Please enable Javascript

Labmeeting uses lots of Javascript - basically you can't use the site without it. So please enable Javascript in your browser. If your browser does not support Javascript, we recommend Firefox.

Papers authored by Kunishima S

Collect these papers and discover other ones on Labmeeting. Learn more.

Mutations in MYH9 exons 1, 16, 26, and 30 are infrequently found in Japanese patients with nonsyndromic deafness.

+ cite this

+ View Abstract

Kunishima S, Matsunaga T, Ito Y, and Saito H

Genetic testing and molecular biomarkers 13(5):705-7, 2009 Oct - Who cited this? | PubMed ID: 19645626 | Fulltext

A novel homozygous 8-base pair deletion mutation in the glycoprotein Ibalpha gene in a patient with Bernard-Soulier syndrome.

+ cite this

+ View Abstract

Imai C, Kunishima S, Takachi T, Iwabuchi H, Nemoto T, Imamura M, and Uchiyama M

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 20(6):470-4, 2009 Sep - Who cited this? | PubMed ID: 19448529 | Fulltext

Identification of three in-frame deletion mutations in MYH9 disorders suggesting an important hot spot for small rearrangements in MYH9 exon 24.

+ cite this

+ View Abstract

Miyazaki K, Kunishima S, Fujii W, and Higashihara M

European journal of haematology 83(3):230-4, 2009 Sep - Who cited this? | PubMed ID: 19459928 | Fulltext

A rare case of MYH9 disorders presenting with macrothrombocytopenia and deafness caused by MYH9-R702C mutation.

+ cite this

Kodama R, Taketani T, Kunishima S, Mishima S, Yoshikawa Y, Kanai R, Suyama T, Yoshino I, Kunishi H, Shibata H, Nagai A, Yamaguchi S, and Masuda J

Thrombosis research 124(4):508-11, 2009 Sep - Who cited this? | PubMed ID: 19250658 | Fulltext

Identification of the first in cis mutations in MYH9 disorder.

+ cite this

+ View Abstract

Miyajima Y and Kunishima S

European journal of haematology 82(4):288-91, 2009 Apr - Who cited this? | PubMed ID: 19191864 | Fulltext

[Autosomal dominant macrothrombocytopenia with leukocyte inclusion bodies and MYH9 disorders].

+ cite this

+ View Abstract

Kunishima S

Rinsho byori. The Japanese journal of clinical pathology 57(4):365-70, 2009 Apr - Who cited this? | PubMed ID: 19489439 | Fulltext

Germinal mosaicism in MYH9 disorders: a family with two affected siblings of normal parents.

+ cite this

Kunishima S, Takaki K, Ito Y, and Saito H

British journal of haematology 145(2):260-2, 2009 Apr - Who cited this? | PubMed ID: 19208103 | Fulltext

May-hegglin anomaly: morphologic and clinical manifestations.

+ cite this

Saito H and Kunishima S

Clinical advances in hematology & oncology : H&O 7(2):111-3, 2009 Feb - Who cited this? | PubMed ID: 19367252 | Fulltext

Mutation of the beta1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly.

+ cite this

+ View Abstract

Kunishima S, Kobayashi R, Itoh TJ, Hamaguchi M, and Saito H

Blood 113(2):458-61, 2009 Jan 8 - Who cited this? | PubMed ID: 18849486 | Fulltext

[May-Hegglin anomaly: past and present--novel diagnostic test and new concept of the disease].

+ cite this

+ View Abstract

Kunishima S

Rinsho byori. The Japanese journal of clinical pathology 57(1):54-9, 2009 Jan - Who cited this? | PubMed ID: 19227191 | Fulltext

Usefulness of immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A for diagnosing in two sisters with May-Hegglin anomaly.

+ cite this

+ View Abstract

Kimura N, Matsumoto M, Matsumoto K, Asai N, and Kunishima S

[Rinsho ketsueki] The Japanese journal of clinical hematology 49(12):1614-8, 2008 Dec - Who cited this? | PubMed ID: 19110523 | Fulltext

Mutational analysis of SOS1 gene in acute myeloid leukemia.

+ cite this

Tanizaki R, Katsumi A, Kiyoi H, Kunishima S, Iwasaki T, Ishikawa Y, Kobayashi M, Abe A, Matsushita T, Watanabe T, Kojima T, Kaibuchi K, Kojima S, and Naoe T

International journal of hematology 88(4):460-2, 2008 Nov - Who cited this? | PubMed ID: 18972187 | Fulltext

Accumulation of MYH9 mRNA at leukocyte inclusion bodies in MYH9 disorders.

