Tsurusaki Y - Search Results

1

Dietary Sodium Nitrite Causes Similar Modifications to Splenic Inflammatory Gene Expression as a High-Fat Diet.

Oarada M, Okumura Y, Hirasaka K, Sugiura K, Tachibana N, Tsurusaki Y, Nikawa T. Oarada M, et al. Among authors: tsurusaki y. J Nutr Sci Vitaminol (Tokyo). 2021;67(6):404-416. doi: 10.3177/jnsv.67.404. J Nutr Sci Vitaminol (Tokyo). 2021. PMID: 34980719 Free article.

2

Whole-exome sequencing reveals the subclonal expression of NUP214-ABL1 fusion gene in T-cell acute lymphoblastic leukemia.

Tsurusaki Y, Nagai JI, Fujita S, Sugiyama M, Nakamura W, Hayashi A, Miyagawa N, Keino D, Yokosuka T, Iwasaki F, Hamanoue S, Shiomi M, Goto S, Kurosawa K, Goto H. Tsurusaki Y, et al. Pediatr Blood Cancer. 2020 Jan;67(1):e28019. doi: 10.1002/pbc.28019. Epub 2019 Sep 25. Pediatr Blood Cancer. 2020. PMID: 31556219 No abstract available.

3

Hemoglobin beta Kanagawa [c.443A>C; p.(Ter148Serext*21)]: A novel β-globin gene mutation causing dominantly inherited β-thalassemia.

Sugiyama M, Hamanoue S, Nagai JI, Tsurusaki Y, Kurosawa K, Tanaka M, Tanaka Y, Goto H. Sugiyama M, et al. Among authors: tsurusaki y. Pediatr Blood Cancer. 2019 Sep;66(9):e27871. doi: 10.1002/pbc.27871. Epub 2019 Jun 3. Pediatr Blood Cancer. 2019. PMID: 31157496 No abstract available.

4

An efficient genetic test flow for multiple congenital anomalies and intellectual disability.

Yokoi T, Enomoto Y, Tsurusaki Y, Harada N, Saito T, Nagai JI, Naruto T, Kurosawa K. Yokoi T, et al. Among authors: tsurusaki y. Pediatr Int. 2020 May;62(5):556-561. doi: 10.1111/ped.14159. Pediatr Int. 2020. PMID: 31955471

5

Novel AMER1 frameshift mutation in a girl with osteopathia striata with cranial sclerosis.

Enomoto Y, Tsurusaki Y, Harada N, Aida N, Kurosawa K. Enomoto Y, et al. Among authors: tsurusaki y. Congenit Anom (Kyoto). 2018 Jul;58(4):145-146. doi: 10.1111/cga.12258. Epub 2017 Nov 16. Congenit Anom (Kyoto). 2018. PMID: 28990699 No abstract available.

6

A female patient with X-linked Ohdo syndrome of the Maat-Kievit-Brunner phenotype caused by a novel variant of MED12.

Murakami H, Enomoto Y, Tsurusaki Y, Sugio Y, Kurosawa K. Murakami H, et al. Among authors: tsurusaki y. Congenit Anom (Kyoto). 2020 May;60(3):91-93. doi: 10.1111/cga.12350. Epub 2019 Jul 29. Congenit Anom (Kyoto). 2020. PMID: 31322785 No abstract available.

7

CNV analysis using whole exome sequencing identified biallelic CNVs of VPS13B in siblings with intellectual disability.

Enomoto Y, Tsurusaki Y, Yokoi T, Abe-Hatano C, Ida K, Naruto T, Mitsui J, Tsuji S, Morishita S, Kurosawa K. Enomoto Y, et al. Among authors: tsurusaki y. Eur J Med Genet. 2020 Jan;63(1):103610. doi: 10.1016/j.ejmg.2018.12.015. Epub 2018 Dec 30. Eur J Med Genet. 2020. PMID: 30602132

8

Kuroda Y, Murakami H, Yokoi T, Kumaki T, Enomoto Y, Tsurusaki Y, Kurosawa K. Kuroda Y, et al. Among authors: tsurusaki y. Brain Dev. 2019 Jun;41(6):538-541. doi: 10.1016/j.braindev.2019.02.007. Epub 2019 Feb 20. Brain Dev. 2019. PMID: 30795918

9

Siblings with vascular Ehlers-Danlos syndrome inherited via maternal mosaicism.

Yokoi T, Enomoto Y, Tsurusaki Y, Kurosawa K. Yokoi T, et al. Among authors: tsurusaki y. Congenit Anom (Kyoto). 2021 May;61(3):101-102. doi: 10.1111/cga.12408. Epub 2021 Jan 31. Congenit Anom (Kyoto). 2021. PMID: 33368646 No abstract available.

10

A novel gene (FAM20B encoding glycosaminoglycan xylosylkinase) for neonatal short limb dysplasia resembling Desbuquois dysplasia.

Kuroda Y, Murakami H, Enomoto Y, Tsurusaki Y, Takahashi K, Mitsuzuka K, Ishimoto H, Nishimura G, Kurosawa K. Kuroda Y, et al. Among authors: tsurusaki y. Clin Genet. 2019 Jun;95(6):713-717. doi: 10.1111/cge.13530. Epub 2019 Apr 11. Clin Genet. 2019. PMID: 30847897

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

219 results

Search Page

Filters