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Journal of Human Genetics (24)
Scientific Reports (8)
Oncogene (7)
Nature Genetics (6)
Modern Pathology (3)

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Showing 1–50 of 54 results

Advanced filters: Author: Johji Inazawa Clear advanced filters

Reexamination of chromosomal loci of human muscle actin genes by fluorescencein situ hybridization

Hisao Ueyama
Johji Inazawa
Takeshi Miwa
Research01 Mar 1995
Japanese journal of human genetics

Volume: 40, P: 145-148
Assignment of the human cytochrome P-450 nifedipine oxidase gene (CYP3A4) to chromosome 7 at band q22.1 by fluorescencein situ hybridization

Kiyoshi Inoue
Johji Inazawa
Tatsuo Abe
Research01 Jun 1992
Japanese journal of human genetics

Volume: 37, P: 133-138
Identification of an Efs isoform that lacks the SH3 domain and chromosomal mapping of human Efs

Masaho Ishino
Takeaki Ohba
Terukatsu Sasaki
Research02 Oct 1997
Oncogene

Volume: 15, P: 1741-1745
Fluorescencein situ hybridization analysis of chromosomal localization of three human cytochrome P450 2C genes (CYP2C8, 2C9, and 2C10) at 10q24.1

Kiyoshi Inoue
Johji Inazawa
Tatsuo Abe
Research01 Sept 1994
Japanese journal of human genetics

Volume: 39, P: 337-343
Therapeutic applications of local injection of hsa-miR-634 into canine spontaneous malignant melanoma tumors

Ryutaro Yoshikawa
Jun Inoue
Johji Inazawa
Research08 Aug 2023
Cancer Gene Therapy

Volume: 30, P: 1524-1529
A case of incomplete DiGeorge syndrome associated with partial monosomy 22q11.1 due to maternal 14;22 translocation

Sadayuki Nukina
Yasutaka Nishimura
Tatsuo Abe
Research01 Sept 1989
Japanese journal of human genetics

Volume: 34, P: 235-241
DNA analysis using long-term preserved fixed cytogenetic preparations

Hikari Nishigaki
Tsukasa Okuda
Tatsuo Abe
Research01 Dec 1988
Japanese journal of human genetics

Volume: 33, P: 417-421
ANA, a novel member of Tob/BTG1 family, is expressed in the ventricular zone of the developing central nervous system

Yutaka Yoshida
Satoru Matsuda
Tadashi Yamamoto
Research02 Jun 1998
Oncogene

Volume: 16, P: 2687-2693
Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta

Kiyonori Miura
Osamu Miyoshi
Tadayuki Ishimaru
Research01 Jan 1999
Journal of Human Genetics

Volume: 44, P: 1-9
Damaged epithelia regenerated by bone marrow–derived cells in the human gastrointestinal tract

Ryuichi Okamoto
Tomoharu Yajima
Mamoru Watanabe
Research26 Aug 2002
Nature Medicine

Volume: 8, P: 1011-1017
Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis

Shin Hayashi
Shozo Honda
Johji Inazawa
Research04 Apr 2007
Journal of Human Genetics

Volume: 52, P: 397-405
A novel metalloprotease/disintegrin–like gene at 17q21.3 is somatically rearranged in two primary breast cancers

Mitsuru Emi
Toyomasa Katagiri
Yusuke Nakamura
Research01 Oct 1993
Nature Genetics

Volume: 5, P: 151-157
Frequent association of alternative splicing of NER, a nuclear hormone receptor gene in cancer tissues

Hiroko Saito
Shyuichi Nakatsuru
Yusuke Nakamura
Research06 Feb 1997
Oncogene

Volume: 14, P: 617-621
Association of over-expressed TFDP1 with progression of hepatocellular carcinomas

Kohichiroh Yasui
Hiroyuki Okamoto
Johji Inazawa
Research15 Nov 2003
Journal of Human Genetics

Volume: 48, P: 609-613
GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell lines

Wei Yu
Jun Inoue
Johji Inazawa
Research29 Apr 2003
Journal of Human Genetics

Volume: 48, P: 331-335
Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population

Hidewaki Nakagawa and colleagues report a genome-wide association study for prostate cancer in a Japanese population. They replicate previously associated loci and identify five new susceptibility loci.

Ryo Takata
Shusuke Akamatsu
Hidewaki Nakagawa
Research01 Aug 2010
Nature Genetics

Volume: 42, P: 751-754
Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese

Hidewaki Nakagawa and colleagues identify three new genetic loci associated with prostate cancer in Japanese.

