PubMed (cited) for id: 605284

Year	Number of Results
1971	1
1994	3
1996	6
1997	2
1998	4
1999	7
2000	8
2001	6
2002	8
2004	1
2005	5
2006	1
2007	2
2008	7
2009	7
2010	1
2012	2
2013	1
2014	1
2017	2
2024	0

1

Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.

Lim JS, Gopalappa R, Kim SH, Ramakrishna S, Lee M, Kim WI, Kim J, Park SM, Lee J, Oh JH, Kim HD, Park CH, Lee JS, Kim S, Kim DS, Han JM, Kang HC, Kim HH, Lee JH. Lim JS, et al. Am J Hum Genet. 2017 Mar 2;100(3):454-472. doi: 10.1016/j.ajhg.2017.01.030. Epub 2017 Feb 16. Am J Hum Genet. 2017. PMID: 28215400 Free PMC article.

2

Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex.

Ercan E, Han JM, Di Nardo A, Winden K, Han MJ, Hoyo L, Saffari A, Leask A, Geschwind DH, Sahin M. Ercan E, et al. J Exp Med. 2017 Mar 6;214(3):681-697. doi: 10.1084/jem.20160446. Epub 2017 Feb 9. J Exp Med. 2017. PMID: 28183733 Free PMC article.

3

Coordinated regulation of protein synthesis and degradation by mTORC1.

Zhang Y, Nicholatos J, Dreier JR, Ricoult SJ, Widenmaier SB, Hotamisligil GS, Kwiatkowski DJ, Manning BD. Zhang Y, et al. Nature. 2014 Sep 18;513(7518):440-3. doi: 10.1038/nature13492. Epub 2014 Jul 13. Nature. 2014. PMID: 25043031 Free PMC article.

4

TORC1-dependent epilepsy caused by acute biallelic Tsc1 deletion in adult mice.

Abs E, Goorden SM, Schreiber J, Overwater IE, Hoogeveen-Westerveld M, Bruinsma CF, Aganović E, Borgesius NZ, Nellist M, Elgersma Y. Abs E, et al. Ann Neurol. 2013 Oct;74(4):569-79. doi: 10.1002/ana.23943. Epub 2013 Sep 10. Ann Neurol. 2013. PMID: 23720219

5

Genome sequencing identifies a basis for everolimus sensitivity.

Iyer G, Hanrahan AJ, Milowsky MI, Al-Ahmadie H, Scott SN, Janakiraman M, Pirun M, Sander C, Socci ND, Ostrovnaya I, Viale A, Heguy A, Peng L, Chan TA, Bochner B, Bajorin DF, Berger MF, Taylor BS, Solit DB. Iyer G, et al. Science. 2012 Oct 12;338(6104):221. doi: 10.1126/science.1226344. Epub 2012 Aug 23. Science. 2012. PMID: 22923433 Free PMC article.

6

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.

Tsai PT, Hull C, Chu Y, Greene-Colozzi E, Sadowski AR, Leech JM, Steinberg J, Crawley JN, Regehr WG, Sahin M. Tsai PT, et al. Nature. 2012 Aug 30;488(7413):647-51. doi: 10.1038/nature11310. Nature. 2012. PMID: 22763451 Free PMC article.

7

Tsc/mTORC1 signaling in oocytes governs the quiescence and activation of primordial follicles.

Adhikari D, Zheng W, Shen Y, Gorre N, Hämäläinen T, Cooney AJ, Huhtaniemi I, Lan ZJ, Liu K. Adhikari D, et al. Hum Mol Genet. 2010 Feb 1;19(3):397-410. doi: 10.1093/hmg/ddp483. Epub 2009 Oct 20. Hum Mol Genet. 2010. PMID: 19843540 Free PMC article.

8

Loss of Tsc1, but not Pten, in renal tubular cells causes polycystic kidney disease by activating mTORC1.

Zhou J, Brugarolas J, Parada LF. Zhou J, et al. Hum Mol Genet. 2009 Nov 15;18(22):4428-41. doi: 10.1093/hmg/ddp398. Epub 2009 Aug 19. Hum Mol Genet. 2009. PMID: 19692352

9

Defects in cell polarity underlie TSC and ADPKD-associated cystogenesis.

Bonnet CS, Aldred M, von Ruhland C, Harris R, Sandford R, Cheadle JP. Bonnet CS, et al. Hum Mol Genet. 2009 Jun 15;18(12):2166-76. doi: 10.1093/hmg/ddp149. Epub 2009 Mar 25. Hum Mol Genet. 2009. PMID: 19321600

10

Focal cortical dysplasia: a genotype-phenotype analysis of polymorphisms and mutations in the TSC genes.

Gumbinger C, Rohsbach CB, Schulze-Bonhage A, Korinthenberg R, Zentner J, Häffner M, Fauser S. Gumbinger C, et al. Epilepsia. 2009 Jun;50(6):1396-408. doi: 10.1111/j.1528-1167.2008.01979.x. Epub 2009 Jan 21. Epilepsia. 2009. PMID: 19175396 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

68 results

Results by year