Medaka spalt acts as a target gene of hedgehog signaling

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				A. Herpin, S. Nakamura, T. U. Wagner, M. Tanaka, and M. Schartl A highly conserved cis-regulatory motif directs differential gonadal synexpression of Dmrt1 transcripts during gonad development Nucleic Acids Res., April 1, 2009; 37(5): 1510 - 1520. [Abstract] [Full Text] [PDF]

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				S. J. Harrison, R. Nishinakamura, and A. P. Monaghan Sall1 Regulates Mitral Cell Development and Olfactory Nerve Extension in the Developing Olfactory Bulb Cereb Cortex, July 1, 2008; 18(7): 1604 - 1617. [Abstract] [Full Text] [PDF]

				L. Chai, J. Yang, C. Di, W. Cui, K. Kawakami, R. Lai, and Y. Ma Transcriptional Activation of the SALL1 by the Human SIX1 Homeodomain during Kidney Development J. Biol. Chem., July 14, 2006; 281(28): 18918 - 18926. [Abstract] [Full Text] [PDF]

				R. W. Koster and S. E. Fraser FGF signaling mediates regeneration of the differentiating cerebellum through repatterning of the anterior hindbrain and reinitiation of neuronal migration. J. Neurosci., July 5, 2006; 26(27): 7293 - 7304. [Abstract] [Full Text] [PDF]

				J. Ninkovic, A. Tallafuss, C. Leucht, J. Topczewski, B. Tannhauser, L. Solnica-Krezel, and L. Bally-Cuif Inhibition of neurogenesis at the zebrafish midbrain-hindbrain boundary by the combined and dose-dependent activity of a new hairy/E(spl) gene pair Development, January 1, 2005; 132(1): 75 - 88. [Abstract] [Full Text] [PDF]

				W Borozdin, D Boehm, M Leipoldt, C Wilhelm, W Reardon, J Clayton-Smith, K Becker, H Muhlendyck, R Winter, O Giray, et al. SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism J. Med. Genet., September 1, 2004; 41(9): e113 - e113. [Full Text] [PDF]

				M. Parrish, T. Ott, C. Lance-Jones, G. Schuetz, A. Schwaeger-Nickolenko, and A. P. Monaghan Loss of the Sall3 Gene Leads to Palate Deficiency, Abnormalities in Cranial Nerves, and Perinatal Lethality Mol. Cell. Biol., August 15, 2004; 24(16): 7102 - 7112. [Abstract] [Full Text] [PDF]

				D. Li, Y. Tian, Y. Ma, and T. Benjamin p150Sal2 Is a p53-Independent Regulator of p21WAF1/CIP Mol. Cell. Biol., May 1, 2004; 24(9): 3885 - 3893. [Abstract] [Full Text] [PDF]

				J. Jaszai, F. Reifers, A. Picker, T. Langenberg, and M. Brand Isthmus-to-midbrain transformation in the absence of midbrain-hindbrain organizer activity Development, December 29, 2003; 130(26): 6611 - 6623. [Abstract] [Full Text] [PDF]

				S. M. Kiefer, K. K. Ohlemiller, J. Yang, B. W. McDill, J. Kohlhase, and M. Rauchman Expression of a truncated Sall1 transcriptional repressor is responsible for Townes-Brocks syndrome birth defects Hum. Mol. Genet., September 1, 2003; 12(17): 2221 - 2227. [Abstract] [Full Text] [PDF]

				J Kohlhase, L Schubert, M Liebers, A Rauch, K Becker, S N Mohammed, R Newbury-Ecob, and W Reardon Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy J. Med. Genet., July 1, 2003; 40(7): 473 - 478. [Abstract] [Full Text] [PDF]

				G. Reim and M. Brand spiel-ohne-grenzen/pou2 mediates regional competence to respond to Fgf8 during zebrafish early neural development Development, March 4, 2003; 129(4): 917 - 933. [Abstract] [Full Text] [PDF]

				D. Sweetman, T. Smith, E. R. Farrell, A. Chantry, and A. Munsterberg The Conserved Glutamine-rich Region of Chick Csal1 and Csal3 Mediates Protein Interactions with Other Spalt Family Members. IMPLICATIONS FOR TOWNES-BROCKS SYNDROME J. Biol. Chem., February 14, 2003; 278(8): 6560 - 6566. [Abstract] [Full Text] [PDF]

				M. Carl, F. Loosli, and J. Wittbrodt Six3 inactivation reveals its essential role for the formation and patterning of the vertebrate eye Development, September 1, 2002; 129(17): 4057 - 4063. [Abstract] [Full Text] [PDF]

				Y. Ma, D. Li, L. Chai, A. M. Luciani, D. Ford, J. Morgan, and A. L. Maizel Cloning and Characterization of Two Promoters for the Human HSAL2 Gene and Their Transcriptional Repression by the Wilms Tumor Suppressor Gene Product J. Biol. Chem., December 14, 2001; 276(51): 48223 - 48230. [Abstract] [Full Text] [PDF]

				C. Netzer, L. Rieger, A. Brero, C.-D. Zhang, M. Hinzke, J. Kohlhase, and S. K. Bohlander SALL1, the gene mutated in Townes-Brocks syndrome, encodes a transcriptional repressor which interacts with TRF1/PIN2 and localizes to pericentromeric heterochromatin Hum. Mol. Genet., December 1, 2001; 10(26): 3017 - 3024. [Abstract] [Full Text] [PDF]

				T. Rusten, R Cantera, J Urban, G Technau, F. Kafatos, and R Barrio Spalt modifies EGFR-mediated induction of chordotonal precursors in the embryonic PNS of Drosophila promoting the development of oenocytes Development, January 3, 2001; 128(5): 711 - 722. [Abstract] [PDF]

				S Winkler, F Loosli, T Henrich, Y Wakamatsu, and J Wittbrodt The conditional medaka mutation eyeless uncouples patterning and morphogenesis of the eye Development, January 5, 2000; 127(9): 1911 - 1919. [Abstract] [PDF]

				F. Loosli, S. Winkler, and J. Wittbrodt Six3 overexpression initiates the formation of ectopic retina Genes & Dev., March 15, 1999; 13(6): 649 - 654. [Abstract] [Full Text]

				M Carl and J Wittbrodt Graded interference with FGF signalling reveals its dorsoventral asymmetry at the mid-hindbrain boundary Development, January 12, 1999; 126(24): 5659 - 5667. [Abstract] [PDF]

				F Ristoratore, M Carl, K Deschet, L Richard-Parpaillon, D Boujard, J Wittbrodt, D Chourrout, F Bourrat, and J. Joly The midbrain-hindbrain boundary genetic cascade is activated ectopically in the diencephalon in response to the widespread expression of one of its components, the medaka gene Ol-eng2 Development, January 9, 1999; 126(17): 3769 - 3779. [Abstract] [PDF]

				J. de Celis, R Barrio, and F. Kafatos Regulation of the spalt/spalt-related gene complex and its function during sensory organ development in the Drosophila thorax Development, January 6, 1999; 126(12): 2653 - 2662. [Abstract] [PDF]

				K Lun and M Brand A series of no isthmus (noi) alleles of the zebrafish pax2.1 gene reveals multiple signaling events in development of the midbrain-hindbrain boundary Development, January 8, 1998; 125(16): 3049 - 3062. [Abstract] [PDF]