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Items: 1 to 20 of 775

1.

[Detection of TSC1/TSC2 gene mutations among patients with tuberous sclerosis complex by Ion Torrent semiconductor sequencing].

Wang Y, Lin Y, Luo C, Liang D, Ji X, Jiang T, Ma D, Xu Z.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Apr;33(2):169-72. doi: 10.3760/cma.j.issn.1003-9406.2016.02.009. Chinese.

PMID:
27060308
2.

Lysosomal recruitment of TSC2 is a universal response to cellular stress.

Demetriades C, Plescher M, Teleman AA.

Nat Commun. 2016 Feb 12;7:10662. doi: 10.1038/ncomms10662.

3.

Protein kinase D1 inhibits breast cancer cell invasion via regulating matrix metalloproteinase expression.

Qin XJ, Gao ZG, Huan JL, Pan XF, Zhu L.

Eur J Gynaecol Oncol. 2015;36(6):690-3.

PMID:
26775353
4.

Cell line modeling to study biomarker panel in prostate cancer.

NickKholgh B, Fang X, Winters SM, Raina A, Pandya KS, Gyabaah K, Fino N, Balaji KC.

Prostate. 2016 Feb 15;76(3):245-58. doi: 10.1002/pros.23116. Epub 2015 Nov 2.

5.
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The variant Polycomb Repressor Complex 1 component PCGF1 interacts with a pluripotency sub-network that includes DPPA4, a regulator of embryogenesis.

Oliviero G, Munawar N, Watson A, Streubel G, Manning G, Bardwell V, Bracken AP, Cagney G.

Sci Rep. 2015 Dec 21;5:18388. doi: 10.1038/srep18388.

7.

Detection of low-prevalence somatic TSC2 mutations in sporadic pulmonary lymphangioleiomyomatosis tissues by deep sequencing.

Fujita A, Ando K, Kobayashi E, Mitani K, Okudera K, Nakashima M, Miyatake S, Tsurusaki Y, Saitsu H, Seyama K, Miyake N, Matsumoto N.

Hum Genet. 2016 Jan;135(1):61-8. doi: 10.1007/s00439-015-1611-0. Epub 2015 Nov 12.

PMID:
26563443
8.

Biallelic NTHL1 Mutations in a Woman with Multiple Primary Tumors.

Rivera B, Castellsagué E, Bah I, van Kempen LC, Foulkes WD.

N Engl J Med. 2015 Nov 12;373(20):1985-6. doi: 10.1056/NEJMc1506878. Erratum in: N Engl J Med. 2015 Dec 17;373(25):e33.

9.

Mosaic and Intronic Mutations in TSC1/TSC2 Explain the Majority of TSC Patients with No Mutation Identified by Conventional Testing.

Tyburczy ME, Dies KA, Glass J, Camposano S, Chekaluk Y, Thorner AR, Lin L, Krueger D, Franz DN, Thiele EA, Sahin M, Kwiatkowski DJ.

PLoS Genet. 2015 Nov 5;11(11):e1005637. doi: 10.1371/journal.pgen.1005637. eCollection 2015 Nov.

10.

A human interactome in three quantitative dimensions organized by stoichiometries and abundances.

Hein MY, Hubner NC, Poser I, Cox J, Nagaraj N, Toyoda Y, Gak IA, Weisswange I, Mansfeld J, Buchholz F, Hyman AA, Mann M.

Cell. 2015 Oct 22;163(3):712-23. doi: 10.1016/j.cell.2015.09.053. Epub 2015 Oct 22.

PMID:
26496610
11.

Kelch Domain of Gigaxonin Interacts with Intermediate Filament Proteins Affected in Giant Axonal Neuropathy.

Johnson-Kerner BL, Garcia Diaz A, Ekins S, Wichterle H.

PLoS One. 2015 Oct 13;10(10):e0140157. doi: 10.1371/journal.pone.0140157. eCollection 2015.

12.

