Kunishima S - Search Results

1

GPIbα is required for platelet-mediated hepatic thrombopoietin generation.

Xu M, Li J, Neves MAD, Zhu G, Carrim N, Yu R, Gupta S, Marshall J, Rotstein O, Peng J, Hou M, Kunishima S, Ware J, Branch DR, Lazarus AH, Ruggeri ZM, Freedman J, Ni H. Xu M, et al. Among authors: kunishima s. Blood. 2018 Aug 9;132(6):622-634. doi: 10.1182/blood-2017-12-820779. Epub 2018 May 24. Blood. 2018. PMID: 29794068 Free article.

2

Bernard-Soulier syndrome Kagoshima: Ser 444-->stop mutation of glycoprotein (GP) Ib alpha resulting in circulating truncated GPIb alpha and surface expression of GPIb beta and GPIX.

Kunishima S, Miura H, Fukutani H, Yoshida H, Osumi K, Kobayashi S, Ohno R, Naoe T. Kunishima S, et al. Blood. 1994 Nov 15;84(10):3356-62. Blood. 1994. PMID: 7949089 Free article.

3

Missense mutations of the glycoprotein (GP) Ib beta gene impairing the GPIb alpha/beta disulfide linkage in a family with giant platelet disorder.

Kunishima S, Lopez JA, Kobayashi S, Imai N, Kamiya T, Saito H, Naoe T. Kunishima S, et al. Blood. 1997 Apr 1;89(7):2404-12. Blood. 1997. PMID: 9116284 Free article.

4

Diagnostic biomarker for ACTN1 macrothrombocytopenia.

Kunishima S, Kitamura K, Yasutomi M, Kobayashi R. Kunishima S, et al. Blood. 2015 Nov 26;126(22):2525-6. doi: 10.1182/blood-2015-08-666180. Epub 2015 Oct 15. Blood. 2015. PMID: 26472750 Free article. No abstract available.

5

Linkage between the mechanisms of thrombocytopenia and thrombopoiesis.

Eto K, Kunishima S. Eto K, et al. Among authors: kunishima s. Blood. 2016 Mar 10;127(10):1234-41. doi: 10.1182/blood-2015-07-607903. Epub 2016 Jan 19. Blood. 2016. PMID: 26787737 Free PMC article. Review.

6

Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia.

Sivapalaratnam S, Westbury SK, Stephens JC, Greene D, Downes K, Kelly AM, Lentaigne C, Astle WJ, Huizinga EG, Nurden P, Papadia S, Peerlinck K, Penkett CJ, Perry DJ, Roughley C, Simeoni I, Stirrups K, Hart DP, Tait RC, Mumford AD; NIHR BioResource; Laffan MA, Freson K, Ouwehand WH, Kunishima S, Turro E. Sivapalaratnam S, et al. Among authors: kunishima s. Blood. 2017 Jan 26;129(4):520-524. doi: 10.1182/blood-2016-08-732248. Epub 2016 Nov 14. Blood. 2017. PMID: 28064200 Free PMC article.

7

Increased but highly dispersed levels of plasma glycocalicin in patients with disseminated intravascular coagulation.

Kunishima S, Kobayashi S, Naoe T. Kunishima S, et al. Eur J Haematol. 1996 Mar;56(3):173-7. doi: 10.1111/j.1600-0609.1996.tb01338.x. Eur J Haematol. 1996. PMID: 8598238

8

Serum thrombopoietin and plasma glycocalicin concentrations as useful diagnostic markers in thrombocytopenic disorders.

Kunishima S, Tahara T, Kato T, Kobayashi S, Saito H, Naoe T. Kunishima S, et al. Eur J Haematol. 1996 Jul;57(1):68-71. doi: 10.1111/j.1600-0609.1996.tb00492.x. Eur J Haematol. 1996. PMID: 8698134

9

De novo mutation of the platelet glycoprotein Ib alpha gene in a patient with pseudo-von Willebrand disease.

Kunishima S, Heaton DC, Naoe T, Hickton C, Mizuno S, Saito H, Kamiya T. Kunishima S, et al. Blood Coagul Fibrinolysis. 1997 Jul;8(5):311-5. doi: 10.1097/00001721-199707000-00009. Blood Coagul Fibrinolysis. 1997. PMID: 9282797

10

Homozygous Pro74-->Arg mutation in the platelet glycoprotein Ibbeta gene associated with Bernard-Soulier syndrome.

Kunishima S, Tomiyama Y, Honda S, Fukunishi M, Hara J, Inoue C, Kamiya T, Saito H. Kunishima S, et al. Thromb Haemost. 2000 Jul;84(1):112-7. Thromb Haemost. 2000. PMID: 10928480

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