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Items: 15

1.

50 Years Ago in The Journal of Pediatrics: Survival of Children with Neuroblastoma Treated with Combination Chemotherapy.

Rios X, Heczey AA.

J Pediatr. 2018 Dec;203:233. doi: 10.1016/j.jpeds.2018.06.015. No abstract available.

PMID:
30470379
2.

Application of polymersomes engineered to target p32 protein for detection of small breast tumors in mice.

Simón-Gracia L, Scodeller P, Fuentes SS, Vallejo VG, Ríos X, San Sebastián E, Sidorenko V, Di Silvio D, Suck M, De Lorenzi F, Rizzo LY, von Stillfried S, Kilk K, Lammers T, Moya SE, Teesalu T.

Oncotarget. 2018 Apr 10;9(27):18682-18697. doi: 10.18632/oncotarget.24588. eCollection 2018 Apr 10.

3.

Nine-month clinical outcomes in patients with diabetes treated with polymer-free sirolimus-eluting stents and 6‑month vs. 12‑month dual-antiplatelet therapy (DAPT).

Krackhardt F, Waliszewski M, Rischner J, Piot C, Pansieri M, Ruiz-Poveda FL, Boxberger M, Noutsias M, Ríos XF, Kherad B.

Herz. 2018 Jan 22. doi: 10.1007/s00059-017-4675-x. [Epub ahead of print]

PMID:
29356832
4.

T-Cell Lymphopenia Detected by Newborn Screening in Two Siblings with an Xq13.1 Duplication.

Rios X, Chinn IK, Orange JS, Hanson CI, Rider NL.

Front Pediatr. 2017 Jul 18;5:156. doi: 10.3389/fped.2017.00156. eCollection 2017.

5.

Efficient, footprint-free human iPSC genome editing by consolidation of Cas9/CRISPR and piggyBac technologies.

Wang G, Yang L, Grishin D, Rios X, Ye LY, Hu Y, Li K, Zhang D, Church GM, Pu WT.

Nat Protoc. 2017 Jan;12(1):88-103. doi: 10.1038/nprot.2016.152. Epub 2016 Dec 8.

6.

A general strategy to construct small molecule biosensors in eukaryotes.

Feng J, Jester BW, Tinberg CE, Mandell DJ, Antunes MS, Chari R, Morey KJ, Rios X, Medford JI, Church GM, Fields S, Baker D.

Elife. 2015 Dec 29;4. pii: e10606. doi: 10.7554/eLife.10606.

7.

[Clinical assessment of body hair in Colombian women: determining the cutoff score that defines hirsutism].

Ríos X, Vergara JI, Wandurraga EA, Rey JJ.

Biomedica. 2013 Jul-Sep;33(3):370-4. Spanish.

8.

Highly multiplexed subcellular RNA sequencing in situ.

Lee JH, Daugharthy ER, Scheiman J, Kalhor R, Yang JL, Ferrante TC, Terry R, Jeanty SS, Li C, Amamoto R, Peters DT, Turczyk BM, Marblestone AH, Inverso SA, Bernard A, Mali P, Rios X, Aach J, Church GM.

Science. 2014 Mar 21;343(6177):1360-3. doi: 10.1126/science.1250212. Epub 2014 Feb 27.

9.

Optimization of scarless human stem cell genome editing.

Yang L, Guell M, Byrne S, Yang JL, De Los Angeles A, Mali P, Aach J, Kim-Kiselak C, Briggs AW, Rios X, Huang PY, Daley G, Church G.

Nucleic Acids Res. 2013 Oct;41(19):9049-61. doi: 10.1093/nar/gkt555. Epub 2013 Jul 31.

10.

Whole-exome sequencing enables rapid determination of xeroderma pigmentosum molecular etiology.

Ortega-Recalde O, Vergara JI, Fonseca DJ, Ríos X, Mosquera H, Bermúdez OM, Medina CL, Vargas CI, Pallares AE, Restrepo CM, Laissue P.

PLoS One. 2013 Jun 3;8(6):e64692. doi: 10.1371/journal.pone.0064692. Print 2014.

11.

Genome engineering in Saccharomyces cerevisiae using CRISPR-Cas systems.

DiCarlo JE, Norville JE, Mali P, Rios X, Aach J, Church GM.

Nucleic Acids Res. 2013 Apr;41(7):4336-43. doi: 10.1093/nar/gkt135. Epub 2013 Mar 4.

12.

A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene.

Fonseca DJ, Rojas RF, Vergara JI, Ríos X, Uribe C, Chávez L, Velandia F, Vargas CI, Restrepo CM, Laissue P.

Br J Dermatol. 2013 Feb;168(2):456-8. doi: 10.1111/j.1365-2133.2012.11181.x. No abstract available.

PMID:
22834809
13.

Iterative capped assembly: rapid and scalable synthesis of repeat-module DNA such as TAL effectors from individual monomers.

Briggs AW, Rios X, Chari R, Yang L, Zhang F, Mali P, Church GM.

Nucleic Acids Res. 2012 Aug;40(15):e117. doi: 10.1093/nar/gks624. Epub 2012 Jun 26.

14.

Stable gene targeting in human cells using single-strand oligonucleotides with modified bases.

Rios X, Briggs AW, Christodoulou D, Gorham JM, Seidman JG, Church GM.

PLoS One. 2012;7(5):e36697. doi: 10.1371/journal.pone.0036697. Epub 2012 May 14.

15.

Non-syndromic vestibular disorder with otoconial agenesis in tilted/mergulhador mice caused by mutations in otopetrin 1.

Hurle B, Ignatova E, Massironi SM, Mashimo T, Rios X, Thalmann I, Thalmann R, Ornitz DM.

Hum Mol Genet. 2003 Apr 1;12(7):777-89.

PMID:
12651873

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