Profiling of gender-specific gene expression for Trichostrongylus vitrinus (Nematoda: Strongylida) by microarray analysis of expressed sequence tag libraries constructed by suppressive-subtractive hybridisation

2004 ◽  
Vol 34 (5) ◽  
pp. 633-643 ◽  
Author(s):  
Alasdair J. Nisbet ◽  
Robin B. Gasser
Gene ◽  
2004 ◽  
Vol 329 ◽  
pp. 167-185 ◽  
Author(s):  
Gregory R. Burton ◽  
Radhakrishnan Nagarajan ◽  
Charlotte A. Peterson ◽  
Robert E. McGehee

2006 ◽  
Vol 164 ◽  
pp. S46
Author(s):  
Erminio Marafante ◽  
Graziella Cimino-Reale ◽  
Casati Barbara ◽  
Marie Vahter

2009 ◽  
Vol 183 (3) ◽  
pp. 1975-1982 ◽  
Author(s):  
Qingsheng Li ◽  
Anthony J. Smith ◽  
Timothy W. Schacker ◽  
John V. Carlis ◽  
Lijie Duan ◽  
...  

Cells ◽  
2020 ◽  
Vol 9 (7) ◽  
pp. 1579
Author(s):  
Cankut Çubuk ◽  
Fatma E. Can ◽  
María Peña-Chilet ◽  
Joaquín Dopazo

Despite the existence of differences in gene expression across numerous genes between males and females having been known for a long time, these have been mostly ignored in many studies, including drug development and its therapeutic use. In fact, the consequences of such differences over the disease mechanisms or the drug action mechanisms are completely unknown. Here we applied mechanistic mathematical models of signaling activity to reveal the ultimate functional consequences that gender-specific gene expression activities have over cell functionality and fate. Moreover, we also used the mechanistic modeling framework to simulate the drug interventions and unravel how drug action mechanisms are affected by gender-specific differential gene expression. Interestingly, some cancers have many biological processes significantly affected by these gender-specific differences (e.g., bladder or head and neck carcinomas), while others (e.g., glioblastoma or rectum cancer) are almost insensitive to them. We found that many of these gender-specific differences affect cancer-specific pathways or in physiological signaling pathways, also involved in cancer origin and development. Finally, mechanistic models have the potential to be used for finding alternative therapeutic interventions on the pathways targeted by the drug, which lead to similar results compensating the downstream consequences of gender-specific differences in gene expression.


2006 ◽  
Vol 37 (2) ◽  
pp. 301-316 ◽  
Author(s):  
Andreas Petri ◽  
Jonas Ahnfelt-Rønne ◽  
Klaus Stensgaard Frederiksen ◽  
David George Edwards ◽  
Dennis Madsen ◽  
...  

To understand the molecular mechanisms regulating pancreatic endocrine development and function, pancreatic gene expression was compared between Ngn3-deficient mice and littermate controls on embryonic days 13 and 15. Microarray analysis identified 504 genes with significant differences in expression. Fifty-two of these showed at least twofold reduction in Ngn3 knockouts compared to controls. Many of them were previously described to be involved in endocrine development and function. Among the genes not previously characterized were Rhomboid veinlet-like 4, genes involved in tetrahydrobiopterin biosynthesis and the Iroquois-type homeobox gene Irx1, the latter was selected for further investigation. In situ hybridisation demonstrated that two Iroquois genes, Irx1 and Irx2, were expressed in pancreatic endoderm of wild-type, but not Ngn3 mutant embryos. Furthermore, ectopic Ngn3 induced prominent Irx2 expression in chicken endoderm. Co-labelling established that Irx1 and Irx2 mRNA is located to glucagon-, but not insulin- or somatostatin-producing cells in mice and chicken. These data suggest that Irx1 and Irx2 serve an evolutionary conserved role in the regulation of α-cell-specific gene expression.


2009 ◽  
Vol 46 (2) ◽  
pp. 257-270 ◽  
Author(s):  
Felix. D. Guerrero ◽  
Scot. E. Dowd ◽  
Yan Sun ◽  
Leonel Saldivar ◽  
Graham B. Wiley ◽  
...  

2003 ◽  
Vol 29 (2) ◽  
pp. 373-384 ◽  
Author(s):  
Marquis P Vawter ◽  
Simon Evans ◽  
Prabhakara Choudary ◽  
Hiroaki Tomita ◽  
Jim Meador-Woodruff ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document