top of page
​研究業績

査読付き論文 (15 報)

15.  Y. Ochi, A. Kon, T. Sakata, M. M. Nakagawa, N. Nakazawa, M. Kakuta, K. Kataoka, H. Koseki, M. Nakayama, D. Morishita, T. Tsuruyama, R. Saiki, A. Yoda, R. Okuda, T. Yoshizato, Y. Shiozawa, Y. Nannya, S. Kotani, Y. Kogure, N. Kakiuchi, T. Nishimura, H. Makishima,  L. Malcovati, A. Yokoyama, K. Takeuchi, E. Sugihara, T. A. Sato, M. Sanada, A. Takaori-Kondo, M. Cazzola, M. Kengaku, S. Miyano, K. Shirahige, H. I. Suzuki, S. Ogawa

“Combined Cohesin-Runx1 Deficiency Synergistically Perturbs Chromatin Looping and Causes Myelodysplastic Syndromes.”

Cancer Discovery, in press (2020)

14_NatureMaterials_YanBo.png

14. Bo Yang, H. Wolfenson, V. Y. Chung,  N. Nakazawa, S. Liu, J. Hu, R. YJ. Huang,  M. P. Sheetz

“Stopping transformed cancer cell growth by rigidity sensing”

Nature Materials, Vol. 19, 239-250 (2020)

13_eLife_Inaki.png

13. M. Inaki, R. Hatori,  N. Nakazawa, T. Okumura, T. Ishibashi, J. Kikuta, M. Ishii, K. Matsuno, H. Honda

“Chiral cell sliding drives left-right asymmetric organ twisting”

eLIFE, Jun. 12;7 (2018)

12_CellReports_Shimin.jpg

12. S. Le, X. Hu, M. Yao, H. Chen, M. Yu, X. Xu, N. Nakazawa, F. M. Margadant, M.P. Sheetz, J. Yan

“Mechanotransmission and Mechanosensing of Human alpha-Actinin 1”

Cell Reports, Vol. 21, No.10, 2714-2723 (2017)

11_PNAS_Nakazawa.jpg

11. N. Nakazawa, A.R. Sathe, G.V. Shivashankar, and M.P. Sheetz,

“Matrix mechanics controls FHL2 movement to the nucleus to activate p21 expression”

Proc. Natl. Acad. Sci. USA, Vol.113, No.44, E6813-E6822 (2016)

10_Nanoletter_Edna.jpg

10. X. Hu, C. Jing, X. Xu, N. Nakazawa, V. W. Cornish, F. Margadant, M. P. Sheetz,

“Cooperative Vinculin binding to Talin mapped by time resolved super resolution microscopy”

Nano letters, Vol.16, No.7, 4062-4068 (2016)

9_Genetics_Okumura.png

9. T. Okumura, T. Sasamura, M. Inatomi, S. Hozumi, M. Nakamura, R. Hatori, K. Taniguchi, N. Nakazawa, E. Suzuki, R. Maeda, T. Yamakawa, and K. Matsuno

“Genetic analysis of Drosophila Class I Myosin genes in Left-Right asymmetric development.”

Genetics, Vol.199, 1183-1199 (2015)

8_MOD_Hatori.gif

8. R. Hatori, T. Ando, T. Sasamura, N. Nakazawa, M. Nakamura, K. Taniguchi, S. Hozumi, J. Kikuta, M. Ishii, K. Matsuno

“Left-right asymmetry is formed in individual cells by intrinsic cell chirality.”

Mechanisms of Development, Vol.133, 146-162 (2014)

7_MOD_Nakamura.gif

7. M. Nakamura, K. Matsumoto, Y. Iwamoto, T. Muguruma, N. Nakazawa, R. Hatori, K. Taniguchi, R. Maeda, K. Matsuno

“Reduced cell number in the hindgut epithelium disrupts hindgut left–right asymmetry in a mutant of , encoding a RhoGEF, in  embryos.”

Mechanisms of Development, Vol.130, 169-180 (2013)

6_Dev_Dyn_Nakazawa.gif

6. N. Nakazawa, K. Taniguchi, T. Okumura, R. Maeda, and K. Matsuno

“A novel Cre/loxP system for mosaic gene expression in the Drosophila embryo.”

Developmental Dynamics, Vol.241, 965-974 (2012)

5_MOD_Kuroda.gif

5. J. Kuroda, M. Nakamura, M. Yoshida, H. Yamamoto, T. Maeda, K. Taniguchi, N. Nakazawa, R. Hatori, A. Ishio, A. Ozaki, S. Shimaoka, T. Ito, H. Iida, T. Okumura, R. Maeda, K. Matsuno

“Canonical Wnt signaling in the visceral muscle is required for left-right asymmetric development of the midgut.”

Mechanisms of Development, Vol.128, 625-639 (2012)

4_Development_Yamakawa.gif

4. T. Yamakawa, K. Yamada, T. Sasamura, N. Nakazawa, M. Kanai, E. Suzuki, M. E. Fortini, and K. Matsuno

“Deficient Notch signaling associated with neurogenic is compensated for by the unfolded protein response in Drosophila.”

Development, Vol.139, 558-67 (2012)

3_Science_Taniguchi.gif

3. K. Taniguchi, R. Maeda, T. Ando, T. Okumura, N. Nakazawa, R. Hatori, M. Nakamura, S. Hozumi, H. Fujiwara, K. Matsuno

​“Chirality in Planar cell shape contributes to left-right asymmetric epithelial morphogenesis.”

Science, Vol.333, 339-341 (2011)

2_Dev_Biol_Okumura.gif

2. T. Okumura, H. Fujiwara, K. Taniguchi, J. Kuroda, N. Nakazawa, M. Nakamura, R. Hatori, A. Ishio, R. Maeda, K. Matsuno

“Left-right asymmetric morphogenesis of the anterior midgut depends on the activation of a non-muscle myosin II in Drosophila.”

Developmental Biology, Vol.344, 693-706 (2010)

1_Dev_Dyn_Hozumi.gif

1. S. Hozumi, R. Maeda, M. T. Kanai, T. Okumura, K. Taniguchi, Y. Kawakatsu, N. Nakazawa, R. Hatori, and K. Matsuno

“Head region of unconventional Myosin I family members is responsible for the organ-specificity of their roles in left-right polarity in Drosophila.”

Developmental Dynamics, Vol.237, 3528-3537 (2008)

総説論文​(1報)

Logo_FCELL.png

1. N. Nakazawa* and M. Kengaku (*Corresponding author)

“Mechanical regulation of nuclear translocation in migratory neurons”

Frontiers in Cell and Developmental Biology, 8:150 (2020)

プレプリント​(1報)

1. Bo Yang, H. Wolfenson, N. Nakazawa, S. Liu, J. Hu, M. P. Sheetz,

“Stopping transformed cell growth with cytoskeletal proteins: Turning a Devil into an Angel”

bioRxiv, https://doi.org/10.1101/221176 (2018)

招待総説​(3報)

3. 中澤 直高、見学 美根子

“脳発生に寄与するニューロン遊走のメカノバイオロジー”

生体の科学, Vol.70, No.4 (2019)

 

2. 中澤 直高

“留学先における体験談-人間関係にフォーカスして-”

実験医学, Vol.33, No.18 (2015)

 

1. 中澤 直高、 谷口喜一郎、 前田礼男、 安藤格士、 松野健治

“左右非対称な組織形態形成の新たな機構-上皮細胞における平面内細胞形状のキラリティの意義-”

実験医学, Vol.30, No.1, 75-78 (2012)

bottom of page