نتایج جستجو برای: de novo programming

تعداد نتایج: 1852646  

1999
Vadim Kapustkin

The study investigates the innovation, investment and international trade performance of the russian firms, based on the questionnaire survey data. The data were collected from 150 enterprises of the st. Petersburg area (northwest russia). Half of the firms represented in the survey are de novo and another half consists of stateowned and privatized firms. The study’s hypothesis is that the firm...

2002
Helen Pomykala

A major unresolved question for the 11q23 translocations involving MLL is the chromosomal mechanism(s1 leading to these translocations. We have mapped breakpoints within the 8.3-kb BamHl breakpoint cluster region in 31 patients with acute lymphoblastic leukemia and acute myeloid leukemia (AML) de novo and in 8 t-AML patients. In 23 of 31 leukemia de novo patients, MLL breakpoints mapped to the ...

Journal: :Journal of proteome research 2012
Swapnil Bhatia Yong J Kil Beatrix Ueberheide Brian T Chait Lemmuel Tayo Lourdes Cruz Bingwen Lu John R Yates Marshall Bern

De novo peptide sequencing by mass spectrometry (MS) can determine the amino acid sequence of an unknown peptide without reference to a protein database. MS-based de novo sequencing assumes special importance in focused studies of families of biologically active peptides and proteins, such as hormones, toxins, and antibodies, for which amino acid sequences may be difficult to obtain through gen...

2014
Heming Wang Xiaofeng Zhu

De novo mutations enrich the sequence diversity and carry the clue of evolutional selection. Recent studies suggest the de novo mutations could be one of the risk factors for complex diseases. We conducted a survey of de novo mutations using the whole genome sequence data but only available on the odd autosomes of Mexican American families provided by Genetic Analysis Workshop 18. We extracted ...

Journal: :American journal of human genetics 2016
William M Brandler Danny Antaki Madhusudan Gujral Amina Noor Gabriel Rosanio Timothy R Chapman Daniel J Barrera Guan Ning Lin Dheeraj Malhotra Amanda C Watts Lawrence C Wong Jasper A Estabillo Therese E Gadomski Oanh Hong Karin V Fuentes Fajardo Abhishek Bhandari Renius Owen Michael Baughn Jeffrey Yuan Terry Solomon Alexandra G Moyzis Michelle S Maile Stephan J Sanders Gail E Reiner Keith K Vaux Charles M Strom Kang Zhang Alysson R Muotri Natacha Akshoomoff Suzanne M Leal Karen Pierce Eric Courchesne Lilia M Iakoucheva Christina Corsello Jonathan Sebat

Genetic studies of autism spectrum disorder (ASD) have established that de novo duplications and deletions contribute to risk. However, ascertainment of structural variants (SVs) has been restricted by the coarse resolution of current approaches. By applying a custom pipeline for SV discovery, genotyping, and de novo assembly to genome sequencing of 235 subjects (71 affected individuals, 26 hea...

Journal: :Neuron 2011
Dheeraj Malhotra Shane McCarthy Jacob J. Michaelson Vladimir Vacic Katherine E. Burdick Seungtai Yoon Sven Cichon Aiden Corvin Sydney Gary Elliot S. Gershon Michael Gill Maria Karayiorgou John R. Kelsoe Olga Krastoshevsky Verena Krause Ellen Leibenluft Deborah L. Levy Vladimir Makarov Abhishek Bhandari Anil K. Malhotra Francis J. McMahon Markus M. Nöthen James B. Potash Marcella Rietschel Thomas G. Schulze Jonathan Sebat

While it is known that rare copy-number variants (CNVs) contribute to risk for some neuropsychiatric disorders, the role of CNVs in bipolar disorder is unclear. Here, we reasoned that a contribution of CNVs to mood disorders might be most evident for de novo mutations. We performed a genome-wide analysis of de novo CNVs in a cohort of 788 trios. Diagnoses of offspring included bipolar disorder ...

2017
Ignacio Vázquez-García Francisco Salinas Jing Li Andrej Fischer Benjamin Barré Johan Hallin Anders Bergström Elisa Alonso-Perez Jonas Warringer Ville Mustonen Gianni Liti

The joint contribution of pre-existing and de novo genetic variation to clonal adaptation is poorly understood but essential to designing successful antimicrobial or cancer therapies. To address this, we evolve genetically diverse populations of budding yeast, S. cerevisiae, consisting of diploid cells with unique haplotype combinations. We study the asexual evolution of these populations under...

Journal: :Infection and immunity 2017
Carrie L Shaffer Ellisa W Zhang Anne G Dudley Beverly R E A Dixon Kirsten R Guckes Erin J Breland Kyle A Floyd Daniel P Casella Holly M Scott Algood Douglass B Clayton Maria Hadjifrangiskou

The ability to de novo synthesize purines has been associated with the intracellular survival of multiple bacterial pathogens. Uropathogenic Escherichia coli (UPEC), the predominant cause of urinary tract infections, undergoes a transient intracellular lifestyle during which bacteria clonally expand into multicellular bacterial communities within the cytoplasm of bladder epithelial cells. Here,...

Journal: :Current Biology 2001
Wallace F Marshall Yvonne Vucica Joel L Rosenbaum

BACKGROUND Centriole duplication is a key step in the cell cycle whose mechanism is completely unknown. Why new centrioles always form next to preexisting ones is a fundamental question. The simplest model is that preexisting centrioles nucleate the assembly of new centrioles, and that although centrioles can in some cases form de novo without this nucleation, the de novo assembly mechanism sho...

2016
Yu-Mu Chen Ying-Tang Fang Chien-Hao Lai Kun-Ming Rau Cheng-Hua Huang Huang-Chih Chang Tung-Ying Chao Chia-Cheng Tseng Wen-Feng Fang Chin-Chou Wang Yung-Che Chen Yu-Hsiu Chung Yi-Hsi Wang Mao-Chang Su Shih-Feng Liu Kuo-Tung Huang Hung-Chen Chen Ya-Chun Chang Yu-Ping Chang Meng-Chih Lin

In the pre-tyrosine kinase inhibitors (TKIs) era, non-small cell lung cancer (NSCLC) patients with de novo bone metastases had a worse prognosis than those without. However, whether epidermal growth factor receptor (EGFR)-TKIs affect the outcomes of EGFR mutant NSCLC patients with de novo bone metastases has not been well studied thus far. We retrospectively studied the effect of EGFR mutation ...

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