+ cite this

Kunishima S, Hirano K, Hamaguchi M, and Saito H

European journal of haematology, 2008 Jun 30 - Who cited this? | PubMed ID: 18616507 | Fulltext

Identification and characterization of the first large deletion of the MYH9 gene associated with MYH9 disorders.

+ cite this

+ View Abstract

Kunishima S, Matsushita T, Hamaguchi M, and Saito H

European journal of haematology 80(6):540, 2008 Jun - Who cited this? | PubMed ID: 18284620 | Fulltext

Characterization of a patient with atypical amegakaryocytic thrombocytopenia.

+ cite this

+ View Abstract

Kanaji S, Kanaji T, Migita M, Kunishima S, Kunicki TJ, Okamura T, and Izuhara K

European journal of haematology 80(4):361, 2008 Apr - Who cited this? | PubMed ID: 18194481 | Fulltext

Historical hematology: May-Hegglin anomaly.

+ cite this

+ View Abstract

Saito H and Kunishima S

American journal of hematology 83(4):304, 2008 Apr - Who cited this? | PubMed ID: 17975807 | Fulltext

Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders.

+ cite this

+ View Abstract

Kunishima S, Hamaguchi M, and Saito H

Blood 111(6):3015, 2008 Mar 15 - Who cited this? | PubMed ID: 18192507 | Fulltext

Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations.

+ cite this

+ View Abstract

Kunishima S, Yoshinari M, Nishio H, Ida K, Miura T, Matsushita T, Hamaguchi M, and Saito H

European journal of haematology 78(3):220, 2007 Mar - Who cited this? | PubMed ID: 17241369 | Fulltext

First Turkish case of Bernard-Soulier syndrome associated with GPIX N45S.

+ cite this

+ View Abstract

Dağistan N and Kunishima S

Acta haematologica 118(3):146, 2007 - Who cited this? | PubMed ID: 17804902 | Fulltext

Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutations.

+ cite this

+ View Abstract

Kunishima S, Sako M, Yamazaki T, Hamaguchi M, and Saito H

European journal of haematology 77(6):501, 2006 Dec - Who cited this? | PubMed ID: 16978236 | Fulltext

Identification of a novel MYH9 mutation in a patient with May-Hegglin anomaly.

+ cite this

Otsubo K, Kanegane H, Nomura K, Ogawa J, Miyawaki T, and Kunishima S

Pediatric blood & cancer 47(7):968, 2006 Dec - Who cited this? | PubMed ID: 16642488 | Fulltext

A case of myelofibrosis with myeloid metaplasia with JAK2(V617F) mutation who developed fibrous tumours in multiple organs.

+ cite this

Tabuchi T, Ohashi H, Fukami S, Susaki N, Kunishima S, Yokozawa T, Nagai H, Moritani S, Ichihara S, Saito H, and Hamaguchi M

European journal of haematology 77(3):264-6, 2006 Sep - Who cited this? | PubMed ID: 16923114 | Fulltext

In vitro characterization of missense mutations associated with quantitative protein S deficiency.

+ cite this

+ View Abstract

Okada H, Yamazaki T, Takagi A, Murate T, Yamamoto K, Takamatsu J, Matsushita T, Naoe T, Kunishima S, Hamaguchi M, Saito H, and Kojima T

Journal of thrombosis and haemostasis : JTH 4(9):2003-9, 2006 Sep - Who cited this? | PubMed ID: 16961607 | Fulltext

Bernard-Soulier syndrome due to GPIX W127X mutation in Japan is frequently misdiagnosed as idiopathic thrombocytopenic purpura.

+ cite this

Kunishima S, Yamada T, Hamaguchi M, and Saito H

International journal of hematology 83(4):366, 2006 May - Who cited this? | PubMed ID: 16757441 | Fulltext

Novel heterozygous missense mutation in the second leucine rich repeat of GPIbalpha affects GPIb/IX/V expression and results in macrothrombocytopenia in a patient initially misdiagnosed with idiopathic thrombocytopenic purpura.

+ cite this

+ View Abstract

Kunishima S, Imai T, Hamaguchi M, and Saito H

European journal of haematology 76(4):348, 2006 Apr - Who cited this? | PubMed ID: 16519708 | Fulltext

Congenital macrothrombocytopenias.

+ cite this

+ View Abstract

Kunishima S and Saito H

Blood reviews 20(2):111-21, 2006 Mar - Who cited this? | PubMed ID: 16169642 | Fulltext

Further characterization of anti-platelet monoclonal antibody HPL5 as anti-glycoprotein V antibody.

