About: Noriyoshi Fukushima

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Japanese pathologist

Attributes	Values
rdf:type	Item
description	wetenschapper (nl) дослідник (uk) Japanese pathologist (en) patólogo japonés (es) 日本の病理医 (ja) عالم أمراض ياباني (ar) patólogu xaponés (ast)
rdfs:label	Noriyoshi Fukushima (en) Noriyoshi Fukushima (nl) Noriyoshi Fukushima (tr) Noriyoshi Fukushima (ast) 福嶋敬宜 (ja)
skos:prefLabel	Noriyoshi Fukushima (en) Noriyoshi Fukushima (nl) Noriyoshi Fukushima (tr) Noriyoshi Fukushima (ast) 福嶋敬宜 (ja)
name	Noriyoshi Fukushima (en) Noriyoshi Fukushima (nl) Noriyoshi Fukushima (tr) Noriyoshi Fukushima (ast) 福嶋敬宜 (ja)
given name	wds:Q91795800-F86EDDE3-5D40-4BF2-8ACE-6A012DF83768
given name	Noriyoshi
instance of	wds:Q91795800-1DB7B328-CFC9-4CE6-BD57-4D1A96F805EE
instance of	Homo sapiens
Researchmap ID	wds:Q91795800-91523F57-4D26-41D1-84C3-489792E4BBD5
Researchmap ID	D-Pathology
skos:altLabel	Fukushima Noriyoshi (en) ふくしまのりよし (ja) フクシマノリヨシ (ja)
occupation	wds:Q91795800-59C93FC8-64E5-4B8C-88E9-6CE30024B170
employer	wds:Q91795800-0685b4c9-40ad-7aba-bb46-cc905c2d1bad wds:Q91795800-fc70f542-4674-db97-d2dc-6aa142f165c0 wds:Q91795800-fca87c9e-47c2-63e5-00a6-3416a795920b
CiNii Research ID	wds:Q91795800-5C0E880B-D885-41AC-B7E5-33FC4513F716
name in native language	wds:Q91795800-cbf30869-4d3c-d616-1324-c6bc4202da3c
sex or gender	wds:Q91795800-8b049443-42fb-12ce-38bc-2b69738d9b9c
VIAF ID	wds:Q91795800-1b8841cb-4728-25d5-96f0-0677d0522a25
country of citizenship	wds:Q91795800-d034f421-4266-dc9d-fced-27689c954b60
NACSIS-CAT author ID	wds:q91795800-299fa835-4092-eb40-f774-c62ca7f5af4d
NDL Authority ID	wds:q91795800-89c4a374-496b-eac5-d895-f7ee8cf93865
family name	wds:Q91795800-2096c76f-467b-d51a-7831-1c25007febfd
J-GLOBAL ID	wds:Q91795800-09D7AD49-6293-4B03-B916-FC8EEE53038B
WorldCat Identities ID (superseded)	wds:q91795800-39f9dc27-4174-8eff-f947-f404b5c2e995
CiNii Research ID	https://cir.nii.ac.jp/crid/1420282801197172992.rdf
VIAF ID	http://viaf.org/viaf/252746304
NACSIS-CAT author ID	https://ci.nii.ac.jp/author/DA14618861#entity
NDL Authority ID	http://id.ndl.go.jp/auth/ndlna/00976184
occupation	pathologist
employer	University of Tokyo Jichi Medical University Johns Hopkins Medicine
CiNii Research ID	1420282801197172992
name in native language	福嶋敬宜 (ja-hani)
sex or gender	male
VIAF ID	252746304
country of citizenship	Japan
NACSIS-CAT author ID	DA14618861
NDL Authority ID	00976184
family name	Fukushima
J-GLOBAL ID	201401077459790889
WorldCat Identities ID (superseded)	viaf-252746304
ORCID iD	wds:Q91795800-AC0D2A2E-62B7-43D3-A6C6-9015A19271EE
ORCID iD	https://orcid.org/0000-0002-4522-9007
ORCID iD	0000-0002-4522-9007
e-Rad researcher number	wds:Q91795800-1A3B5AD5-903B-4EB9-8833-8BC2113DB3C7
e-Rad researcher number	40384937
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q91795800
is author of	Gene expression profiles in pancreatic intraepithelial neoplasia reflect the effects of Hedgehog signaling on pancreatic ductal epithelial cells. Real-time identification of liver cancers by using indocyanine green fluorescent imaging Genome-wide allelotypes of familial pancreatic adenocarcinomas and familial and sporadic intraductal papillary mucinous neoplasms Epigenetic inactivation of TFPI-2 as a common mechanism associated with growth and invasion of pancreatic ductal adenocarcinoma. Different subtypes of intraductal papillary mucinous neoplasm in the pancreas have distinct pathways to pancreatic cancer progression Aberrant methylation of Reprimo correlates with genetic instability and predicts poor prognosis in pancreatic ductal adenocarcinoma SPARC/osteonectin is a frequent target for aberrant methylation in pancreatic adenocarcinoma and a mediator of tumor-stromal interactions The Human MitoChip: a high-throughput sequencing microarray for mitochondrial mutation detection. Polymorphisms of SPINK1 N34S and CFTR in patients with sporadic and familial pancreatic cancer. CpG island methylation profile of pancreatic intraepithelial neoplasia Frequent hypomethylation of multiple genes overexpressed in pancreatic ductal adenocarcinoma. Aberrant methylation of the 5' CpG island of TSLC1 is common in pancreatic ductal adenocarcinoma and is first manifest in high-grade PanlNs Characterization of gene expression in mucinous cystic neoplasms of the pancreas using oligonucleotide microarrays Aberrant methylation of preproenkephalin and p16 genes in pancreatic intraepithelial neoplasia and pancreatic ductal adenocarcinoma Serum macrophage inhibitory cytokine 1 as a marker of pancreatic and other periampullary cancers Differentiating pancreatic lesions by microarray and QPCR analysis of pancreatic juice RNAs. Intraductal papillary mucinous neoplasms of the pancreas: an updated experience Diagnostic utility of biopsy specimens for autoimmune pancreatitis. Epigenetic down-regulation of CDKN1C/p57KIP2 in pancreatic ductal neoplasms identified by gene expression profiling Ribonucleotide reductase subunit M2 mRNA expression in pretreatment biopsies obtained from unresectable pancreatic carcinomas The chemokine receptor CXCR4 is regulated by DNA methylation in pancreatic cancer. An illustrated consensus on the classification of pancreatic intraepithelial neoplasia and intraductal papillary mucinous neoplasms Gene expression profiling identifies genes associated with invasive intraductal papillary mucinous neoplasms of the pancreas Precursors to invasive pancreatic cancer Classification of types of intraductal papillary-mucinous neoplasm of the pancreas: a consensus study Aberrant methylation of CpG islands in intraductal papillary mucinous neoplasms of the pancreas. Identification of maspin and S100P as novel hypomethylation targets in pancreatic cancer using global gene expression profiling Methylation of cyclin D2 is observed frequently in pancreatic cancer but is also an age-related phenomenon in gastrointestinal tissues Diagnosing pancreatic cancer using methylation specific PCR analysis of pancreatic juice. LigAmp for sensitive detection of single-nucleotide differences.

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