Kinoshita A - Search Results

1

Sonic hedgehog expands neural stem cells in the neocortical region leading to an expanded and wrinkled neocortical surface.

Shqirat M, Kinoshita A, Kageyama R, Ohtsuka T. Shqirat M, et al. Among authors: kinoshita a. Genes Cells. 2021 Jun;26(6):399-410. doi: 10.1111/gtc.12847. Epub 2021 Apr 14. Genes Cells. 2021. PMID: 33811429 Free article.

2

Modification of gene expression and soluble factor secretion in the lateral ventricle choroid plexus: Analysis of the impacts on the neocortical development.

Kinoshita A, Shqirat M, Kageyama R, Ohtsuka T. Kinoshita A, et al. Neurosci Res. 2022 Apr;177:38-51. doi: 10.1016/j.neures.2021.12.005. Epub 2021 Dec 27. Neurosci Res. 2022. PMID: 34968558

3

Role of DNA methylation and histone H3 lysine 27 methylation in tissue-specific imprinting of mouse Grb10.

Yamasaki-Ishizaki Y, Kayashima T, Mapendano CK, Soejima H, Ohta T, Masuzaki H, Kinoshita A, Urano T, Yoshiura K, Matsumoto N, Ishimaru T, Mukai T, Niikawa N, Kishino T. Yamasaki-Ishizaki Y, et al. Among authors: kinoshita a. Mol Cell Biol. 2007 Jan;27(2):732-42. doi: 10.1128/MCB.01329-06. Epub 2006 Nov 13. Mol Cell Biol. 2007. PMID: 17101788 Free PMC article.

4

Itpr1 regulates the formation of anterior eye segment tissues derived from neural crest cells.

Kinoshita A, Ohyama K, Tanimura S, Matsuda K, Kishino T, Negishi Y, Asahina N, Shiraishi H, Hosoki K, Tomiwa K, Ishihara N, Mishima H, Mori R, Nakashima M, Saitoh S, Yoshiura KI. Kinoshita A, et al. Development. 2021 Aug 15;148(16):dev188755. doi: 10.1242/dev.188755. Epub 2021 Aug 26. Development. 2021. PMID: 34338282

5

Developmentally dynamic changes of DNA methylation in the mouse Snurf/Snrpn gene.

Miyazaki K, Mapendano CK, Fuchigami T, Kondo S, Ohta T, Kinoshita A, Tsukamoto K, Yoshiura K, Niikawa N, Kishino T. Miyazaki K, et al. Among authors: kinoshita a. Gene. 2009 Mar 1;432(1-2):97-101. doi: 10.1016/j.gene.2008.11.019. Epub 2008 Nov 27. Gene. 2009. PMID: 19095049

6

Identification of a 3.0-kb major recombination hotspot in patients with Sotos syndrome who carry a common 1.9-Mb microdeletion.

Visser R, Shimokawa O, Harada N, Kinoshita A, Ohta T, Niikawa N, Matsumoto N. Visser R, et al. Among authors: kinoshita a. Am J Hum Genet. 2005 Jan;76(1):52-67. doi: 10.1086/426950. Epub 2004 Nov 16. Am J Hum Genet. 2005. PMID: 15580547 Free PMC article.

7

Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia.

Shimokawa O, Miyake N, Yoshimura T, Sosonkina N, Harada N, Mizuguchi T, Kondoh S, Kishino T, Ohta T, Remco V, Takashima T, Kinoshita A, Yoshiura K, Niikawa N, Matsumoto N. Shimokawa O, et al. Among authors: kinoshita a. Am J Med Genet A. 2005 Jul 1;136(1):49-51. doi: 10.1002/ajmg.a.30778. Am J Med Genet A. 2005. PMID: 15937941

8

The IHPK1 gene is disrupted at the 3p21.31 breakpoint of t(3;9) in a family with type 2 diabetes mellitus.

Kamimura J, Wakui K, Kadowaki H, Watanabe Y, Miyake K, Harada N, Sakamoto M, Kinoshita A, Yoshiura KI, Ohta T, Kishino T, Ishikawa M, Kasuga M, Fukushima Y, Niikawa N, Matsumoto N. Kamimura J, et al. Among authors: kinoshita a. J Hum Genet. 2004;49(7):360-365. doi: 10.1007/s10038-004-0158-z. Epub 2004 Jun 18. J Hum Genet. 2004. PMID: 15221640

9

Congenital arhinia: molecular-genetic analysis of five patients.

Sato D, Shimokawa O, Harada N, Olsen OE, Hou JW, Muhlbauer W, Blinkenberg E, Okamoto N, Kinoshita A, Matsumoto N, Kondo S, Kishino T, Miwa N, Ariga T, Niikawa N, Yoshiura K. Sato D, et al. Among authors: kinoshita a. Am J Med Genet A. 2007 Mar 15;143A(6):546-52. doi: 10.1002/ajmg.a.31613. Am J Med Genet A. 2007. PMID: 17304554

10

The possibility of microarray-based analysis using cell-free placental mRNA in maternal plasma.

Miura K, Miura S, Yamasaki K, Shimada T, Kinoshita A, Niikawa N, Yoshiura K, Masuzaki H. Miura K, et al. Among authors: kinoshita a. Prenat Diagn. 2010 Sep;30(9):849-61. doi: 10.1002/pd.2570. Prenat Diagn. 2010. PMID: 20665716

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