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Items: 11

1.

Correction: A genetically defined asymmetry underlies the inhibitory control of flexor-extensor locomotor movements.

Britz O, Zhang J, Grossmann KS, Dyck J, Kim JC, Dymecki S, Gosgnach S, Goulding M.

Elife. 2015 Nov 25;4:e13038. doi: 10.7554/eLife.13038. No abstract available.

2.

A genetically defined asymmetry underlies the inhibitory control of flexor-extensor locomotor movements.

Britz O, Zhang J, Grossmann KS, Dyck J, Kim JC, Dymecki S, Gosgnach S, Goulding M.

Elife. 2015 Oct 14;4. doi: 10.7554/eLife.04718. Erratum in: Elife. 2015;4:e13038.

3.

Identification of a spinal circuit for light touch and fine motor control.

Bourane S, Grossmann KS, Britz O, Dalet A, Del Barrio MG, Stam FJ, Garcia-Campmany L, Koch S, Goulding M.

Cell. 2015 Jan 29;160(3):503-15. doi: 10.1016/j.cell.2015.01.011.

4.

Shp2/MAPK signaling controls goblet/paneth cell fate decisions in the intestine.

Heuberger J, Kosel F, Qi J, Grossmann KS, Rajewsky K, Birchmeier W.

Proc Natl Acad Sci U S A. 2014 Mar 4;111(9):3472-7. doi: 10.1073/pnas.1309342111. Epub 2014 Feb 18.

5.

Genetic dissection of rhythmic motor networks in mice.

Grossmann KS, Giraudin A, Britz O, Zhang J, Goulding M.

Prog Brain Res. 2010;187:19-37. doi: 10.1016/B978-0-444-53613-6.00002-2.

6.

The tyrosine phosphatase Shp2 in development and cancer.

Grossmann KS, Rosário M, Birchmeier C, Birchmeier W.

Adv Cancer Res. 2010;106:53-89. doi: 10.1016/S0065-230X(10)06002-1. Review.

PMID:
20399956
7.

The tyrosine phosphatase Shp2 (PTPN11) directs Neuregulin-1/ErbB signaling throughout Schwann cell development.

Grossmann KS, Wende H, Paul FE, Cheret C, Garratt AN, Zurborg S, Feinberg K, Besser D, Schulz H, Peles E, Selbach M, Birchmeier W, Birchmeier C.

Proc Natl Acad Sci U S A. 2009 Sep 29;106(39):16704-9. doi: 10.1073/pnas.0904336106. Epub 2009 Sep 11.

8.

Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy.

Heuser A, Plovie ER, Ellinor PT, Grossmann KS, Shin JT, Wichter T, Basson CT, Lerman BB, Sasse-Klaassen S, Thierfelder L, MacRae CA, Gerull B.

Am J Hum Genet. 2006 Dec;79(6):1081-8. Epub 2006 Oct 3.

9.

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy.

Gerull B, Heuser A, Wichter T, Paul M, Basson CT, McDermott DA, Lerman BB, Markowitz SM, Ellinor PT, MacRae CA, Peters S, Grossmann KS, Drenckhahn J, Michely B, Sasse-Klaassen S, Birchmeier W, Dietz R, Breithardt G, Schulze-Bahr E, Thierfelder L.

Nat Genet. 2004 Nov;36(11):1162-4. Epub 2004 Oct 17. Erratum in: Nat Genet. 2005 Jan;37(1):106.

PMID:
15489853
10.

Requirement of plakophilin 2 for heart morphogenesis and cardiac junction formation.

Grossmann KS, Grund C, Huelsken J, Behrend M, Erdmann B, Franke WW, Birchmeier W.

J Cell Biol. 2004 Oct 11;167(1):149-60.

11.

Tyrosine kinase receptor RON functions downstream of the erythropoietin receptor to induce expansion of erythroid progenitors.

van den Akker E, van Dijk T, Parren-van Amelsvoort M, Grossmann KS, Schaeper U, Toney-Earley K, Waltz SE, Löwenberg B, von Lindern M.

Blood. 2004 Jun 15;103(12):4457-65. Epub 2004 Feb 24.

PMID:
14982882

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