Kanno H - Search Results

1

Congenital anemia reveals distinct targeting mechanisms for master transcription factor GATA1.

Ludwig LS, Lareau CA, Bao EL, Liu N, Utsugisawa T, Tseng AM, Myers SA, Verboon JM, Ulirsch JC, Luo W, Muus C, Fiorini C, Olive ME, Vockley CM, Munschauer M, Hunter A, Ogura H, Yamamoto T, Inada H, Nakagawa S, Ohzono S, Subramanian V, Chiarle R, Glader B, Carr SA, Aryee MJ, Kundaje A, Orkin SH, Regev A, McCavit TL, Kanno H, Sankaran VG. Ludwig LS, et al. Among authors: kanno h. Blood. 2022 Apr 21;139(16):2534-2546. doi: 10.1182/blood.2021013753. Blood. 2022. PMID: 35030251 Free PMC article.

2

A new glucose-6-phosphate dehydrogenase variant (G6PD Tsukui) associated with congenital hemolytic anemia.

Ogura H, Morisaki T, Tani K, Kanno H, Tsutsumi H, Takahashi K, Miyamori T, Fujii H, Miwa S. Ogura H, et al. Among authors: kanno h. Hum Genet. 1988 Apr;78(4):369-71. doi: 10.1007/BF00291738. Hum Genet. 1988. PMID: 3360447

3

Delayed onset of hemolytic anemia in CBA-Pk-1slc/Pk-1slc mice with a point mutation of the gene encoding red blood cell type pyruvate kinase.

Tsujino K, Kanno H, Hashimoto K, Fujii H, Jippo T, Morii E, Lee YM, Asai H, Miwa S, Kitamura Y. Tsujino K, et al. Among authors: kanno h. Blood. 1998 Mar 15;91(6):2169-74. Blood. 1998. PMID: 9490705 Free article.

4

Transgenic rescue of hemolytic anemia due to red blood cell pyruvate kinase deficiency.

Kanno H, Utsugisawa T, Aizawa S, Koizumi T, Aisaki K, Hamada T, Ogura H, Fujii H. Kanno H, et al. Haematologica. 2007 Jun;92(6):731-7. doi: 10.3324/haematol.10945. Haematologica. 2007. PMID: 17550844 Free article.

5

Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression.

Viprakasit V, Ekwattanakit S, Riolueang S, Chalaow N, Fisher C, Lower K, Kanno H, Tachavanich K, Bejrachandra S, Saipin J, Juntharaniyom M, Sanpakit K, Tanphaichitr VS, Songdej D, Babbs C, Gibbons RJ, Philipsen S, Higgs DR. Viprakasit V, et al. Among authors: kanno h. Blood. 2014 Mar 6;123(10):1586-95. doi: 10.1182/blood-2013-09-526087. Epub 2014 Jan 17. Blood. 2014. PMID: 24443441 Free article.

6

[Glucose-6-phosphate dehydrogenase deficiency in Japan].

Kanno H, Ogura H. Kanno H, et al. Rinsho Ketsueki. 2015 Jul;56(7):771-7. doi: 10.11406/rinketsu.56.771. Rinsho Ketsueki. 2015. PMID: 26251139 Japanese.

7

ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia.

Arashiki N, Takakuwa Y, Mohandas N, Hale J, Yoshida K, Ogura H, Utsugisawa T, Ohga S, Miyano S, Ogawa S, Kojima S, Kanno H. Arashiki N, et al. Among authors: kanno h. Haematologica. 2016 May;101(5):559-65. doi: 10.3324/haematol.2016.142273. Epub 2016 Mar 4. Haematologica. 2016. PMID: 26944472 Free PMC article.

8

Erythrocyte glutathione is a novel biomarker of Diamond-Blackfan anemia.

Utsugisawa T, Uchiyama T, Toki T, Ogura H, Aoki T, Hamaguchi I, Ishiguro A, Ohara A, Kojima S, Ohga S, Ito E, Kanno H. Utsugisawa T, et al. Among authors: kanno h. Blood Cells Mol Dis. 2016 Jul;59:31-6. doi: 10.1016/j.bcmd.2016.03.007. Epub 2016 Apr 11. Blood Cells Mol Dis. 2016. PMID: 27282564

9

Splenectomy resolves hemolytic anemia caused by adenylate kinase deficiency.

Niizuma H, Kanno H, Sato A, Ogura H, Imaizumi M. Niizuma H, et al. Among authors: kanno h. Pediatr Int. 2017 Feb;59(2):228-230. doi: 10.1111/ped.13166. Pediatr Int. 2017. PMID: 28211224 No abstract available.

10

A novel PGK1 mutation associated with neurological dysfunction and the absence of episodes of hemolytic anemia or myoglobinuria.

Matsumaru S, Oguni H, Ogura H, Shimojima K, Nagata S, Kanno H, Yamamoto T. Matsumaru S, et al. Among authors: kanno h. Intractable Rare Dis Res. 2017 May;6(2):132-136. doi: 10.5582/irdr.2017.01020. Intractable Rare Dis Res. 2017. PMID: 28580215 Free PMC article.

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