Yamagishi H - Search Results

1

A genetic and developmental biological approach for a family with complex congenital heart diseases-evidence of digenic inheritance.

Yoshida Y, Uchida K, Kodo K, Ishizaki-Asami R, Maeda J, Katsumata Y, Yuasa S, Fukuda K, Kosaki K, Watanabe Y, Nakagawa O, Yamagishi H. Yoshida Y, et al. Among authors: yamagishi h. Front Cardiovasc Med. 2023 Apr 25;10:1135141. doi: 10.3389/fcvm.2023.1135141. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37180804 Free PMC article.

2

Phenotypic discordance in monozygotic twins with 22q11.2 deletion.

Yamagishi H, Ishii C, Maeda J, Kojima Y, Matsuoka R, Kimura M, Takao A, Momma K, Matsuo N. Yamagishi H, et al. Am J Med Genet. 1998 Jul 24;78(4):319-21. Am J Med Genet. 1998. PMID: 9714432

3

Ventricular septal defect associated with microdeletions of chromosome 22q11.2.

Yamagishi H, Maeda J, Tokumura M, Yoshiba S, Takahashi E, Fukushima H, Yamagishi C, Matsuo N, Kojima Y. Yamagishi H, et al. Among authors: yamagishi c. Clin Genet. 2000 Dec;58(6):493-6. doi: 10.1034/j.1399-0004.2000.580612.x. Clin Genet. 2000. PMID: 11149621

4

The combinatorial activities of Nkx2.5 and dHAND are essential for cardiac ventricle formation.

Yamagishi H, Yamagishi C, Nakagawa O, Harvey RP, Olson EN, Srivastava D. Yamagishi H, et al. Among authors: yamagishi c. Dev Biol. 2001 Nov 15;239(2):190-203. doi: 10.1006/dbio.2001.0417. Dev Biol. 2001. PMID: 11784028 Free article.

5

Bronchomalacia associated with pulmonary atresia, ventricular septal defect and major aortopulmonary collateral arteries, and chromosome 22q11.2 deletion.

Yamagishi H, Maeda J, Higuchi M, Katada Y, Yamagishi C, Matsuo N, Kojima Y. Yamagishi H, et al. Among authors: yamagishi c. Clin Genet. 2002 Sep;62(3):214-9. doi: 10.1034/j.1399-0004.2002.620305.x. Clin Genet. 2002. PMID: 12220436

6

Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors.

Hu T, Yamagishi H, Maeda J, McAnally J, Yamagishi C, Srivastava D. Hu T, et al. Among authors: yamagishi h, yamagishi c. Development. 2004 Nov;131(21):5491-502. doi: 10.1242/dev.01399. Epub 2004 Oct 6. Development. 2004. PMID: 15469978

7

Tbx1 is regulated by forkhead proteins in the secondary heart field.

Maeda J, Yamagishi H, McAnally J, Yamagishi C, Srivastava D. Maeda J, et al. Among authors: yamagishi h, yamagishi c. Dev Dyn. 2006 Mar;235(3):701-10. doi: 10.1002/dvdy.20686. Dev Dyn. 2006. PMID: 16444712 Free PMC article.

8

Sonic hedgehog is essential for first pharyngeal arch development.

Yamagishi C, Yamagishi H, Maeda J, Tsuchihashi T, Ivey K, Hu T, Srivastava D. Yamagishi C, et al. Among authors: yamagishi h. Pediatr Res. 2006 Mar;59(3):349-54. doi: 10.1203/01.pdr.0000199911.17287.3e. Pediatr Res. 2006. PMID: 16492970

9

Molecular embryology for an understanding of congenital heart diseases.

Yamagishi H, Maeda J, Uchida K, Tsuchihashi T, Nakazawa M, Aramaki M, Kodo K, Yamagishi C. Yamagishi H, et al. Among authors: yamagishi c. Anat Sci Int. 2009 Sep;84(3):88-94. doi: 10.1007/s12565-009-0023-4. Epub 2009 Apr 7. Anat Sci Int. 2009. PMID: 19347680 Review.

10

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling.

Kodo K, Nishizawa T, Furutani M, Arai S, Yamamura E, Joo K, Takahashi T, Matsuoka R, Yamagishi H. Kodo K, et al. Among authors: yamagishi h. Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):13933-8. doi: 10.1073/pnas.0904744106. Epub 2009 Aug 4. Proc Natl Acad Sci U S A. 2009. PMID: 19666519 Free PMC article.

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