+ cite this

Kunishima S, Motoyama M, Takagi A, Hamaguchi M, Kojima T, and Saito H

Acta haematologica 115(1-2):128-30, 2006 - Who cited this? | PubMed ID: 16424664 | Fulltext

First description of somatic mosaicism in MYH9 disorders.

+ cite this

+ View Abstract

Kunishima S, Matsushita T, Yoshihara T, Nakase Y, Yokoi K, Hamaguchi M, and Saito H

British journal of haematology 128(3):360-5, 2005 Feb - Who cited this? | PubMed ID: 15667538 | Fulltext

Detection of unique neutrophil non-muscle myosin heavy chain-A localization by immunofluorescence analysis in MYH9 disorder presented with macrothrombocytopenia without leukocyte inclusions and deafness.

+ cite this

+ View Abstract

Kunishima S, Matsushita T, Shiratsuchi M, Ikuta T, Nishimura J, Hamaguchi M, Naoe T, and Saito H

European journal of haematology 74(1):1, 2005 Jan - Who cited this? | PubMed ID: 15613099 | Fulltext

Giant platelet syndrome.

+ cite this

Saito H, Matsushita T, Yamamoto K, Kojima T, and Kunishima S

Hematology (Amsterdam, Netherlands) 10 Suppl 1:41-6, 2005 - Who cited this? | PubMed ID: 16188632 | Fulltext

Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO mice.

+ cite this

+ View Abstract

Matsushita T, Hayashi H, Kunishima S, Hayashi M, Ikejiri M, Takeshita K, Yuzawa Y, Adachi T, Hirashima K, Sone M, Yamamoto K, Takagi A, Katsumi A, Kawai K, Nezu T, Takahashi M,

(show remaining authors)

Biochemical and biophysical research communications 325(4):1163-71, 2004 Dec 24 - Who cited this? | PubMed ID: 15555549 | Fulltext

A unique immunofluorescence method promotes accurate diagnosis in MYH9 disorders: a case report.

+ cite this

+ View Abstract

Yoshinari M, Kunishima S, Miyabayashi S, Saito H, and Tsuchiya S

Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 26(9):579-83, 2004 Sep - Who cited this? | PubMed ID: 15342975 | Fulltext

Relationships between oxygen and glucose metabolism in human liver tumours: positron emission tomography using (15)O and (18)F-deoxyglucose.

+ cite this

+ View Abstract

Fukuda K, Taniguchi H, Koh T, Kunishima S, and Yamagishi H

Nuclear medicine communications 25(6):577-83, 2004 Jun - Who cited this? | PubMed ID: 15167517 | Fulltext

Differential diagnosis of gallbladder cancer using positron emission tomography with fluorine-18-labeled fluoro-deoxyglucose (FDG-PET).

+ cite this

+ View Abstract

Koh T, Taniguchi H, Yamaguchi A, Kunishima S, and Yamagishi H

Journal of surgical oncology 84(2):74-81, 2003 Oct - Who cited this? | PubMed ID: 14502780 | Fulltext

[May-Hegglin anomaly--from genome research to clinical laboratory].

+ cite this

+ View Abstract

Kunishima S

Rinsho byori. The Japanese journal of clinical pathology 51(9):898-904, 2003 Sep - Who cited this? | PubMed ID: 14560660 | Fulltext

The reproducibility of independently measuring human regional hepatic arterial, portal and total hepatic blood flow using [15O]water and positron emission tomography.

+ cite this

+ View Abstract

Taniguchi H, Kunishima S, and Koh T

Nuclear medicine communications 24(5):497-501, 2003 May - Who cited this? | PubMed ID: 12717065 | Fulltext

Expression of low-frequency Ala108Pro substitution in the platelet glycoprotein Ibbeta gene.

+ cite this

+ View Abstract

Kunishima S, Gassner C, Inoue C, Kamiya T, and Ozawa K

European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 30(2):159-61, 2003 Apr - Who cited this? | PubMed ID: 12648286 | Fulltext

GATA-1 transcription factor is mutated in CMK megakaryoblastic cell line.

+ cite this

Kunishima S, Kojima T, Inoue C, Kamiya T, and Saito H

British journal of haematology 120(3):542-3, 2003 Feb - Who cited this? | PubMed ID: 12580977 | Fulltext

Changes in hepatic parenchymal blood flow with colorectal metastases: increase in arterial and decrease in portal blood flow.

+ cite this

+ View Abstract

Kunishima S, Taniguchi H, Yamaguchi A, Koh T, and Yamagishi H

Hepato-gastroenterology 50(53):1457-62, 2003 - Who cited this? | PubMed ID: 14571763 | Fulltext

Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations.

