Search Results - "Cant, Natasha"

Detergent-free purification of ABC (ATP-binding-cassette) transporters by Gulati, Sonali, Jamshad, Mohammed, Knowles, Timothy J, Morrison, Kerrie A, Downing, Rebecca, Cant, Natasha, Collins, Richard, Koenderink, Jan B, Ford, Robert C, Overduin, Michael, Kerr, Ian D, Dafforn, Timothy R, Rothnie, Alice J

“…ABC (ATP-binding-cassette) transporters carry out many vital functions and are involved in numerous diseases, but study of the structure and function of these…”
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Detection of phospho-sites generated by protein kinase CK2 in CFTR: mechanistic aspects of Thr1471 phosphorylation by Venerando, Andrea, Franchin, Cinzia, Cant, Natasha, Cozza, Giorgio, Pagano, Mario A, Tosoni, Kendra, Al-Zahrani, Ateeq, Arrigoni, Giorgio, Ford, Robert C, Mehta, Anil, Pinna, Lorenzo A

“…By mass spectrometry analysis of mouse Cystic Fibrosis Transmembrane-conductance Regulator (mCFTR) expressed in yeast we have detected 21 phosphopeptides…”
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Systematic evaluation of PAXgene® tissue fixation for the histopathological and molecular study of lung cancer by Southwood, Mark, Krenz, Tomasz, Cant, Natasha, Maurya, Manisha, Gazdova, Jana, Maxwell, Perry, McGready, Claire, Moseley, Ellen, Hughes, Susan, Stewart, Peter, Salto‐Tellez, Manuel, Groelz, Daniel, Rassl, Doris

“…Whilst adequate for most existing pathological tests, formalin is generally considered a poor DNA preservative and use of alternative fixatives may prove…”
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Structure of the cystic fibrosis transmembrane conductance regulator in the inward-facing conformation revealed by single particle electron microscopy by Al-Zahrani, Ateeq, Cant, Natasha, Kargas, Vassilis, Rimington, Tracy, Aleksandrov, Luba, R. Riordan, John, C. Ford, Robert

“…The most common inherited disease in European populations is cystic fibrosis. Mutations in the gene lead to loss of function of the cystic fibrosis…”
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CFTR structure and cystic fibrosis by Cant, Natasha, Pollock, Naomi, Ford, Robert C.

“…CFTR (cystic fibrosis transmembrane conductance regulator) is a member of the ATP-binding cassette family of membrane proteins. Although almost all members of…”
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Abstract 2745: Evaluation of a new system for collection, stabilization, and purification of circulating tumor DNA by Fleischhacker, Michael, Schmidt, Bernd, Baker, Rohan, Pedersen, Susanne, Cant, Natasha, Zahedi-Nejad, Maryam, Voss, Thorsten, Ullius, Andrea, Groelz, Daniel

“…Abstract Introduction: The current preanalytical workflows for circulating tumor DNA (ctDNA) analysis have limitations that affect the accurate detection and…”
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Purification of the cystic fibrosis transmembrane conductance regulator protein expressed in Saccharomyces cerevisiae by Pollock, Naomi, Cant, Natasha, Rimington, Tracy, Ford, Robert C

“…Defects in the cystic fibrosis transmembrane conductance regulator (CFTR) protein cause cystic fibrosis (CF), an autosomal recessive disease that currently…”
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A survey of detergents for the purification of stable, active human cystic fibrosis transmembrane conductance regulator (CFTR) by Hildebrandt, Ellen, Zhang, Qinghai, Cant, Natasha, Ding, Haitao, Dai, Qun, Peng, Lingling, Fu, Yu, DeLucas, Lawrence J., Ford, Robert, Kappes, John C., Urbatsch, Ina L.

“…Structural knowledge of the cystic fibrosis transmembrane conductance regulator (CFTR) requires developing methods to purify and stabilize this…”
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Purification of the Cystic Fibrosis Transmembrane Conductance Regulator Protein Expressed in Saccharomyces cerevisiae by Pollock, Naomi, Cant, Natasha, Rimington, Tracy, Ford, Robert C.

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Expression and Purification of the Cystic Fibrosis Transmembrane Conductance Regulator From Saccharomyces cerevisiae for High-Resolution Structural Studies by Cant, Natasha

“…The cystic fibrosis transmembrane conductance regulator (CFTR) is an ABC transporter family protein that acts as an ion channel. Mutations in CFTR cause the…”
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Expression and purification of the cystic fibrosis transmembrane conductance regulator protein in Saccharomyces cerevisiae by O'Ryan, Liam, Rimington, Tracy, Cant, Natasha, Ford, Robert C

“…The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel, that when mutated, can give rise to cystic fibrosis in humans.There is…”
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Expression and Purification of the Cystic Fibrosis Transmembrane Conductance Regulator Protein in Saccharomyces cerevisiae by O'Ryan, Liam, Rimington, Tracy, Cant, Natasha, Ford, Robert C.

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