scholarly journals Diagnosis of Gastrointestinal Cancer: Current Status and Recent Progress

1972 ◽  
Vol 63 (4) ◽  
pp. 672-700 ◽  
Author(s):  
Paul Sherlock ◽  
Alvin N. Ehrlich ◽  
Sidney J. Winawer
1967 ◽  
Vol 53 (4) ◽  
pp. 630-658 ◽  
Author(s):  
Paul Sherlock ◽  
Alvin N. Ehrlich ◽  
Eduardo E. Pavon ◽  
Michael A. Paglia

2021 ◽  
Author(s):  
Sourav Ghosh ◽  
Arindam Modak ◽  
Arnab Samanta ◽  
Kanika Kole ◽  
Subhra Jana

A comprehensive and critical in-depth discussion on the development and prospect of several advanced materials for conversion of CO2 to value added chemicals is provided, together with their current status, technical feasibility and future opportunities.


2017 ◽  
Vol 70 (2) ◽  
pp. 151-158 ◽  
Author(s):  
Nadia Boroumand ◽  
Hossein Saghi ◽  
Amir Avan ◽  
Amirhossein Bahreyni ◽  
Mikhail Ryzhikov ◽  
...  

2017 ◽  
Vol 232 (10) ◽  
pp. 2657-2673 ◽  
Author(s):  
Afsane Bahrami ◽  
Soodabeh Shahidsales ◽  
Majid Khazaei ◽  
Majid Ghayour-Mobarhan ◽  
Mina Maftouh ◽  
...  

Pathogens ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 405 ◽  
Author(s):  
Hany M. Elsheikha ◽  
Ruqaiyyah Siddiqui ◽  
Naveed Ahmed Khan

Although major strides have been made in developing and testing various anti-acanthamoebic drugs, recurrent infections, inadequate treatment outcomes, health complications, and side effects associated with the use of currently available drugs necessitate the development of more effective and safe therapeutic regimens. For any new anti-acanthamoebic drugs to be more effective, they must have either superior potency and safety or at least comparable potency and an improved safety profile compared to the existing drugs. The development of the so-called ‘next-generation’ anti-acanthamoebic agents to address this challenge is an active area of research. Here, we review the current status of anti-acanthamoebic drugs and discuss recent progress in identifying novel pharmacological targets and new approaches, such as drug repurposing, development of small interfering RNA (siRNA)-based therapies and testing natural products and their derivatives. Some of the discussed approaches have the potential to change the therapeutic landscape of Acanthamoeba infections.


2013 ◽  
Vol 110 (09) ◽  
pp. 450-457 ◽  
Author(s):  
Christos K. Kontos ◽  
Konstantinos Mavridis ◽  
Maroulio Talieri ◽  
Andreas Scorilas

SummaryThe human tissue kallikrein (KLK1) and kallikrein-related peptidases (KLKs) are secreted serine proteases with diverse expression patterns and physiological roles in different systems, including the digestive system. The aberrant expression of KLKs in gastrointestinal malignancies as well as their implication in carcinogenesis including cell growth regulation, angiogenesis, invasion, and metastasis, has prompted scientists to investigate their potential as cancer biomarkers. Expression of distinct KLKs is associated with various clinic-pathological parameters of patients with gastric, colorectal, pancreatic, hepatic, and esophageal cancer. Moreover, several KLKs possess significant favourable or unfavourable prognostic value in these human malignancies. Identification of novel diagnostic, prognostic and predictive biomarkers will contribute utmost to clinical decision-making, since early diagnosis of gastrointestinal cancer and early detection of recurrence following surgery are critical for the effective treatment of patients and for a positive clinical outcome. The current review provides a brief overview of the functional role of KLKs in gastric, colorectal, pancreatic, hepatic, and esophageal cancer, and describes the current status of KLKs as potential tumour biomarkers in these human malignancies.


2007 ◽  
Vol 85 (5) ◽  
pp. 531-540 ◽  
Author(s):  
U D Jentschura ◽  
M Haas

We report on recent progress in the treatment of two-loop binding corrections to the Lamb shift, with a special emphasis on S and P states. We use these and other results to infer an updated theoretical value of the Lamb shift in 4He+.PACS Nos.: 12.20.Ds, 31.30.Jv, 06.20.Jr, 31.15.–p


Sign in / Sign up

Export Citation Format

Share Document