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Items: 13

1.

Correction to ZnO/NiO Diode-Based Charge Trapping Layer for Flash Memory Featuring Low Voltage Operation.

Sun CE, Chen CY, Chu KL, Shen YS, Lin CC, Wu YH.

ACS Appl Mater Interfaces. 2015 May 13;7(18):10067. doi: 10.1021/acsami.5b03117. Epub 2015 Apr 29. No abstract available.

PMID:
25923445
2.

ZnO/NiO diode-based charge-trapping layer for flash memory featuring low-voltage operation.

Sun CE, Chen CY, Chu KL, Shen YS, Lin CC, Wu YH.

ACS Appl Mater Interfaces. 2015 Apr 1;7(12):6383-90. doi: 10.1021/am507535c. Epub 2015 Mar 17. Erratum in: ACS Appl Mater Interfaces. 2015 May 13;7(18):10067.

PMID:
25781005
3.

B-type natriuretic peptide: prognostic marker in congenital diaphragmatic hernia.

Steurer MA, Moon-Grady AJ, Fineman JR, Sun CE, Lusk LA, Wai KC, Keller RL.

Pediatr Res. 2014 Dec;76(6):549-54. doi: 10.1038/pr.2014.136. Epub 2014 Sep 4.

4.

Simplified ZrTiO x -based RRAM cell structure with rectifying characteristics by integrating Ni/nā€‰+ā€‰-Si diode.

Lin CC, Wu YH, Chang YT, Sun CE.

Nanoscale Res Lett. 2014 May 30;9(1):275. doi: 10.1186/1556-276X-9-275. eCollection 2014.

5.

Altered reactivity and nitric oxide signaling in the isolated thoracic duct from an ovine model of congenital heart disease with increased pulmonary blood flow.

Datar SA, Oishi PE, Gong W, Bennett SH, Sun CE, Johengen M, Maki J, Johnson RC, Raff GW, Fineman JR.

Am J Physiol Heart Circ Physiol. 2014 Apr 1;306(7):H954-62. doi: 10.1152/ajpheart.00841.2013. Epub 2014 Feb 14.

7.

The DISABLED protein functions in CLATHRIN-mediated synaptic vesicle endocytosis and exoendocytic coupling at the active zone.

Kawasaki F, Iyer J, Posey LL, Sun CE, Mammen SE, Yan H, Ordway RW.

Proc Natl Acad Sci U S A. 2011 Jun 21;108(25):E222-9. doi: 10.1073/pnas.1102231108. Epub 2011 May 23.

8.

Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation.

Beiraghi S, Miller-Chisholm A, Kimberling WJ, Sun CE, Wang YF, Russell LJ, Khoshnevisan M, Storm AL, Long RE Jr, Witt PD, Mazaheri M, Diehl SR.

J Craniofac Genet Dev Biol. 1999 Jul-Sep;19(3):128-34.

PMID:
10589394
9.

Exclusion of chromosome 7 for Kartagener syndrome but suggestion of linkage in families with other forms of primary ciliary dyskinesia.

Witt M, Wang Yf, Wang S, Sun Ce, Pawlik J, Rutkiewicz E, Zebrak J, Diehl SR.

Am J Hum Genet. 1999 Jan;64(1):313-8. No abstract available.

10.

Evidence of linkage disequilibrium between schizophrenia and the SCa1 CAG repeat on chromosome 6p23.

Wang S, Detera-Wadleigh SD, Coon H, Sun CE, Goldin LR, Duffy DL, Byerley WF, Gershon ES, Diehl SR.

Am J Hum Genet. 1996 Sep;59(3):731-6. No abstract available.

11.

Evidence for a susceptibility locus for schizophrenia on chromosome 6pter-p22.

Wang S, Sun CE, Walczak CA, Ziegle JS, Kipps BR, Goldin LR, Diehl SR.

Nat Genet. 1995 May;10(1):41-6.

PMID:
7647789
12.

[Early secondary thoracotomy in the treatment of intrathoracic esophagogastrostomy leakage].

Sun CE, Zhou SM, Li JC.

Zhonghua Wai Ke Za Zhi. 1985 Feb;23(2):95-6, 127. Chinese. No abstract available.

PMID:
3987472
13.

Incontinentia pigmenti.

TEIK KO, SMITH GD, SUN CE.

Med J Malaya. 1959 Sep;14:17-26. No abstract available.

PMID:
13837285

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