification and functional characterization of six new mutations
K Ohno, P A Quiram, M Milone, et al.
Research in Veterinary Science
|
May 21, 2021
Construction and validation of a scoring system to predict resistance to chemotherapeutic drugs using gene expression profiles in canine lymphoma
A Tani, Y Saegusa, K Ogawa, et al.
Human Genetics
|
September 10, 1999
NPC1 gene mutations in Japanese patients with Niemann-Pick disease type C
T Yamamoto, E Nanba, H Ninomiya, et al.
Neurology
|
September 25, 1999
Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene
L Middleton, K Ohno, K Christodoulou, et al.
Chemical Communications (Cambridge, England)
|
May 24, 2012
Tuning glycosidase inhibition through aglycone interactions: pharmacological chaperones for Fabry disease and GM1 gangliosidosis
M Aguilar-Moncayo, T Takai, K Higaki, et al.
Page
of 74
Search research articles
Search
Showing results (721-730 of 737) with videos related to
Sort By:
Page
of 74
Eye (London, England)
|
August 15, 2009
ARMS2/HTRA1 and CFH polymorphisms are not associated with choroidal neovascularization in highly myopic eyes of the elderly Japanese population
H Nakanishi, N Gotoh, R Yamada, et al.
Archives of Virology
|
January 1, 1996
Molecular characterization of feline immunodeficiency virus genome obtained directly from organs of a naturally infected cat with marked neurological symptoms and encephalitis
Y Nishimura, S Nakamura, N Goto, et al.
Science (New York, N.Y.)
|
July 11, 1997
Murine model of Niemann-Pick C disease: mutation in a cholesterol homeostasis gene
S K Loftus, J A Morris, E D Carstea, et al.
Journal of Medicinal Chemistry
|
May 23, 2000
Novel antiarthritic agents with 1,2-isothiazolidine-1,1-dioxide (gamma-sultam) skeleton: cytokine suppressive dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase
M Inagaki, T Tsuri, H Jyoyama, et al.
Nanoscale
|
January 9, 2018
Extensive first-principles molecular dynamics study on Li encapsulation into C<sub>60</sub> and its experimental confirmation
K Ohno, A Manjanath, Y Kawazoe, et al.
Human Molecular Genetics
|
May 1, 1997
Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene: identification and functional characterization of six new mutations
K Ohno, P A Quiram, M Milone, et al.
Research in Veterinary Science
|
May 21, 2021
Construction and validation of a scoring system to predict resistance to chemotherapeutic drugs using gene expression profiles in canine lymphoma
A Tani, Y Saegusa, K Ogawa, et al.
Human Genetics
|
September 10, 1999
NPC1 gene mutations in Japanese patients with Niemann-Pick disease type C
T Yamamoto, E Nanba, H Ninomiya, et al.
Neurology
|
September 25, 1999
Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene
L Middleton, K Ohno, K Christodoulou, et al.
Chemical Communications (Cambridge, England)
|
May 24, 2012
Tuning glycosidase inhibition through aglycone interactions: pharmacological chaperones for Fabry disease and GM1 gangliosidosis
M Aguilar-Moncayo, T Takai, K Higaki, et al.
Page
of 74