Schilling TF - Search Results

1

Combinatorial roles for BMPs and Endothelin 1 in patterning the dorsal-ventral axis of the craniofacial skeleton.

Alexander C, Zuniga E, Blitz IL, Wada N, Le Pabic P, Javidan Y, Zhang T, Cho KW, Crump JG, Schilling TF. Alexander C, et al. Among authors: schilling tf. Development. 2011 Dec;138(23):5135-46. doi: 10.1242/dev.067801. Epub 2011 Oct 26. Development. 2011. PMID: 22031543 Free PMC article.

2

Structure of the zebrafish snail1 gene and its expression in wild-type, spadetail and no tail mutant embryos.

Thisse C, Thisse B, Schilling TF, Postlethwait JH. Thisse C, et al. Among authors: schilling tf. Development. 1993 Dec;119(4):1203-15. doi: 10.1242/dev.119.4.1203. Development. 1993. PMID: 8306883

3

The chinless mutation and neural crest cell interactions in zebrafish jaw development.

Schilling TF, Walker C, Kimmel CB. Schilling TF, et al. Development. 1996 May;122(5):1417-26. doi: 10.1242/dev.122.5.1417. Development. 1996. PMID: 8625830

4

Musculoskeletal patterning in the pharyngeal segments of the zebrafish embryo.

Schilling TF, Kimmel CB. Schilling TF, et al. Development. 1997 Aug;124(15):2945-60. doi: 10.1242/dev.124.15.2945. Development. 1997. PMID: 9247337

5

sucker encodes a zebrafish Endothelin-1 required for ventral pharyngeal arch development.

Miller CT, Schilling TF, Lee K, Parker J, Kimmel CB. Miller CT, et al. Among authors: schilling tf. Development. 2000 Sep;127(17):3815-28. doi: 10.1242/dev.127.17.3815. Development. 2000. PMID: 10934026

6

The zebrafish neckless mutation reveals a requirement for raldh2 in mesodermal signals that pattern the hindbrain.

Begemann G, Schilling TF, Rauch GJ, Geisler R, Ingham PW. Begemann G, et al. Among authors: schilling tf. Development. 2001 Aug;128(16):3081-94. doi: 10.1242/dev.128.16.3081. Development. 2001. PMID: 11688558

7

Requirement for endoderm and FGF3 in ventral head skeleton formation.

David NB, Saint-Etienne L, Tsang M, Schilling TF, Rosa FM. David NB, et al. Among authors: schilling tf. Development. 2002 Oct;129(19):4457-68. doi: 10.1242/dev.129.19.4457. Development. 2002. PMID: 12223404

8

The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans.

Piotrowski T, Ahn DG, Schilling TF, Nair S, Ruvinsky I, Geisler R, Rauch GJ, Haffter P, Zon LI, Zhou Y, Foott H, Dawid IB, Ho RK. Piotrowski T, et al. Among authors: schilling tf. Development. 2003 Oct;130(20):5043-52. doi: 10.1242/dev.00704. Development. 2003. PMID: 12952905

9

lockjaw encodes a zebrafish tfap2a required for early neural crest development.

Knight RD, Nair S, Nelson SS, Afshar A, Javidan Y, Geisler R, Rauch GJ, Schilling TF. Knight RD, et al. Among authors: schilling tf. Development. 2003 Dec;130(23):5755-68. doi: 10.1242/dev.00575. Epub 2003 Oct 8. Development. 2003. PMID: 14534133

10

Skeletal and pigment cell defects in the lockjaw mutant reveal multiple roles for zebrafish tfap2a in neural crest development.

Knight RD, Javidan Y, Nelson S, Zhang T, Schilling T. Knight RD, et al. Dev Dyn. 2004 Jan;229(1):87-98. doi: 10.1002/dvdy.10494. Dev Dyn. 2004. PMID: 14699580 Free article.

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