Tsuji-Hosokawa A - Search Results

1

Human SRY Expression at the Sex-determining Period is Insufficient to Drive Testis Development in Mice.

Tsuji-Hosokawa A, Ogawa Y, Tsuchiya I, Terao M, Takada S. Tsuji-Hosokawa A, et al. Endocrinology. 2022 Jan 1;163(1):bqab217. doi: 10.1210/endocr/bqab217. Endocrinology. 2022. PMID: 34662386

2

Pulmonary vascular dysfunction in metabolic syndrome.

Willson C, Watanabe M, Tsuji-Hosokawa A, Makino A. Willson C, et al. J Physiol. 2019 Feb;597(4):1121-1141. doi: 10.1113/JP275856. Epub 2018 Sep 12. J Physiol. 2019. PMID: 30125956 Free PMC article. Review.

3

HuR/Cx40 downregulation causes coronary microvascular dysfunction in type 2 diabetes.

Si R, Cabrera JTO, Tsuji-Hosokawa A, Guo R, Watanabe M, Gao L, Lee YS, Moon JS, Scott BT, Wang J, Ashton AW, Rao JN, Wang JY, Yuan JX, Makino A. Si R, et al. Among authors: tsuji hosokawa a. JCI Insight. 2021 Nov 8;6(21):e147982. doi: 10.1172/jci.insight.147982. JCI Insight. 2021. PMID: 34747371 Free PMC article.

4

Peptidyl arginine deiminase 2 (Padi2) is expressed in Sertoli cells in a specific manner and regulated by SOX9 during testicular development.

Tsuji-Hosokawa A, Kashimada K, Kato T, Ogawa Y, Nomura R, Takasawa K, Lavery R, Coschiera A, Schlessinger D, Harley VR, Takada S, Morio T. Tsuji-Hosokawa A, et al. Sci Rep. 2018 Sep 5;8(1):13263. doi: 10.1038/s41598-018-31376-8. Sci Rep. 2018. PMID: 30185873 Free PMC article.

5

Nr5a1 suppression during the murine fetal period optimizes ovarian development by fine-tuning Notch signaling.

Nomura R, Kashimada K, Suzuki H, Zhao L, Tsuji-Hosokawa A, Yagita H, Takagi M, Kanai Y, Bowles J, Koopman P, Kanai-Azuma M, Morio T. Nomura R, et al. J Cell Sci. 2019 Apr 15;132(8):jcs223768. doi: 10.1242/jcs.223768. J Cell Sci. 2019. PMID: 30877223

6

Humanization of a tandem repeat in IG-DMR causes stochastic restoration of paternal imprinting at mouse Dlk1-Dio3 domain.

Hara S, Terao M, Tsuji-Hosokawa A, Ogawa Y, Takada S. Hara S, et al. Among authors: tsuji hosokawa a. Hum Mol Genet. 2021 May 12;30(7):564-574. doi: 10.1093/hmg/ddab071. Hum Mol Genet. 2021. PMID: 33709141 Free PMC article.

7

Two ovarian candidate enhancers, identified by time series enhancer RNA analyses, harbor rare genetic variations identified in ovarian insufficiency.

Nakagawa R, Takasawa K, Gau M, Tsuji-Hosokawa A, Kawaji H, Murakawa Y, Takada S, Mikami M, Narumi S, Fukami M, Sreenivasan R, Maruyama T, Tucker EJ, Zhao L, Bowles J, Sinclair A, Koopman P, Hayashizaki Y, Morio T, Kashimada K. Nakagawa R, et al. Among authors: tsuji hosokawa a. Hum Mol Genet. 2022 Jul 7;31(13):2223-2235. doi: 10.1093/hmg/ddac023. Hum Mol Genet. 2022. PMID: 35134173

8

SOX9 and SRY binding sites on mouse mXYSRa/Enh13 enhancer redundantly regulate Sox9 expression to varying degrees.

Ogawa Y, Terao M, Tsuji-Hosokawa A, Tsuchiya I, Hasegawa M, Takada S. Ogawa Y, et al. Among authors: tsuji hosokawa a. Hum Mol Genet. 2023 Jan 1;32(1):55-64. doi: 10.1093/hmg/ddac184. Hum Mol Genet. 2023. PMID: 35921234

9

The progression of salt-wasting and the body weight change during the first 2 weeks of life in classical 21-hydroxylase deficiency patients.

Gau M, Konishi K, Takasawa K, Nakagawa R, Tsuji-Hosokawa A, Hashimoto A, Sutani A, Tajima T, Hasegawa T, Morio T, Kashimada K. Gau M, et al. Clin Endocrinol (Oxf). 2021 Feb;94(2):229-236. doi: 10.1111/cen.14347. Epub 2020 Oct 20. Clin Endocrinol (Oxf). 2021. PMID: 33001476

10

The High Relevance of 21-Deoxycortisol, (Androstenedione + 17α-Hydroxyprogesterone)/Cortisol, and 11-Deoxycortisol/17α-Hydroxyprogesterone for Newborn Screening of 21-Hydroxylase Deficiency.

Watanabe K, Tsuji-Hosokawa A, Hashimoto A, Konishi K, Ishige N, Yajima H, Sutani A, Nakatani H, Gau M, Takasawa K, Tajima T, Hasegawa T, Morio T, Kashimada K. Watanabe K, et al. Among authors: tsuji hosokawa a. J Clin Endocrinol Metab. 2022 Nov 25;107(12):3341-3352. doi: 10.1210/clinem/dgac521. J Clin Endocrinol Metab. 2022. PMID: 36071550

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