PAK2 is an effector of TSC1/2 signaling independent of mTOR and a potential therapeutic target for Tuberous Sclerosis Complex.

Alves MM, Fuhler GM, Queiroz KC, Scholma J, Goorden S, Anink J, Spek CA, Hoogeveen-Westerveld M, Bruno MJ, Nellist M, Elgersma Y, Aronica E, Peppelenbosch MP.

Sci Rep. 2015 Sep 28;5:14534. doi: 10.1038/srep14534.

13.

Intellectual ability in tuberous sclerosis complex correlates with predicted effects of mutations on TSC1 and TSC2 proteins.

Wong HT, McCartney DL, Lewis JC, Sampson JR, Howe CJ, de Vries PJ.

J Med Genet. 2015 Dec;52(12):815-22. doi: 10.1136/jmedgenet-2015-103154. Epub 2015 Sep 25.

PMID:
26408672
14.

DNA Base-Excision Repair Genes OGG1 and NTH1 in Brazilian Lung Cancer Patients.

Couto PG, Bastos-Rodrigues L, Carneiro JG, Guieiro F, Bicalho MA, Leidenz FB, Bicalho AJ, Friedman E, De Marco L.

Mol Diagn Ther. 2015 Dec;19(6):389-95. doi: 10.1007/s40291-015-0164-1.

PMID:
26400813
15.

Shared functional defect in IP₃R-mediated calcium signaling in diverse monogenic autism syndromes.

Schmunk G, Boubion BJ, Smith IF, Parker I, Gargus JJ.

Transl Psychiatry. 2015 Sep 22;5:e643. doi: 10.1038/tp.2015.123.

PMID:
26393489
16.

AKT3 promotes prostate cancer proliferation cells through regulation of Akt, B-Raf, and TSC1/TSC2.

Lin HP, Lin CY, Huo C, Jan YJ, Tseng JC, Jiang SS, Kuo YY, Chen SC, Wang CT, Chan TM, Liou JY, Wang J, Chang WS, Chang CH, Kung HJ, Chuu CP.

Oncotarget. 2015 Sep 29;6(29):27097-112. doi: 10.18632/oncotarget.4553.

17.

Elevated expression of mechanosensory polycystins in human carotid atherosclerotic plaques: association with p53 activation and disease severity.

Varela A, Piperi C, Sigala F, Agrogiannis G, Davos CH, Andri MA, Manopoulos C, Tsangaris S, Basdra EK, Papavassiliou AG.

Sci Rep. 2015 Aug 19;5:13461. doi: 10.1038/srep13461.

18.

[Analysis of TSC gene mutation in a patient with tuberous sclerosis].

Zhang Z, Lyu Y, Mu Y, Yang H, Yang P, Liu Y, Liu L, Chen X, Sui W.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Aug;32(4):506-8. doi: 10.3760/cma.j.issn.1003-9406.2015.04.012. Chinese.

PMID:
26252095
19.

The BioPlex Network: A Systematic Exploration of the Human Interactome.

Huttlin EL, Ting L, Bruckner RJ, Gebreab F, Gygi MP, Szpyt J, Tam S, Zarraga G, Colby G, Baltier K, Dong R, Guarani V, Vaites LP, Ordureau A, Rad R, Erickson BK, Wühr M, Chick J, Zhai B, Kolippakkam D, Mintseris J, Obar RA, Harris T, Artavanis-Tsakonas S, Sowa ME, De Camilli P, Paulo JA, Harper JW, Gygi SP.

Cell. 2015 Jul 16;162(2):425-40. doi: 10.1016/j.cell.2015.06.043.

20.

SR protein kinases promote splicing of nonconsensus introns.

Lipp JJ, Marvin MC, Shokat KM, Guthrie C.

Nat Struct Mol Biol. 2015 Aug;22(8):611-7. doi: 10.1038/nsmb.3057. Epub 2015 Jul 13.

PMID:
26167880
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