Shusuke Akamatsu
Ryo Takata
Hidewaki Nakagawa
Research26 Feb 2012
Nature Genetics

Volume: 44, P: 426-429
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations

Yataro Daigo and colleagues report a genome-wide association study for lung adenocarcinoma in Japanese and Korean populations, identifying a susceptibility locus at TP63.

Daiki Miki
Michiaki Kubo
Yataro Daigo
Research26 Sept 2010
Nature Genetics

Volume: 42, P: 893-896
Imaging flow cytometry-based multiplex FISH for three IGH translocations in multiple myeloma

Taku Tsukamoto
Masaki Kinoshita
Junya Kuroda
ResearchOpen Access08 Mar 2023
Journal of Human Genetics

Volume: 68, P: 507-514
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases

Genome-wide analysis in 212,453 Japanese individuals identifies loci associated with 42 diseases. Comparative analysis with European populations identifies East Asian–specific associations.

Kazuyoshi Ishigaki
Masato Akiyama
Yoichiro Kamatani
Research08 Jun 2020
Nature Genetics

Volume: 52, P: 669-679
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma

EGFR mutations in lung adenocarcinoma are more frequent in East Asians compared to other populations. Here, the authors carry out a genome-wide association study in EGFRmutant cancers and identify loci that are associated with risk of developing this molecular subtype of cancer.

Kouya Shiraishi
Yukinori Okada
Takashi Kohno
ResearchOpen Access09 Aug 2016
Nature Communications

Volume: 7, P: 1-7
12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population

More than 170 genetic loci have been linked to prostate cancer risk, primarily based on genome-wide association studies (GWAS) in European population. Here, the authors performed a GWAS on a Japanese cohort of prostate cancer patients, finding 12 new susceptibility loci, and identifying a polygenic risk for Japanese prostate cancer.

Ryo Takata
Atsushi Takahashi
Hidewaki Nakagawa
ResearchOpen Access27 Sept 2019
Nature Communications

Volume: 10, P: 1-10
Integrative cancer genomics in the era of precision cancer medicine

Johji Inazawa
Yoshio Miki
Yusuke Nakamura
Editorial16 Aug 2021
Journal of Human Genetics

Volume: 66, P: 843
Publisher Correction: miR-3140 suppresses tumor cell growth by targeting BRD4 via its coding sequence and downregulates the BRD4-NUT fusion oncoprotein

Erina Tonouchi
Yasuyuki Gen
Johji Inazawa
Amendments and CorrectionsOpen Access25 Apr 2018
Scientific Reports

Volume: 8, P: 1
Identical deletion at 14q13.3 including PAX9 and NKX2-1 in siblings from mosaicism of unaffected parent

Shin Hayashi
Mariko Yagi
Johji Inazawa
Research22 Jan 2015
Journal of Human Genetics

Volume: 60, P: 203-206
Identification and characterization of a 500-kb homozygously deleted region at 1p36.2-p36.3 in a neuroblastoma cell line

Miki Ohira
Hajime Kageyama
Akira Nakagawara
Research31 Aug 2000
Oncogene

Volume: 19, P: 4302-4307
Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion

Nana Okamoto
Shin Hayashi
Johji Inazawa
Research19 Jan 2012
Journal of Human Genetics

Volume: 57, P: 191-196
Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemia

Kazuhiro Fujita
Masashi Sanada
Issei Imoto
Research01 May 2009
Journal of Human Genetics

Volume: 54, P: 355-359
Actinin-4 gene amplification in ovarian cancer: a candidate oncogene associated with poor patient prognosis and tumor chemoresistance

Sohei Yamamoto
Hitoshi Tsuda
Osamu Matsubara
Research16 Jan 2009
Modern Pathology

Volume: 22, P: 499-507
Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation

Shozo Honda
Shigeko Satomura
Johji Inazawa
Research01 Dec 2011
Journal of Human Genetics

Volume: 57, P: 73-77
Translocation (1;22)(p36;q11.2) with concurrent del(22)(q11.2) resulted in homozygous deletion of SNF5/INI1 in a newly established cell line derived from extrarenal rhabdoid tumor

Akiko Misawa
Hajime Hosoi
Johji Inazawa
Research01 Oct 2004
Journal of Human Genetics

Volume: 49, P: 586-589
Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia

Takeshi Amino
Kinya Ishikawa
Hidehiro Mizusawa
Research05 Jul 2007
Journal of Human Genetics

Volume: 52, P: 643-649
Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation

Shozo Honda
Koji O Orii
Johji Inazawa
Research26 Mar 2010
Journal of Human Genetics

