نتایج جستجو برای: برنامة nbn

تعداد نتایج: 1711  

Journal: :Telecommunications Journal of Australia 2013

2014
Goutham Hassan Venkatesh Vadhiraja Bejadi Manjunath Kamalesh Dattaram Mumbrekar Hitendra Negi Donald Jerard Fernandes Krishna Sharan Sourjya Banerjee Satish Rao Bola Sadashiva

Cellular and molecular approaches are being explored to find a biomarker which can predict the development of radiation induced acute toxicity prior to radiation therapy. SNPs in radiation responsive genes may be considered as an approach to develop tools for finding the inherited basis of clinical radiosensitivity. The current study attempts to screen single nucleotide polymorphisms/deletions ...

Journal: :Experimental neurology 2008
Yaniv Assaf Ronit Galron Itai Shapira Anat Nitzan Tamar Blumenfeld-Katzir Arieh S Solomon Vered Holdengreber Zhao-Qi Wang Yosef Shiloh Ari Barzilai

Nijmegen breakage syndrome (NBS) is a genomic instability disease caused by hypomorphic mutations in the NBS1 gene encoding the Nbs1 (nibrin) protein. Nbs1 is a component of the Mre11/Rad50/Nbs1 (MRN) complex that acts as a sensor of double strand breaks (DSBs) in the DNA and is critical for proper activation of the broad cellular response to DSBs. Conditional disruption of the murine ortholog ...

Journal: :Cancer research 2009
Mariana C Stern Jie Lin Jonine D Figueroa Karl T Kelsey Anne E Kiltie Jian-Min Yuan Giuseppe Matullo Tony Fletcher Simone Benhamou Jack A Taylor Donatella Placidi Zuo-Feng Zhang Gunnar Steineck Nathaniel Rothman Manolis Kogevinas Debra Silverman Nuria Malats Stephen Chanock Xifeng Wu Margaret R Karagas Angeline S Andrew Heather H Nelson D Timothy Bishop Sei Chung Sak Ananya Choudhury Jennifer H Barrett Faye Elliot Román Corral Amit D Joshi Manuela Gago-Dominguez Victoria K Cortessis Yong-Bing Xiang Yu-Tang Gao Paolo Vineis Carlotta Sacerdote Simonetta Guarrera Silvia Polidoro Alessandra Allione Eugen Gurzau Kvetoslava Koppova Rajiv Kumar Peter Rudnai Stefano Porru Angela Carta Marcello Campagna Cecilia Arici Sung Shim Lani Park Montserrat Garcia-Closas

Tobacco smoking is the most important and well-established bladder cancer risk factor and a rich source of chemical carcinogens and reactive oxygen species that can induce damage to DNA in urothelial cells. Therefore, common variation in DNA repair genes might modify bladder cancer risk. In this study, we present results from meta-analyses and pooled analyses conducted as part of the Internatio...

2012
Harald Krenzlin Ilja Demuth Bastian Salewsky Petra Wessendorf Kathrin Weidele Alexander Bürkle Martin Digweed

Nijmegen Breakage Syndrome (NBS), an autosomal recessive genetic instability syndrome, is caused by hypomorphic mutation of the NBN gene, which codes for the protein nibrin. Nibrin is an integral member of the MRE11/RAD50/NBN (MRN) complex essential for processing DNA double-strand breaks. Cardinal features of NBS are immunodeficiency and an extremely high incidence of hematological malignancie...

2003

186 LLE Review, Volume 92 Recently proposed superconducting single-photon detectors (SSPD’s), based on ultrathin, submicrometer-width NbN superconducting stripes, are characterized by picosecond response times, high quantum efficiency, broadband singlephoton sensitivity, and extremely low dark counts.1,2 The devices have immediately found a variety of applications ranging from noninvasive testi...

2017
Pham Vu Nhat Devashis Majumdar Jerzy Leszczynski Minh Tho Nguyen

A comprehensive review on geometric and electronic structures, spectroscopic and energetic properties of small niobium clusters in the range from two to twenty atoms, Nbn, n = 2–20, in three different charged states is presented including a systematic comparison of quantum chemical results with available experimental data to assign the lowest-lying structures of Nbn clusters and their IR spectr...

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