+ cite this

+ View Abstract

Kunishima S, Matsushita T, Kojima T, Sako M, Kimura F, Jo EK, Inoue C, Kamiya T, and Saito H

Laboratory investigation; a journal of technical methods and pathology 83(1):115-22, 2003 Jan - Who cited this? | PubMed ID: 12533692 | Fulltext

Novel nonsense mutation in the platelet glycoprotein Ibbeta gene associated with Bernard-Soulier syndrome.

+ cite this

+ View Abstract

Kunishima S, Matsushita T, Ito T, Kamiya T, and Saito H

American journal of hematology 71(4):279, 2002 Dec - Who cited this? | PubMed ID: 12447957 | Fulltext

Genetic abnormalities of Bernard-Soulier syndrome.

+ cite this

+ View Abstract

Kunishima S, Kamiya T, and Saito H

International journal of hematology 76(4):319, 2002 Nov - Who cited this? | PubMed ID: 12463594 | Fulltext

Quantitative measurement of regional blood flow in hepatic focal nodular hyperplasia. Findings on positron emission tomography.

+ cite this

+ View Abstract

Kunishima S, Koh T, Fukuda K, and Taniguchi H

Molecular imaging and biology : MIB : the official publication of the Academy of Molecular Imaging 4(3):253-6, 2002 May - Who cited this? | PubMed ID: 14537130 | Fulltext

Are both PIVKA-II and alpha-fetoprotein necessary in follow-up management after hepatic resection for hepatocellular carcinoma?.

+ cite this

+ View Abstract

Koh T, Taniguchi H, Katoh H, Kunishima S, Yamaguchi A, and Yamagishi H

Hepato-gastroenterology 49(48):1615-8, 2002 - Who cited this? | PubMed ID: 12397748 | Fulltext

Novel heterozygous missense mutation in the platelet glycoprotein Ib beta gene associated with isolated giant platelet disorder.

+ cite this

+ View Abstract

Kunishima S, Naoe T, Kamiya T, and Saito H

American journal of hematology 68(4):249-55, 2001 Dec - Who cited this? | PubMed ID: 11754414 | Fulltext

A missense mutation (Tyr88 to Cys) in the platelet membrane glycoprotein Ibbeta gene affects GPIb/IX complex expression--Bernard-Soulier syndrome in the homozygous form and giant platelets in the heterozygous form.

+ cite this

+ View Abstract

Kurokawa Y, Ishida F, Kamijo T, Kunishima S, Kenny D, Kitano K, and Koike K

Thrombosis and haemostasis 86(5):1249-56, 2001 Nov - Who cited this? | PubMed ID: 11816714 | Fulltext

F-18 fluorodeoxyglucose positron emission tomography in mesenterial Castleman's lymphoma.

+ cite this

Kunishima S, Taniguchi H, Koh T, Yamaguchi A, and Yamagishi H

Clinical nuclear medicine 26(9):789-90, 2001 Sep - Who cited this? | PubMed ID: 11507303 | Fulltext

Presence of Propionibacterium acnes in blood components.

+ cite this

+ View Abstract

Kunishima S, Inoue C, Kamiya T, and Ozawa K

Transfusion 41(9):1126-9, 2001 Sep - Who cited this? | PubMed ID: 11552069 | Fulltext

Reproducibility of repeated human regional splenic blood flow measurements using [15O] water and positron emission tomography.

+ cite this

+ View Abstract

Taniguch H, Kunishima S, Koh T, Oguro A, and Yamagishi H

Nuclear medicine communications 22(7):755-7, 2001 Jul - Who cited this? | PubMed ID: 11453047 | Fulltext

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).

+ cite this

+ View Abstract

Kunishima S, Kojima T, Matsushita T, Tanaka T, Tsurusawa M, Furukawa Y, Nakamura Y, Okamura T, Amemiya N, Nakayama T, Kamiya T, and Saito H

Blood 97(4):1147-9, 2001 Feb 15 - Who cited this? | PubMed ID: 11159552 | Fulltext

Search Google Scholar for Kunishima S

Join Labmeeting

Organize and search your PDF collection
Collect papers
Search millions of papers
Keep up to date with paper alerts
Read your papers from anywhere
Recommend papers to colleagues
Manage your lab

Labmeeting is a web service for researchers. Sign up with your academic email address.

Individuals or corporations not affiliated with an academic institution can request a trial subscription.

Got a question?
The Labmeeting Network
has the answer.
Ask scientists at top universities like Harvard, Stanford, and MIT for their expert opinion!