Anderson KV - Search Results

1

Using genomewide mutagenesis screens to identify the genes required for neural tube closure in the mouse.

Zohn IE, Anderson KV, Niswander L. Zohn IE, et al. Among authors: anderson kv. Birth Defects Res A Clin Mol Teratol. 2005 Sep;73(9):583-90. doi: 10.1002/bdra.20164. Birth Defects Res A Clin Mol Teratol. 2005. PMID: 15971254 Review.

2

The Hectd1 ubiquitin ligase is required for development of the head mesenchyme and neural tube closure.

Zohn IE, Anderson KV, Niswander L. Zohn IE, et al. Among authors: anderson kv. Dev Biol. 2007 Jun 1;306(1):208-21. doi: 10.1016/j.ydbio.2007.03.018. Epub 2007 Mar 20. Dev Biol. 2007. PMID: 17442300 Free PMC article.

3

Phactr4 regulates neural tube and optic fissure closure by controlling PP1-, Rb-, and E2F1-regulated cell-cycle progression.

Kim TH, Goodman J, Anderson KV, Niswander L. Kim TH, et al. Among authors: anderson kv. Dev Cell. 2007 Jul;13(1):87-102. doi: 10.1016/j.devcel.2007.04.018. Dev Cell. 2007. PMID: 17609112 Free article.

4

Tissue morphogenesis and vascular stability require the Frem2 protein, product of the mouse myelencephalic blebs gene.

Timmer JR, Mak TW, Manova K, Anderson KV, Niswander L. Timmer JR, et al. Among authors: anderson kv. Proc Natl Acad Sci U S A. 2005 Aug 16;102(33):11746-50. doi: 10.1073/pnas.0505404102. Epub 2005 Aug 8. Proc Natl Acad Sci U S A. 2005. PMID: 16087869 Free PMC article.

5

p38 and a p38-interacting protein are critical for downregulation of E-cadherin during mouse gastrulation.

Zohn IE, Li Y, Skolnik EY, Anderson KV, Han J, Niswander L. Zohn IE, et al. Among authors: anderson kv. Cell. 2006 Jun 2;125(5):957-69. doi: 10.1016/j.cell.2006.03.048. Cell. 2006. PMID: 16751104 Free article.

6

LDL-receptor-related protein 4 is crucial for formation of the neuromuscular junction.

Weatherbee SD, Anderson KV, Niswander LA. Weatherbee SD, et al. Among authors: anderson kv. Development. 2006 Dec;133(24):4993-5000. doi: 10.1242/dev.02696. Development. 2006. PMID: 17119023

7

A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling.

Weatherbee SD, Niswander LA, Anderson KV. Weatherbee SD, et al. Among authors: anderson kv. Hum Mol Genet. 2009 Dec 1;18(23):4565-75. doi: 10.1093/hmg/ddp422. Epub 2009 Sep 22. Hum Mol Genet. 2009. PMID: 19776033 Free PMC article.

8

Hedgehog signalling in the mouse requires intraflagellar transport proteins.

Huangfu D, Liu A, Rakeman AS, Murcia NS, Niswander L, Anderson KV. Huangfu D, et al. Among authors: anderson kv. Nature. 2003 Nov 6;426(6962):83-7. doi: 10.1038/nature02061. Nature. 2003. PMID: 14603322

9

Hopeful monsters and morphogens at the beach.

Niswander L, Anderson KV. Niswander L, et al. Among authors: anderson kv. Nat Cell Biol. 2002 Nov;4(11):E259-62. doi: 10.1038/ncb1102-e259. Nat Cell Biol. 2002. PMID: 12415285

10

The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation.

Becker-Heck A, Zohn IE, Okabe N, Pollock A, Lenhart KB, Sullivan-Brown J, McSheene J, Loges NT, Olbrich H, Haeffner K, Fliegauf M, Horvath J, Reinhardt R, Nielsen KG, Marthin JK, Baktai G, Anderson KV, Geisler R, Niswander L, Omran H, Burdine RD. Becker-Heck A, et al. Among authors: anderson kv. Nat Genet. 2011 Jan;43(1):79-84. doi: 10.1038/ng.727. Epub 2010 Dec 5. Nat Genet. 2011. PMID: 21131974 Free PMC article.

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