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Items: 5

1.

Gene- and tissue-level interactions in normal gastrointestinal development and Hirschsprung disease.

Chatterjee S, Nandakumar P, Auer DR, Gabriel SB, Chakravarti A.

Proc Natl Acad Sci U S A. 2019 Dec 9. pii: 201908756. doi: 10.1073/pnas.1908756116. [Epub ahead of print]

PMID:
31818953
2.

Testing the Ret and Sema3d genetic interaction in mouse enteric nervous system development.

Kapoor A, Auer DR, Lee D, Chatterjee S, Chakravarti A.

Hum Mol Genet. 2017 May 15;26(10):1811-1820. doi: 10.1093/hmg/ddx084.

3.

Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung Disease.

Chatterjee S, Kapoor A, Akiyama JA, Auer DR, Lee D, Gabriel S, Berrios C, Pennacchio LA, Chakravarti A.

Cell. 2016 Oct 6;167(2):355-368.e10. doi: 10.1016/j.cell.2016.09.005. Epub 2016 Sep 29.

4.

Loss of δ-catenin function in severe autism.

Turner TN, Sharma K, Oh EC, Liu YP, Collins RL, Sosa MX, Auer DR, Brand H, Sanders SJ, Moreno-De-Luca D, Pihur V, Plona T, Pike K, Soppet DR, Smith MW, Cheung SW, Martin CL, State MW, Talkowski ME, Cook E, Huganir R, Katsanis N, Chakravarti A.

Nature. 2015 Apr 2;520(7545):51-6. doi: 10.1038/nature14186. Epub 2015 Mar 25.

5.

Generation of a cre recombinase-conditional Nos1ap over-expression transgenic mouse.

Auer DR, Sysa-Shah P, Bedja D, Simmers JL, Pak E, Dutra A, Cohn R, Gabrielson KL, Chakravarti A, Kapoor A.

Biotechnol Lett. 2014 Jun;36(6):1179-85. doi: 10.1007/s10529-014-1473-x. Epub 2014 Feb 22.

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