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Items: 1 to 20 of 56

1.

Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly.

Alcantara D, Timms AE, Gripp K, Baker L, Park K, Collins S, Cheng C, Stewart F, Mehta SG, Saggar A, Sztriha L, Zombor M, Caluseriu O, Mesterman R, Van Allen MI, Jacquinet A, Ygberg S, Bernstein JA, Wenger AM, Guturu H, Bejerano G, Gomez-Ospina N, Lehman A, Alfei E, Pantaleoni C, Conti V, Guerrini R, Moog U, Graham JM Jr, Hevner R, Dobyns WB, O'Driscoll M, Mirzaa GM.

Brain. 2017 Oct 1;140(10):2610-2622. doi: 10.1093/brain/awx203.

PMID:
28969385
2.

SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activation.

Alcantara D, Elmslie F, Tetreault M, Bareke E, Hartley T; Care4Rare Consortium, Majewski J, Boycott K, Innes AM, Dyment DA, O'Driscoll M.

Hum Mol Genet. 2017 Oct 1;26(19):3713-3721. doi: 10.1093/hmg/ddx256.

PMID:
28934384
3.

Effects of Pulsed Electromagnetic Fields on Breast Cancer Cell Line MCF 7 Using Absorption Spectroscopy.

Alcantara DZ, Soliman IJS, Pobre RF, Naguib RNG.

Anticancer Res. 2017 Jul;37(7):3453-3459.

PMID:
28668834
4.

Between a Pod and a Hard Test: The Deep Evolution of Amoebae.

Kang S, Tice AK, Spiegel FW, Silberman JD, Pánek T, Cepicka I, Kostka M, Kosakyan A, Alcântara DMC, Roger AJ, Shadwick LL, Smirnov A, Kudryavtsev A, Lahr DJG, Brown MW.

Mol Biol Evol. 2017 Sep 1;34(9):2258-2270. doi: 10.1093/molbev/msx162.

PMID:
28505375
5.

Caregiver criticism, help-giving, and the burden of schizophrenia among Mexican American families.

Villalobos BT, Ullman J, Krick TW, Alcántara D, Kopelowicz A, López SR.

Br J Clin Psychol. 2017 Sep;56(3):273-285. doi: 10.1111/bjc.12137. Epub 2017 May 2.

PMID:
28464243
6.

Effect of diterpenoid kaurenoic acid on genotoxicity and cell cycle progression in gastric cancer cell lines.

Cardoso PCDS, Rocha CAMD, Leal MF, Bahia MO, Alcântara DDFÁ, Santos RAD, Gonçalves NDS, Ambrósio SR, Cavalcanti BC, Moreira-Nunes CA, Pessoa CDÓ, Burbano RMR.

Biomed Pharmacother. 2017 May;89:772-780. doi: 10.1016/j.biopha.2017.02.085. Epub 2017 Mar 6.

PMID:
28273639
7.

NAD9/NAD7 (mitochondrial nicotinamide adenine dinucleotide dehydrogenase gene)-A new "Holy Grail" phylogenetic and DNA-barcoding marker for Arcellinida (Amoebozoa)?

Blandenier Q, Lara E, Mitchell EA, Alcantara DM, Siemensma FJ, Todorov M, Lahr DJ.

Eur J Protistol. 2017 Apr;58:175-186. doi: 10.1016/j.ejop.2016.12.002. Epub 2016 Dec 23.

PMID:
28222945
8.

In vitro assessment of the genotoxic and cytotoxic effects of boiled juice (tucupi) from Manihot esculenta Crantz roots.

Cunha LA, Mota TC, Cardoso PC, Alcântara DD, Burbano RM, Guimarães AC, Khayat AS, Rocha CA, Bahia MO.

Genet Mol Res. 2016 Oct 5;15(4). doi: 10.4238/gmr.15048825.

PMID:
27808379
9.

Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.

Bagheri H, Badduke C, Qiao Y, Colnaghi R, Abramowicz I, Alcantara D, Dunham C, Wen J, Wildin RS, Nowaczyk MJ, Eichmeyer J, Lehman A, Maranda B, Martell S, Shan X, Lewis SM, O'Driscoll M, Gregory-Evans CY, Rajcan-Separovic E.

JCI Insight. 2016 Mar 17;1(3):e85461.

10.

Iron oxide nanoparticles as magnetic relaxation switching (MRSw) sensors: Current applications in nanomedicine.

Alcantara D, Lopez S, García-Martin ML, Pozo D.