Volume: 55, P: 244-247
Cloning and expression of human B cell-specific transcription factor BACH2 mapped to chromosome 6q15

Shinya Sasaki
Etsuro Ito
Masaru Yokoyama
Research28 Jul 2000
Oncogene

Volume: 19, P: 3739-3749
Involvement of overexpressed wild-type BRAF in the growth of malignant melanoma cell lines

Hideaki Tanami
Issei Imoto
Johji Inazawa
Research04 Oct 2004
Oncogene

Volume: 23, P: 8796-8804
ADAM23, a possible tumor suppressor gene, is frequently silenced in gastric cancers by homozygous deletion or aberrant promoter hypermethylation

Hisashi Takada
Issei Imoto
Johji Inazawa
Research15 Aug 2005
Oncogene

Volume: 24, P: 8051-8060
Involvement of cyclin D3 in liver metastasis of colorectal cancer, revealed by genome-wide copy-number analysis

Hideaki Tanami
Hitoshi Tsuda
Johji Inazawa
Research27 Jun 2005
Laboratory Investigation

Volume: 85, P: 1118-1129
Mutations in EFHC1 cause juvenile myoclonic epilepsy

Toshimitsu Suzuki
Antonio V Delgado-Escueta
Kazuhiro Yamakawa
Research18 Jul 2004
Nature Genetics

Volume: 36, P: 842-849
miR-3140 suppresses tumor cell growth by targeting BRD4 via its coding sequence and downregulates the BRD4-NUT fusion oncoprotein

Erina Tonouchi
Yasuyuki Gen
Johji Inazawa
ResearchOpen Access14 Mar 2018
Scientific Reports

Volume: 8, P: 1-13
Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis

Shozo Honda
Shin Hayashi
Johji Inazawa
Research08 Jul 2010
Journal of Human Genetics

Volume: 55, P: 590-599
Isolation and characterisation of lymphatic endothelial cells from lung tissues affected by lymphangioleiomyomatosis

Koichi Nishino
Yasuhiro Yoshimatsu
Kuniaki Seyama
ResearchOpen Access16 Apr 2021
Scientific Reports

Volume: 11, P: 1-14
Copy number variation analysis in 83 children with early-onset developmental and epileptic encephalopathy after targeted resequencing of a 109-epilepsy gene panel

Kyoko Hirabayashi
Daniela Tiaki Uehara
Johji Inazawa
Research30 Aug 2019
Journal of Human Genetics

Volume: 64, P: 1097-1106
Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population

Siew-Kee Low
Yoon Ming Chin
Yoshio Miki
ResearchOpen Access22 Nov 2019
Scientific Reports

Volume: 9, P: 1-9
Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese

Kevin Y. Urayama
Masatoshi Takagi
Atsushi Manabe
ResearchOpen Access15 Jan 2018
Scientific Reports

Volume: 8, P: 1-9
miR-509-5p and miR-1243 increase the sensitivity to gemcitabine by inhibiting epithelial-mesenchymal transition in pancreatic cancer

Hidekazu Hiramoto
Tomoki Muramatsu
Johji Inazawa
ResearchOpen Access21 Jun 2017
Scientific Reports

Volume: 7, P: 1-12
Exosomal microRNA miR-1246 induces cell motility and invasion through the regulation of DENND2D in oral squamous cell carcinoma

Sujata Sakha
Tomoki Muramatsu
Johji Inazawa
ResearchOpen Access08 Dec 2016
Scientific Reports

Volume: 6, P: 1-11
Significant impact of miRNA–target gene networks on genetics of human complex traits

Yukinori Okada
Tomoki Muramatsu
Toshihiro Tanaka
ResearchOpen Access01 Mar 2016
Scientific Reports

Volume: 6, P: 1-9
SNP array screening of cryptic genomic imbalances in 450 Japanese subjects with intellectual disability and multiple congenital anomalies previously negative for large rearrangements

Daniela Tiaki Uehara
Shin Hayashi
Johji Inazawa
Research07 Jan 2016
Journal of Human Genetics

Volume: 61, P: 335-343
Actinin-4 expression in ovarian cancer: a novel prognostic indicator independent of clinical stage and histological type

Sohei Yamamoto
Hitoshi Tsuda
Osamu Matsubara
Research14 Sept 2007
Modern Pathology

Volume: 20, P: 1278-1285
Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies

Shin Hayashi
Issei Imoto
Johji Inazawa
Research28 Oct 2010
Journal of Human Genetics

Volume: 56, P: 110-124

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