PMC Links for Gene (Select 30425) - PMC

Chiara Cianciolo Cosentino, Nataliya I. Skrypnyk, Lauren L. Brilli, Takuto Chiba, Tatiana Novitskaya, Clara Woods, James West, Vasiliy N. Korotchenko, Lee McDermott, Billy W. Day, Alan J. Davidson, Raymond C. Harris, Mark P. de Caestecker, Neil A. Hukriede

J Am Soc Nephrol. 2013 May 31; 24(6): 943–953. Published online 2013 Apr 25. doi: 10.1681/ASN.2012111055

PMCID:: PMC3665399

Abstract Article

Select item 33353187.

Pax2 regulates a fadd-dependent molecular switch that drives tissue fusion during eye development

Ishaq A. Viringipurampeer, Todd Ferreira, Shannon DeMaria, Jookyung J. Yoon, Xianghong Shan, Mariya Moosajee, Kevin Gregory-Evans, John Ngai, Cheryl Y. Gregory-Evans

Hum Mol Genet. 2012 May 15; 21(10): 2357–2369. Published online 2012 Feb 21. doi: 10.1093/hmg/dds056

PMCID:: PMC3335318

Abstract Article PDF–560K

Select item 26456738.

Temporally-Controlled Site-Specific Recombination in Zebrafish

Stefan Hans, Jan Kaslin, Dorian Freudenreich, Michael Brand

PLoS One. 2009; 4(2): e4640. Published online 2009 Feb 27. doi: 10.1371/journal.pone.0004640

PMCID:: PMC2645673

Abstract Article PDF–1.3M

Select item 433099.

Midline signaling in the primordium of the zebrafish anterior central nervous system.

K Hatta, A W Püschel, C B Kimmel

Proc Natl Acad Sci U S A. 1994 Mar 15; 91(6): 2061–2065. doi: 10.1073/pnas.91.6.2061

PMCID:: PMC43309

Summary Page Browse PDF–1.6M

Select item 910250310.

A novel de novo missense mutation in EFTUD2 identified by whole‐exome sequencing in mandibulofacial dysostosis with microcephaly

Mei Yang, Yanyan Liu, Ziyuan Lin, Huaqin Sun, Ting Hu

J Clin Lab Anal. 2022 May; 36(5): e24440. Published online 2022 Apr 18. doi: 10.1002/jcla.24440

PMCID:: PMC9102503

Abstract Article PDF–2.0M

Select item 690843111.

Developmentally regulated Tcf7l2 splice variants mediate transcriptional repressor functions during eye formation

Rodrigo M Young, Kenneth B Ewan, Veronica P Ferrer, Miguel L Allende, Jasminka Godovac-Zimmermann, Trevor C Dale, Stephen W Wilson

eLife. 2019; 8: e51447. Published online 2019 Dec 12. doi: 10.7554/eLife.51447

PMCID:: PMC6908431

Abstract Article PDF–2.5M

Select item 462261012.

DNA methylation analysis of Homeobox genes implicates HOXB7 hypomethylation as risk factor for neural tube defects

Anne Rochtus, Benedetta Izzi, Elise Vangeel, Sophie Louwette, Christine Wittevrongel, Diether Lambrechts, Yves Moreau, Raf Winand, Carla Verpoorten, Katrien Jansen, Chris Van Geet, Kathleen Freson

Epigenetics. 2015 Jan; 10(1): 92–101. Published online 2015 Jan 29. doi: 10.1080/15592294.2014.998531

PMCID:: PMC4622610

Abstract Article PDF–416K

Select item 363393113.

Syntaxin 16 Regulates Lumen Formation during Epithelial Morphogenesis

Jae-Joon Jung, Shivangi M. Inamdar, Ajit Tiwari, Ding Ye, Fang Lin, Amit Choudhury

PLoS One. 2013; 8(4): e61857. Published online 2013 Apr 23. doi: 10.1371/journal.pone.0061857

PMCID:: PMC3633931

Abstract Article PDF–7.8M

Select item 354094814.

Regeneration-associated WNT Signaling Is Activated in Long-term Reconstituting AC133^bright Acute Myeloid Leukemia Cells

Alessandro Beghini, Francesca Corlazzoli, Luca Del Giacco, Matteo Re, Francesca Lazzaroni, Matteo Brioschi, Giorgio Valentini, Fulvia Ferrazzi, Anna Ghilardi, Marco Righi, Mauro Turrini, Marco Mignardi, Clara Cesana, Vincenzo Bronte, Mats Nilsson, Enrica Morra, Roberto Cairoli

Neoplasia. 2012 Dec; 14(12): 1236–2124. doi: 10.1593/neo.121480

PMCID:: PMC3540948

Abstract Article PDF–3.2M

Select item 319747315.

