Role of dangling bond centers on radiative recombination processes in porous silicon

1995 ◽  
Vol 67 (10) ◽  
pp. 1396-1398 ◽  
Author(s):  
Yasunori Mochizuki ◽  
Masashi Mizuta
1983 ◽  
Vol 103 ◽  
pp. 199-209 ◽  
Author(s):  
P. J. Storey

The role of resonances in the photoionization cross-sections of ions is discussed in relation to the radiative recombination coefficient. The calculation of dielectronic contributions to the recombination coefficient is reviewed for nebular conditions, and the importance of autoionizing states close to the first ionization threshold is illustrated. For those ions for which dielectronic recombination is not important at nebular temperatures, an assessment of the accuracy of the best available recombination coefficients is given.


2008 ◽  
Vol 1 (1) ◽  
pp. 011701 ◽  
Author(s):  
Yujiro Hayashi ◽  
Kazunori Tanaka ◽  
Tatsushi Akazaki ◽  
Masafumi Jo ◽  
Hidekazu Kumano ◽  
...  

2004 ◽  
Vol 1 (10) ◽  
pp. 2500-2503 ◽  
Author(s):  
B. Monemar ◽  
H. Haratizadeh ◽  
P. P. Paskov ◽  
J. P. Bergman ◽  
E. Valcheva ◽  
...  

2020 ◽  
Vol 102 ◽  
Author(s):  
Yael Laitman ◽  
Shay Tzur ◽  
Ruben Attali ◽  
Amit Tirosh ◽  
Eitan Friedman

Abstract Pheochromocytoma (PCC) is a rare, mostly benign tumour of the adrenal medulla. Hereditary PCC accounts for ~35% of cases and has been associated with germline mutations in several cancer susceptibility genes (e.g., KIF1B, SDHB, VHL, SDHD, RET). We performed whole-exome sequencing in a family with four PCC-affected patients in two consecutive generations and identified a potential novel candidate pathogenic variant in the REXO2 gene that affects splicing (c.531-1G>T (NM 015523.3)), which co-segregated with the phenotype in the family. REXO2 encodes for RNA exonuclease 2 protein and localizes to 11q23, a chromosomal region displaying allelic imbalance in PCC. REXO2 protein has been associated with DNA repair, replication and recombination processes and thus its inactivation may contribute to tumorigenesis. While the study suggests that this novel REXO2 gene variant underlies PCC in this family, additional functional studies are required in order to establish the putative role of the REXO2 gene in PCC predisposition.


2008 ◽  
Vol 19 (S1) ◽  
pp. 316-318
Author(s):  
Mahmood Sabooni ◽  
Morteza Esmaeili ◽  
Hamid Haratizadeh ◽  
Bo Monemar ◽  
Hiroshi Amano

Sign in / Sign up

Export Citation Format

Share Document