Sakoe K[au] - Search Results

Year	Number of Results
1992	1
1993	1
1994	1
1995	3
1997	2
1998	3
1999	2
2000	2
2001	3
2002	3
2004	1
2005	1
2006	2
2007	2
2008	2
2009	1
2010	3
2011	1
2012	3
2013	1
2020	1
2021	1
2022	0

1

A newly identified NES sequence present in spastin regulates its subcellular localization and microtubule severing activity.

Sakoe K, Shioda N, Matsuura T. Sakoe K, et al. Biochim Biophys Acta Mol Cell Res. 2021 Jan;1868(1):118862. doi: 10.1016/j.bbamcr.2020.118862. Epub 2020 Sep 24. Biochim Biophys Acta Mol Cell Res. 2021. PMID: 32979422 Free article.

2

Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature.

Namekawa M, Takiyama Y, Honda J, Shimazaki H, Sakoe K, Nakano I. Namekawa M, et al. Among authors: sakoe k. BMC Neurol. 2010 Apr 1;10:21. doi: 10.1186/1471-2377-10-21. BMC Neurol. 2010. PMID: 20359319 Free PMC article. Review.

3

NF-κB mediates aberrant activation of HIF-1 in malignant lymphoma.

Qiao Q, Nozaki Y, Sakoe K, Komatsu N, Kirito K. Qiao Q, et al. Among authors: sakoe k. Exp Hematol. 2010 Dec;38(12):1199-208. doi: 10.1016/j.exphem.2010.08.007. Epub 2010 Sep 24. Exp Hematol. 2010. PMID: 20813154

4

Middle cerebellar peduncles and Pontine T2 hypointensities in ARSACS.

Shimazaki H, Takiyama Y, Honda J, Sakoe K, Namekawa M, Tsugawa J, Tsuboi Y, Suzuki C, Baba M, Nakano I. Shimazaki H, et al. Among authors: sakoe k. J Neuroimaging. 2013 Jan;23(1):82-5. doi: 10.1111/j.1552-6569.2011.00647.x. Epub 2012 Jan 23. J Neuroimaging. 2013. PMID: 22268491

5

A phenotype without spasticity in sacsin-related ataxia.

Shimazaki H, Takiyama Y, Sakoe K, Ando Y, Nakano I. Shimazaki H, et al. Among authors: sakoe k. Neurology. 2005 Jun 28;64(12):2129-31. doi: 10.1212/01.WNL.0000166031.91514.B3. Neurology. 2005. PMID: 15985586

6

Sacsin-related ataxia (ARSACS): expanding the genotype upstream from the gigantic exon.

Ouyang Y, Takiyama Y, Sakoe K, Shimazaki H, Ogawa T, Nagano S, Yamamoto Y, Nakano I. Ouyang Y, et al. Among authors: sakoe k. Neurology. 2006 Apr 11;66(7):1103-4. doi: 10.1212/01.wnl.0000204300.94261.ea. Neurology. 2006. PMID: 16606928

7

A novel RUNX1 mutation in familial platelet disorder with propensity to develop myeloid malignancies.

Kirito K, Sakoe K, Shinoda D, Takiyama Y, Kaushansky K, Komatsu N. Kirito K, et al. Among authors: sakoe k. Haematologica. 2008 Jan;93(1):155-6. doi: 10.3324/haematol.12050. Haematologica. 2008. PMID: 18166807 Free article.

8

16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.

Ouyang Y, Sakoe K, Shimazaki H, Namekawa M, Ogawa T, Ando Y, Kawakami T, Kaneko J, Hasegawa Y, Yoshizawa K, Amino T, Ishikawa K, Mizusawa H, Nakano I, Takiyama Y. Ouyang Y, et al. Among authors: sakoe k. J Neurol Sci. 2006 Sep 25;247(2):180-6. doi: 10.1016/j.jns.2006.04.009. Epub 2006 Jun 15. J Neurol Sci. 2006. PMID: 16780885

9

Inhibition of hypoxia-inducible factor-1 function enhances the sensitivity of multiple myeloma cells to melphalan.

Hu Y, Kirito K, Yoshida K, Mitsumori T, Nakajima K, Nozaki Y, Hamanaka S, Nagashima T, Kunitama M, Sakoe K, Komatsu N. Hu Y, et al. Among authors: sakoe k. Mol Cancer Ther. 2009 Aug;8(8):2329-38. doi: 10.1158/1535-7163.MCT-09-0150. Epub 2009 Aug 11. Mol Cancer Ther. 2009. PMID: 19671732

10

FOXO3A as a key molecule for all-trans retinoic acid-induced granulocytic differentiation and apoptosis in acute promyelocytic leukemia.

Sakoe Y, Sakoe K, Kirito K, Ozawa K, Komatsu N. Sakoe Y, et al. Among authors: sakoe k. Blood. 2010 May 6;115(18):3787-95. doi: 10.1182/blood-2009-05-222976. Epub 2010 Mar 9. Blood. 2010. PMID: 20215638 Free article.

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