Transient knockdown and overexpression reveal a developmental role for the zebrafish enosf1b gene

Steve Finckbeiner, Pin-Joe Ko, Blake Carrington, Raman Sood, Kenneth Gross, Bruce Dolnick, Janice Sufrin, Paul Liu

Cell Biosci. 2011; 1: 32. Published online 2011 Sep 26. doi: 10.1186/2045-3701-1-32

PMCID:: PMC3197473

Abstract Article PDF–3.2M

Select item 278002016.

Formation of the zebrafish midbrain-hindbrain boundary constriction requires laminin-dependent basal constriction

Jennifer H. Gutzman, Ellie G. Graeden, Laura Anne Lowery, Heidi S. Holley, Hazel Sive

Mech Dev. Author manuscript; available in PMC 2009 Nov 20.

Published in final edited form as: Mech Dev. 2008 Nov–Dec; 125(11-12): 974–983. Published online 2008 Jul 18. doi: 10.1016/j.mod.2008.07.004

PMCID:: PMC2780020

Abstract Article PDF–1.7M

Select item 936877317.

Knockout of Katnal2 Leads to Autism-like Behaviors and Developmental Delay in Zebrafish

Jing Zheng, Fei Long, Xu Cao, Bo Xiong, Yu Li

Int J Mol Sci. 2022 Aug; 23(15): 8389. Published online 2022 Jul 29. doi: 10.3390/ijms23158389

PMCID:: PMC9368773

Abstract Article PDF–6.4M

Select item 742664118.

SLC20A1 Is Involved in Urinary Tract and Urorectal Development

Johanna Magdalena Rieke, Rong Zhang, Doreen Braun, Öznur Yilmaz, Anna S. Japp, Filipa M. Lopes, Michael Pleschka, Alina C. Hilger, Sophia Schneider, William G. Newman, Glenda M. Beaman, Agneta Nordenskjöld, Anne-Karoline Ebert, Martin Promm, Wolfgang H. Rösch, Raimund Stein, Karin Hirsch, Frank-Mattias Schäfer, Eberhard Schmiedeke, Thomas M. Boemers, Martin Lacher, Dietrich Kluth, Jan-Hendrik Gosemann, Magnus Anderberg, Gillian Barker, Gundela Holmdahl, Göran Läckgren, David Keene, Raimondo M. Cervellione, Elisa Giorgio, Massimo Di Grazia, Wouter F. J. Feitz, Carlo L. M. Marcelis, Iris A. L. M. Van Rooij, Arend Bökenkamp, Goedele M. A. Beckers, Catherine E. Keegan, Amit Sharma, Tikam Chand Dakal, Lars Wittler, Phillip Grote, Nadine Zwink, Ekkehart Jenetzky, Alfredo Brusco, Holger Thiele, Michael Ludwig, Ulrich Schweizer, Adrian S. Woolf, Benjamin Odermatt, Heiko Reutter

Front Cell Dev Biol. 2020; 8: 567. Published online 2020 Aug 7. doi: 10.3389/fcell.2020.00567

PMCID:: PMC7426641

Abstract Article PDF–2.8M

Select item 673694919.

Functional analysis of new human Bardet-Biedl syndrome loci specific variants in the zebrafish model

Sheila Castro-Sánchez, Paula Suarez-Bregua, Rossina Novas, María Álvarez-Satta, Jose L. Badano, Josep Rotllant, Diana Valverde

Sci Rep. 2019; 9: 12936. Published online 2019 Sep 10. doi: 10.1038/s41598-019-49217-7

Correction in:: Sci Rep. 2020; 10: 2876.

PMCID:: PMC6736949

Abstract Article PDF–3.5M

Select item 650686320.

Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction

Caroline M. Kolvenbach, Gabriel C. Dworschak, Sandra Frese, Anna S. Japp, Peggy Schuster, Nina Wenzlitschke, Öznur Yilmaz, Filipa M. Lopes, Alexey Pryalukhin, Luca Schierbaum, Loes F.M. van der Zanden, Franziska Kause, Ronen Schneider, Katarzyna Taranta-Janusz, Maria Szczepańska, Krzysztof Pawlaczyk, William G. Newman, Glenda M. Beaman, Helen M. Stuart, Raimondo M. Cervellione, Wouter F.J. Feitz, Iris A.L.M. van Rooij, Michiel F. Schreuder, Martijn Steffens, Stefanie Weber, Waltraut M. Merz, Markus Feldkötter, Bernd Hoppe, Holger Thiele, Janine Altmüller, Christoph Berg, Glen Kristiansen, Michael Ludwig, Heiko Reutter, Adrian S. Woolf, Friedhelm Hildebrandt, Phillip Grote, Marcin Zaniew, Benjamin Odermatt, Alina C. Hilger

Am J Hum Genet. 2019 May 2; 104(5): 994–1006. Published online 2019 May 2. doi: 10.1016/j.ajhg.2019.03.023

PMCID:: PMC6506863

Abstract Article PDF–2.5M

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