The movement disorder society criteria for the diagnosis of multiple system atrophy
…, M Stamelou, E Tolosa, S Tsuji… - Movement …, 2022 - Wiley Online Library
Background The second consensus criteria for the diagnosis of multiple system atrophy (MSA)
are widely recognized as the reference standard for clinical research, but lack sensitivity …
are widely recognized as the reference standard for clinical research, but lack sensitivity …
[HTML][HTML] Cyclooxygenase regulates angiogenesis induced by colon cancer cells
M Tsujii, S Kawano, S Tsuji, H Sawaoka, M Hori… - cell, 1998 - cell.com
… In spite of their efficacy as anticancer agents, the precise mechanism(s) for the protective …
verified by ethidium bromide staining of the gel and quantitation of the 18 S and 28 S bands. …
verified by ethidium bromide staining of the gel and quantitation of the 18 S and 28 S bands. …
Chronic endometritis and its effect on reproduction
…, S Tsuji, A Takashima, T Amano, S Tsuji… - Journal of Obstetrics …, 2019 - Wiley Online Library
Aim Chronic endometritis (CE) is a disease of continuous and subtle inflammation characterized
by the infiltration of plasma cells in the endometrial stromal area. Although the clinical …
by the infiltration of plasma cells in the endometrial stromal area. Although the clinical …
Primitive neural stem cells from the mammalian epiblast differentiate to definitive neural stem cells under the control of Notch signaling
…, S Kusunoki, I Kanazawa, S Tsuji… - Genes & …, 2004 - genesdev.cshlp.org
… However, these same survival factors appear not to increase the frequency of isolating
primitive neural stem cells from the epiblast (S. Hitoshi, unpubl.), suggesting that only a few …
primitive neural stem cells from the epiblast (S. Hitoshi, unpubl.), suggesting that only a few …
[HTML][HTML] Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
…, N Tayebi, T Toda, AR Troiano, S Tsuji… - … England Journal of …, 2009 - Mass Medical Soc
Background Recent studies indicate an increased frequency of mutations in the gene
encoding glucocerebrosidase (GBA), a deficiency of which causes Gaucher's disease, among …
encoding glucocerebrosidase (GBA), a deficiency of which causes Gaucher's disease, among …
Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)
…, M Saito, A Tomoda, T Miike, H Naito, F Ikuta, S Tsuji - Nature …, 1994 - nature.com
Hereditary dentatorubral–pallidoluysian atrophy (DRPLA) is an autosomal dominant
neurologic disorder characterized by variable combinations of myoclonus, epilepsy, cerebellar …
neurologic disorder characterized by variable combinations of myoclonus, epilepsy, cerebellar …
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
…, O Evgrafov, PD Jonghe, Y Takahashi, S Tsuji… - Nature …, 2004 - nature.com
We report missense mutations in the mitochondrial fusion protein mitofusin 2 (MFN2) in
seven large pedigrees affected with Charcot-Marie-Tooth neuropathy type 2A (CMT2A). …
seven large pedigrees affected with Charcot-Marie-Tooth neuropathy type 2A (CMT2A). …
[HTML][HTML] Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Background We aimed to accurately estimate the frequency of a hexanucleotide repeat
expansion in C9orf72 that has been associated with a large proportion of cases of amyotrophic …
expansion in C9orf72 that has been associated with a large proportion of cases of amyotrophic …
Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
…, K Iwabuchi, I Eguchi, H Tanaka, H Takahashi, S Tsuji - Nature …, 1996 - nature.com
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant, neurodegenerative
disorder that affects the cerebellum and other areas of the central nervous system. We have …
disorder that affects the cerebellum and other areas of the central nervous system. We have …
[HTML][HTML] Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bβ
…, S Terada, T Nakata, Y Takei, M Saito, S Tsuji… - Cell, 2001 - cell.com
The kinesin superfamily motor protein KIF1B has been shown to transport mitochondria.
Here, we describe an isoform of KIF1B, KIF1Bβ, that is distinct from KIF1B in its cargo binding …
Here, we describe an isoform of KIF1B, KIF1Bβ, that is distinct from KIF1B in its cargo binding …