Haffter P - 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: haffter p. Development. 2003 Oct;130(20):5043-52. doi: 10.1242/dev.00704. Development. 2003. PMID: 12952905

2

Jaw and branchial arch mutants in zebrafish II: anterior arches and cartilage differentiation.

Piotrowski T, Schilling TF, Brand M, Jiang YJ, Heisenberg CP, Beuchle D, Grandel H, van Eeden FJ, Furutani-Seiki M, Granato M, Haffter P, Hammerschmidt M, Kane DA, Kelsh RN, Mullins MC, Odenthal J, Warga RM, Nüsslein-Volhard C. Piotrowski T, et al. Among authors: haffter p. Development. 1996 Dec;123:345-56. doi: 10.1242/dev.123.1.345. Development. 1996. PMID: 9007254

3

Jaw and branchial arch mutants in zebrafish I: branchial arches.

Schilling TF, Piotrowski T, Grandel H, Brand M, Heisenberg CP, Jiang YJ, Beuchle D, Hammerschmidt M, Kane DA, Mullins MC, van Eeden FJ, Kelsh RN, Furutani-Seiki M, Granato M, Haffter P, Odenthal J, Warga RM, Trowe T, Nüsslein-Volhard C. Schilling TF, et al. Among authors: haffter p. Development. 1996 Dec;123:329-44. doi: 10.1242/dev.123.1.329. Development. 1996. PMID: 9007253

4

cyclops encodes a nodal-related factor involved in midline signaling.

Rebagliati MR, Toyama R, Haffter P, Dawid IB. Rebagliati MR, et al. Among authors: haffter p. Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9932-7. doi: 10.1073/pnas.95.17.9932. Proc Natl Acad Sci U S A. 1998. PMID: 9707578 Free PMC article.

5

The smad5 mutation somitabun blocks Bmp2b signaling during early dorsoventral patterning of the zebrafish embryo.

Hild M, Dick A, Rauch GJ, Meier A, Bouwmeester T, Haffter P, Hammerschmidt M. Hild M, et al. Among authors: haffter p. Development. 1999 May;126(10):2149-59. doi: 10.1242/dev.126.10.2149. Development. 1999. PMID: 10207140

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: haffter p. Development. 2001 Nov;128(21):4113-25. doi: 10.1242/dev.128.21.4113. Development. 2001. PMID: 11684650

7

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: haffter p. Mech Dev. 1999 Aug;86(1-2):147-50. doi: 10.1016/s0925-4773(99)00101-x. Mech Dev. 1999. PMID: 10446273 Free article.

8

Zebrafish nodal-related genes are implicated in axial patterning and establishing left-right asymmetry.

Rebagliati MR, Toyama R, Fricke C, Haffter P, Dawid IB. Rebagliati MR, et al. Among authors: haffter p. Dev Biol. 1998 Jul 15;199(2):261-72. doi: 10.1006/dbio.1998.8935. Dev Biol. 1998. PMID: 9698446 Free article.

9

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: haffter p. Hum Mol Genet. 2000 Sep 1;9(14):2189-96. doi: 10.1093/hmg/9.14.2189. Hum Mol Genet. 2000. PMID: 10958658

10

Leukocyte tyrosine kinase functions in pigment cell development.

Lopes SS, Yang X, Müller J, Carney TJ, McAdow AR, Rauch GJ, Jacoby AS, Hurst LD, Delfino-Machín M, Haffter P, Geisler R, Johnson SL, Ward A, Kelsh RN. Lopes SS, et al. Among authors: haffter p. PLoS Genet. 2008 Mar 7;4(3):e1000026. doi: 10.1371/journal.pgen.1000026. PLoS Genet. 2008. PMID: 18369445 Free PMC article.

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