Geisler R - Search Results

1

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: geisler r. Development. 2003 Oct;130(20):5043-52. doi: 10.1242/dev.00704. Development. 2003. PMID: 12952905

2

Maternal and embryonic expression of zebrafish lef1.

Dorsky RI, Snyder A, Cretekos CJ, Grunwald DJ, Geisler R, Haffter P, Moon RT, Raible DW. Dorsky RI, et al. Among authors: geisler r. Mech Dev. 1999 Aug;86(1-2):147-50. doi: 10.1016/s0925-4773(99)00101-x. Mech Dev. 1999. PMID: 10446273 Free article.

3

Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness.

Ernest S, Rauch GJ, Haffter P, Geisler R, Petit C, Nicolson T. Ernest S, et al. Among authors: geisler r. Hum Mol Genet. 2000 Sep 1;9(14):2189-96. doi: 10.1093/hmg/9.14.2189. Hum Mol Genet. 2000. PMID: 10958658

4

The type I serine/threonine kinase receptor Alk8/Lost-a-fin is required for Bmp2b/7 signal transduction during dorsoventral patterning of the zebrafish embryo.

Bauer H, Lele Z, Rauch GJ, Geisler R, Hammerschmidt M. Bauer H, et al. Among authors: geisler r. Development. 2001 Mar;128(6):849-58. doi: 10.1242/dev.128.6.849. Development. 2001. PMID: 11222140

5

A mutation in the Gsk3-binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon.

Heisenberg CP, Houart C, Take-Uchi M, Rauch GJ, Young N, Coutinho P, Masai I, Caneparo L, Concha ML, Geisler R, Dale TC, Wilson SW, Stemple DL. Heisenberg CP, et al. Among authors: geisler r. Genes Dev. 2001 Jun 1;15(11):1427-34. doi: 10.1101/gad.194301. Genes Dev. 2001. PMID: 11390362 Free PMC article.

6

Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates.

Dutton KA, Pauliny A, Lopes SS, Elworthy S, Carney TJ, Rauch J, Geisler R, Haffter P, Kelsh RN. Dutton KA, et al. Among authors: geisler r. Development. 2001 Nov;128(21):4113-25. doi: 10.1242/dev.128.21.4113. Development. 2001. PMID: 11684650

7

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: geisler r. Development. 2001 Aug;128(16):3081-94. doi: 10.1242/dev.128.16.3081. Development. 2001. PMID: 11688558

8

her1 and the notch pathway function within the oscillator mechanism that regulates zebrafish somitogenesis.

Holley SA, Jülich D, Rauch GJ, Geisler R, Nüsslein-Volhard C. Holley SA, et al. Among authors: geisler r. Development. 2002 Mar;129(5):1175-83. doi: 10.1242/dev.129.5.1175. Development. 2002. PMID: 11874913

9

Retinoic acid signalling in the zebrafish embryo is necessary during pre-segmentation stages to pattern the anterior-posterior axis of the CNS and to induce a pectoral fin bud.

Grandel H, Lun K, Rauch GJ, Rhinn M, Piotrowski T, Houart C, Sordino P, Küchler AM, Schulte-Merker S, Geisler R, Holder N, Wilson SW, Brand M. Grandel H, et al. Among authors: geisler r. Development. 2002 Jun;129(12):2851-65. doi: 10.1242/dev.129.12.2851. Development. 2002. PMID: 12050134

10

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: geisler r. Development. 2002 Jul;129(14):3281-94. doi: 10.1242/dev.129.14.3281. Development. 2002. PMID: 12091300

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