N Ohkoshi
Overview
Explore the profile of N Ohkoshi including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
97
Citations
595
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Imagawa S, Matsumoto K, Horie M, Ohkoshi N, Nagasawa T, Doi T, et al.
Int J Sports Med
. 2007 May;
28(11):928-33.
PMID: 17497587
Erythropoietin gene expression is stimulated by hypoxia-inducible factor 1 and inhibited by GATA. Thus, drugs that attenuate the action of GATA and/or potentiate the action of HIF-1 may increase Epo...
2.
Zeng Q, Isobe K, Fu L, Ohkoshi N, Ohmori H, Takekoshi K, et al.
Life Sci
. 2006 Oct;
80(5):454-9.
PMID: 17070556
Adiponectin reportedly reduces insulin-resistance. Exercise has also been shown to lessen insulin-resistance, though it is not known whether exercise increases levels of adiponectin and/or its receptors or whether its effects...
3.
Ohto T, Iwasaki N, Fujiwara J, Ohkoshi N, Kimura S, Kawade K, et al.
Neuropediatrics
. 2004 Nov;
35(5):274-8.
PMID: 15534759
We report on a 10-year-old girl with anhidrosis and insensibility to pain, but no severe mental retardation or self-mutilation, diagnosed as hereditary sensory and autonomic neuropathy type IV (HSAN IV)....
4.
Ohkoshi N, Ishii A, Shoji S
J Clin Neurosci
. 2004 Jun;
11(5):566-7.
PMID: 15177416
This case report describes a 46-year-old man whose first symptom was an attack of acute flank pain, followed by the gradual onset neurological symptoms. We demonstrated a small nidus and...
5.
Tomimitsu H, Shimizu J, Ishikawa K, Ohkoshi N, Kanazawa I, Mizusawa H
Neurology
. 2004 May;
62(9):1607-10.
PMID: 15136692
Study of the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene (GNE) revealed that almost all cases of distal myopathy with rimmed vacuoles were caused by GNE mutations. Seven new mutations were identified, including...
6.
Ishii A, Hayashi A, Ohkoshi N, Matsuno S, Shoji S
J Neurol Neurosurg Psychiatry
. 2004 Mar;
75(4):661-2.
PMID: 15026525
No abstract available.
7.
Watanabe M, Harada S, Nakamura T, Ohkoshi N, Yoshizawa K, Hayashi A, et al.
Neuropsychobiology
. 2003 Dec;
48(4):190-3.
PMID: 14673217
Catechol-O-methyltransferase (COMT) is an enzyme that inactivates catecholamines, including levodopa. An amino acid change (Val-108-Met) in the COMT protein has been found to result in a change from high to...
8.
Watanabe M, Yamamoto N, Ohkoshi N, Nagata H, Kohno Y, Hayashi A, et al.
Neurology
. 2002 Sep;
59(5):767-9.
PMID: 12221176
A patient with hereditary neuropathy presented with asymmetric distal weakness. On nerve biopsy, there was demyelination and onion-bulb formation, and molecular analysis revealed that the patient was heterozygous for an...
9.
Tomimitsu H, Ishikawa K, Shimizu J, Ohkoshi N, Kanazawa I, Mizusawa H
Neurology
. 2002 Aug;
59(3):451-4.
PMID: 12177386
The authors present three novel missense mutations in the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene, the causative gene for hereditary inclusion body myopathy, in Japanese patients with distal myopathy with rimmed...
10.