Nanomedicine. 2016 Jul;12(5):1253-62. doi: 10.1016/j.nano.2016.01.005. Epub 2016 Mar 3. Review.

PMID:
26949164
11.

Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis.

Bennett JT, Tan TY, Alcantara D, Tétrault M, Timms AE, Jensen D, Collins S, Nowaczyk MJM, Lindhurst MJ, Christensen KM, Braddock SR, Brandling-Bennett H, Hennekam RCM, Chung B, Lehman A, Su J, Ng S, Amor DJ; University of Washington Center for Mendelian Genomics; Care4Rare Canada Consortium, Majewski J, Biesecker LG, Boycott KM, Dobyns WB, O'Driscoll M, Moog U, McDonell LM.

Am J Hum Genet. 2016 Mar 3;98(3):579-587. doi: 10.1016/j.ajhg.2016.02.006.

12.

Endothelial differentiation of canine yolk sac cells transduced with VEGF.

Fratini P, Carreira AC, Alcântara D, de Oliveira e Silva FM, Rodrigues MN, Miglino MA.

Res Vet Sci. 2016 Feb;104:71-6. doi: 10.1016/j.rvsc.2015.11.010. Epub 2015 Dec 7.

PMID:
26850540
13.

Identification and Characterization of a Novel Constitutional PIK3CA Mutation in a Child Lacking the Typical Segmental Overgrowth of "PIK3CA-Related Overgrowth Spectrum".

Di Donato N, Rump A, Mirzaa GM, Alcantara D, Oliver A, Schrock E, Dobyns WB, O'Driscoll M.

Hum Mutat. 2016 Mar;37(3):242-5. doi: 10.1002/humu.22933. Epub 2015 Dec 15.

14.

Presence of c.3956delC mutation in familial adenomatous polyposis patients from Brazil.

Moreira-Nunes CA, Alcântara Dd, Lima-Júnior SF, Cavalléro SR, Rey JA, Pinto GR, de Assumpção PP, Burbano RR.

World J Gastroenterol. 2015 Aug 21;21(31):9413-9. doi: 10.3748/wjg.v21.i31.9413.

15.

Molecular imaging of breast cancer: present and future directions.

Alcantara D, Leal MP, García-Bocanegra I, García-Martín ML.

Front Chem. 2014 Dec 18;2:112. doi: 10.3389/fchem.2014.00112. eCollection 2014. Review.

16.

Fluorescent nanoparticle imaging allows noninvasive evaluation of immune cell modulation in esophageal dysplasia.

Habibollahi P, Waldron T, Heidari P, Cho HS, Alcantara D, Josephson L, Wang TC, Rustgi AK, Mahmood U.

Mol Imaging. 2014;13:1-11.

17.

Congenital microcephaly.

Alcantara D, O'Driscoll M.

Am J Med Genet C Semin Med Genet. 2014 Jun;166C(2):124-39. doi: 10.1002/ajmg.c.31397. Epub 2014 May 9. Review.

PMID:
24816482
18.

Cellular responses induced in vitro by pestheic acid, a fungal metabolite, in a gastric adenocarcinoma cell line (PG100).

Sousa JM, Matos LA, Alcântara DF, Ribeiro HF, Santos LS, Oliveira MN, Brito-Junior LC, Khayat AS, Guimarães AC, Cunha LA, Burbano RR, Bahia MO.

Genet Mol Res. 2013 Oct 1;12(4):4106-15. doi: 10.4238/2013.October.1.1.

19.

Embryonic development of chicken (Gallus Gallus Domesticus) from 1st to 19th day-ectodermal structures.

Toledo Fonseca E, De Oliveira Silva FM, Alcântara D, Carvalho Cardoso R, Luís Franciolli A, Sarmento CA, Fratini P, José Piantino Ferreira A, Miglino MA.

Microsc Res Tech. 2013 Dec;76(12):1217-25. doi: 10.1002/jemt.22288. Epub 2013 Sep 5.

PMID:
24019213
20.

Mutations in PIK3R1 cause SHORT syndrome.

Dyment DA, Smith AC, Alcantara D, Schwartzentruber JA, Basel-Vanagaite L, Curry CJ, Temple IK, Reardon W, Mansour S, Haq MR, Gilbert R, Lehmann OJ, Vanstone MR, Beaulieu CL; FORGE Canada Consortium, Majewski J, Bulman DE, O'Driscoll M, Boycott KM, Innes AM.

Am J Hum Genet. 2013 Jul 11;93(1):158-66. doi: 10.1016/j.ajhg.2013.06.005. Epub 2013 Jun 27.

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