نتایج جستجو برای: key deletion

تعداد نتایج: 628265  

Journal: :Cell 2002
Ruslan Aphasizhev Sandro Sbicego Marian Peris Sei-Heon Jang Inna Aphasizheva Agda M. Simpson Anatoly Rivlin Larry Simpson

A 3' terminal RNA uridylyltransferase was purified from mitochondria of Leishmania tarentolae and the gene cloned and expressed from this species and from Trypanosoma brucei. The enzyme is specific for 3' U-addition in the presence of Mg(2+). TUTase is present in vivo in at least two stable configurations: one contains a approximately 500 kDa TUTase oligomer and the other a approximately 700 kD...

2015
Martina Kluth Ramin Ahrary Claudia Hube-Magg Malik Ahmed Heinke Volta Catina Schwemin Stefan Steurer Corinna Wittmer Waldemar Wilczak Eike Burandt Till Krech Meike Adam Uwe Michl Hans Heinzer Georg Salomon Markus Graefen Christina Koop Sarah Minner Ronald Simon Guido Sauter Thorsten Schlomm

Deletion of 12p is a recurrent alteration in prostate cancer, but the prevalence and clinical consequences of this alteration have not been studied in detail. Dual labeling fluorescence in situ hybridization using probes for 12p13 (CDKN1B; p27) and centromere 12 as a reference was used to successfully analyze more than 3700 prostate cancers with clinical follow-up data assembled in a tissue mic...

Journal: :Journal of medical genetics 2004
M A Aldred R O C Sanford N S Thomas M A Barrow L C Wilson L A Brueton M C Bonaglia R C M Hennekam C Eng N R Dennis R C Trembath

T erminal deletions of the long arm of chromosome 2 (2q37) have been recorded in the literature for more than a decade and an associated syndrome first became apparent when nine patients were reported with an Albright hereditary osteodystrophy (AHO)-like metacarpal/ metatarsal shortening (brachymetaphalangism). 2 This is also known as brachydactyly-mental retardation syndrome (BDMR, MIM 600430)...

Journal: :IEICE Transactions on Fundamentals of Electronics, Communications and Computer Sciences 2022

We propose two systematic constructions of deletion-correcting codes for protecting quantum inforomation. The first one works with qudits any dimension ?, which is referred to as ?-adic, but only deletion corrected and the constructed are asymptotically bad. second corrects multiple deletions can construct good codes. also allows conversion stabilizer-based codes, entanglement assistance.

2016
Shiqiao Ye Toshifumi Fujiwara Jian Zhou Kottayil I Varughese Haibo Zhao

We have previously reported that depletion of LIS1, a key regulator of microtubules and cytoplasmic dynein motor complex, in osteoclast precursor cells by shRNAs attenuates osteoclastogenesis in vitro. However, the underlying mechanisms remain unclear. In this study, we show that conditional deletion of LIS1 in osteoclast progenitors in mice led to increased bone mass and decreased osteoclast n...

2018
Maximilian J. Surger Angel Angelov Philipp Stier Maria Übelacker Wolfgang Liebl

Micrococcus luteus naturally produces alkenes, unsaturated aliphatic hydrocarbons, and represents a promising host to produce hydrocarbons as constituents of biofuels and lubricants. In this work, we identify the genes for key enzymes of the branched-chain amino acid catabolism in M. luteus, whose first metabolic steps lead also to the formation of primer molecules for branched-chain fatty acid...

2011
Wei Wei Zhiyong Yang Chi-Hui Tang Limin Liu

S-nitrosoglutathione reductase (GSNOR), a ubiquitously expressed protein central to the control of protein S-nitrosylation, plays critical roles in many biological systems. We showed recently that GSNOR is often deficient in human hepatocellular carcinoma and that germ line deletion of the GSNOR gene in mice causes hepatocellular carcinoma through S-nitrosylation and proteasomal degradation of ...

Journal: :CoRR 2011
Yashodhan Kanoria Andrea Montanari

The deletion channel is the simplest point-to-point communication channel that models lack of synchronization. Input bits are deleted independently with probability d, and when they are not deleted, they are not affected by the channel. Despite significant effort, little is known about the capacity of this channel, and even less about optimal coding schemes. In this paper we develop a new syste...

2016
Kelly A. Rogers Sarah E. Moreno Laurie A. Smith Hervé Husson Nikolay O. Bukanov Steven R. Ledbetter Yeva Budman Yuefeng Lu Bing Wang Oxana Ibraghimov‐Beskrovnaya Thomas A. Natoli

Development of a disease-modifying therapy to treat autosomal dominant polycystic kidney disease (ADPKD) requires well-characterized preclinical models that accurately reflect the pathology and biochemical changes associated with the disease. Using a Pkd1 conditional knockout mouse, we demonstrate that subtly altering the timing and extent of Pkd1 deletion can have a significant impact on the o...

Journal: :Circulation 1994
K Nakai C Itoh Y Miura K Hotta T Musha T Itoh T Miyakawa R Iwasaki K Hiramori

BACKGROUND The angiotensin I-converting enzyme (ACE) is a key component of the renin-angiotensin system thought to be important in the pathogenesis of hypertension and cardiovascular disease. Deletion polymorphism in the ACE gene may be a risk factor for myocardial infarction in the Caucasian population. However, this finding has not yet been investigated in the Japanese population. METHODS A...

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