Chie Fujisawa
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Explore the profile of Chie Fujisawa including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
154
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Recent Articles
1.
Fujisawa C, Kodama H, Sato Y, Mimaki M, Yagi M, Awano H, et al.
Mol Genet Metab Rep
. 2022 Mar;
31:100849.
PMID: 35242581
Menkes disease (MD) is an X-linked recessive disorder caused by mutations in . Patients with MD exhibit severe neurological and connective tissue disorders due to copper deficiency and typically die...
2.
Fujisawa C, Hamanoue M, Kawano Y, Murata D, Akishima-Fukasawa Y, Okaneya T, et al.
J Invest Dermatol
. 2021 Dec;
142(7):1990-2002.e4.
PMID: 34929177
As a candidate microRNA antifibrotic effector in skin wounds, miR-146b-5p was upregulated by basic FGF, and PDGFRα was identified as a direct target of miR-146b-5p in fibroblasts. The treatment of...
3.
Fujisawa C, Kodama H, Hiroki T, Akasaka Y, Hamanoue M
Pediatr Int
. 2019 Feb;
61(4):345-350.
PMID: 30809870
Background: Menkes disease (MNK; MIN 309400) is an X-linked recessive lethal disorder of copper metabolism caused by mutations in ATP7A (MIM 300011), which encodes a transmembrane copper-transporting P-type ATPase. This...
4.
Nakamichi M, Akishima-Fukasawa Y, Fujisawa C, Mikami T, Onishi K, Akasaka Y
Am J Pathol
. 2016 Oct;
186(12):3203-3216.
PMID: 27773739
The role of fibrocytes in wound angiogenesis remains unclear. We therefore demonstrated the specific changes in fibrocyte accumulation for angiogesis in basic fibroblast growth factor (bFGF)-treated wounds. bFGF-treated wounds exhibited...
5.
Nomura S, Nozaki S, Hamazaki T, Takeda T, Ninomiya E, Kudo S, et al.
J Nucl Med
. 2014 Mar;
55(5):845-51.
PMID: 24627433
Unlabelled: Menkes disease (MD), an X-linked recessive disorder of copper metabolism caused by mutations in the copper-transporting ATP7A gene, results in growth failure and severe neurodegeneration in early childhood. Subcutaneous...
6.
Munakata M, Kodama H, Fujisawa C, Hiroki T, Kimura K, Watanabe M, et al.
Pediatr Res
. 2012 Jun;
72(3):270-6.
PMID: 22728746
Background: Menkes disease (MD) is a disorder of copper transport caused by ATP7A mutations. Although parenteral copper supplements are partly effective in treating MD, the copper level in the brain...
7.
Bhadhprasit W, Kodama H, Fujisawa C, Hiroki T, Ogawa E
J Trace Elem Med Biol
. 2012 Jun;
26(2-3):105-8.
PMID: 22664332
Menkes disease (MD) is a genetic neurodegenerative disorder characterized by copper deficiency due to a defect in ATP7A. Standard treatment involves parenteral copper-histidine administration. However, the treatment is ineffective if...
8.
Kodama H, Fujisawa C, Bhadhprasit W
Curr Drug Metab
. 2011 Aug;
13(3):237-50.
PMID: 21838703
Copper is an essential trace element required by all living organisms. Excess amounts of copper, however, results in cellular damage. Disruptions to normal copper homeostasis are hallmarks of three genetic...
9.
Kodama H, Fujisawa C, Shiga K
Nihon Rinsho
. 2011 Jul;
69 Suppl 1:752-7.
PMID: 21766693
No abstract available.
10.
Kodama H, Fujisawa C, Bhadhprasit W
Brain Dev
. 2010 Nov;
33(3):243-51.
PMID: 21112168
Genetic disorders of copper metabolism, including Menkes kinky hair disease (MD), occipital horn syndrome (OHS) and Wilson's disease (WD) are reviewed with a focus on the neurological aspects. MD and...