Hammerschmidt M - Search Results

1

Essential role of BCL9-2 in the switch between beta-catenin's adhesive and transcriptional functions.

Brembeck FH, Schwarz-Romond T, Bakkers J, Wilhelm S, Hammerschmidt M, Birchmeier W. Brembeck FH, et al. Among authors: hammerschmidt m. Genes Dev. 2004 Sep 15;18(18):2225-30. doi: 10.1101/gad.317604. Epub 2004 Sep 1. Genes Dev. 2004. PMID: 15371335 Free PMC article.

2

Protein kinase A is a common negative regulator of Hedgehog signaling in the vertebrate embryo.

Hammerschmidt M, Bitgood MJ, McMahon AP. Hammerschmidt M, et al. Genes Dev. 1996 Mar 15;10(6):647-58. doi: 10.1101/gad.10.6.647. Genes Dev. 1996. PMID: 8598293 Free article.

3

Genetic analysis of dorsoventral pattern formation in the zebrafish: requirement of a BMP-like ventralizing activity and its dorsal repressor.

Hammerschmidt M, Serbedzija GN, McMahon AP. Hammerschmidt M, et al. Genes Dev. 1996 Oct 1;10(19):2452-61. doi: 10.1101/gad.10.19.2452. Genes Dev. 1996. PMID: 8843197 Free article.

4

Essential role of Bmp7 (snailhouse) and its prodomain in dorsoventral patterning of the zebrafish embryo.

Dick A, Hild M, Bauer H, Imai Y, Maifeld H, Schier AF, Talbot WS, Bouwmeester T, Hammerschmidt M. Dick A, et al. Among authors: hammerschmidt m. Development. 2000 Jan;127(2):343-54. doi: 10.1242/dev.127.2.343. Development. 2000. PMID: 10603351

5

Morpholino phenocopies of the swirl, snailhouse, somitabun, minifin, silberblick, and pipetail mutations.

Lele Z, Bakkers J, Hammerschmidt M. Lele Z, et al. Among authors: hammerschmidt m. Genesis. 2001 Jul;30(3):190-4. doi: 10.1002/gene.1063. Genesis. 2001. PMID: 11477706 No abstract available.

6

Zebrafish DeltaNp63 is a direct target of Bmp signaling and encodes a transcriptional repressor blocking neural specification in the ventral ectoderm.

Bakkers J, Hild M, Kramer C, Furutani-Seiki M, Hammerschmidt M. Bakkers J, et al. Among authors: hammerschmidt m. Dev Cell. 2002 May;2(5):617-27. doi: 10.1016/s1534-5807(02)00163-6. Dev Cell. 2002. PMID: 12015969 Free article.

7

parachute/n-cadherin is required for morphogenesis and maintained integrity of the zebrafish neural tube.

Lele Z, Folchert A, Concha M, Rauch GJ, Geisler R, Rosa F, Wilson SW, Hammerschmidt M, Bally-Cuif L. Lele Z, et al. Among authors: hammerschmidt m. Development. 2002 Jul;129(14):3281-94. doi: 10.1242/dev.129.14.3281. Development. 2002. PMID: 12091300

8

The ankyrin repeat protein Diversin recruits Casein kinase Iepsilon to the beta-catenin degradation complex and acts in both canonical Wnt and Wnt/JNK signaling.

Schwarz-Romond T, Asbrand C, Bakkers J, Kühl M, Schaeffer HJ, Huelsken J, Behrens J, Hammerschmidt M, Birchmeier W. Schwarz-Romond T, et al. Among authors: hammerschmidt m. Genes Dev. 2002 Aug 15;16(16):2073-84. doi: 10.1101/gad.230402. Genes Dev. 2002. PMID: 12183362 Free PMC article.

9

Has2 is required upstream of Rac1 to govern dorsal migration of lateral cells during zebrafish gastrulation.

Bakkers J, Kramer C, Pothof J, Quaedvlieg NE, Spaink HP, Hammerschmidt M. Bakkers J, et al. Among authors: hammerschmidt m. Development. 2004 Feb;131(3):525-37. doi: 10.1242/dev.00954. Development. 2004. PMID: 14729574

10

Fgf3 signaling from the ventral diencephalon is required for early specification and subsequent survival of the zebrafish adenohypophysis.

Herzog W, Sonntag C, von der Hardt S, Roehl HH, Varga ZM, Hammerschmidt M. Herzog W, et al. Among authors: hammerschmidt m. Development. 2004 Aug;131(15):3681-92. doi: 10.1242/dev.01235. Epub 2004 Jun 30. Development. 2004. PMID: 15229178

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