C. Randak

发表

Cyclosporin A suppresses the expression of the interleukin 2 gene by inhibiting the binding of lymphocyte‐specific factors to the IL‐2 enhancer.

E. Serfling, T. Brabletz, C. Randak, 1990, The EMBO journal.

Protein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain.

L. D. Howell, J. Cohn, R. Borchardt, 2004, The Biochemical journal.

Monocyte derived macrophages from CF pigs exhibit increased inflammatory responses at birth

R. Gray, D. Stoltz, P. McCray, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Expression and functional properties of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator fused to glutathione-S-transferase.

E. Auerswald, I. Assfalg-Machleidt, W. Machleidt, 1995, FEBS letters.

An Intrinsic Adenylate Kinase Activity Regulates Gating of the ABC Transporter CFTR

M. Welsh, C. Randak, 2003, Cell.

Curcumin Stimulates Cystic Fibrosis Transmembrane Conductance Regulator Cl– Channel Activity*

M. Welsh, L. Ostedgaard, Philip H. Karp, 2005, Journal of Biological Chemistry.

Activation of G551D CFTR channel with MPB-91: regulation by ATPase activity and phosphorylation.

L. D. Howell, R. Dérand, J. Cohn, 2001, American journal of physiology. Cell physiology.

Three siblings with nonketotic hyperglycinaemia, mildly elevated plasma homocysteine concentrations and moderate methylmalonic aciduria

A. Roscher, D. Applegarth, B. Rolinski, 2000, Journal of Inherited Metabolic Disease.

Mutating the Conserved Q-loop Glutamine 1291 Selectively Disrupts Adenylate Kinase-dependent Channel Gating of the ATP-binding Cassette (ABC) Adenylate Kinase Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Reduces Channel Function in Primary Human Airway Epithelia*

M. Welsh, L. Ostedgaard, Viral S. Shah, 2015, The Journal of Biological Chemistry.

Airway acidification initiates host defense abnormalities in cystic fibrosis mice

David K. Meyerholz, Joseph Zabner, David A. Stoltz, 2016, Science.

Increased CFTR expression and function from an optimized lentiviral vector for cystic fibrosis gene therapy

S. Rivella, P. Sinn, P. McCray, 2021, Molecular therapy. Methods & clinical development.

CFTR with a partially deleted R domain corrects the cystic fibrosis chloride transport defect in human airway epithelia in vitro and in mouse nasal mucosa in vivo

M. Welsh, J. Zabner, A. Stecenko, 2002, Proceedings of the National Academy of Sciences of the United States of America.

CFTR-deficient pigs display peripheral nervous system defects at birth

M. Welsh, T. Moninger, D. Stoltz, 2013, Proceedings of the National Academy of Sciences.

Pretransplant management and small bowel-liver transplantation in an infant with microvillus inclusion disease.

J. Vanderhoof, A. Langnas, A. Phillips, 1998, Journal of pediatric gastroenterology and nutrition.

Processing and function of CFTR-ΔF508 are species-dependent

M. Welsh, L. Ostedgaard, C. Rogers, 2007, Proceedings of the National Academy of Sciences.

Processing and function of CFTR-DeltaF508 are species-dependent.

M. Welsh, L. Ostedgaard, C. Rogers, 2007, Proceedings of the National Academy of Sciences of the United States of America.

Adenylate Kinase Activity in ABC Transporters*

M. Welsh, C. Randak, 2005, Journal of Biological Chemistry.

ATP and AMP Mutually Influence Their Interaction with the ATP-binding Cassette (ABC) Adenylate Kinase Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) at Separate Binding Sites*

A. Elcock, M. Welsh, Qian Dong, 2013, The Journal of Biological Chemistry.

Demonstration of Phosphoryl Group Transfer Indicates That the ATP-binding Cassette (ABC) Transporter Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Exhibits Adenylate Kinase Activity*

M. Welsh, C. Randak, Amanda R. Ver Heul, 2012, The Journal of Biological Chemistry.

A mutation in CFTR modifies the effects of the adenylate kinase inhibitor Ap5A on channel gating.

M. Welsh, Qian Dong, C. Randak, 2008, Biophysical journal.

Role of CFTR’s intrinsic adenylate kinase activity in gating of the Cl− channel

M. Welsh, C. Randak, 2007, Journal of bioenergetics and biomembranes.

Expression and functional properties of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator fused to

E. Auerswald, I. Assfalg-Machleidt, W. Machleidt, 1995 .

ADP inhibits function of the ABC transporter cystic fibrosis transmembrane conductance regulator via its adenylate kinase activity.

M. Welsh, C. Randak, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia

M. Welsh, L. Ostedgaard, Philip H. Karp, 2003, Proceedings of the National Academy of Sciences of the United States of America.

A recombinant polypeptide model of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator is a GTP‐binding protein

E. Auerswald, P. Neth, W. Machleidt, 1996, FEBS letters.

A recombinant polypeptide model of the second nucleotide‐binding fold of the cystic fibrosis transmembrane conductance regulator functions as an active ATPase, GTPase and adenylate kinase

E. Auerswald, C. Eckerskorn, P. Neth, 1997, FEBS letters.

Inhibition of ATPase, GTPase and adenylate kinase activities of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator by genistein

E. Auerswald, W. Machleidt, W. Reenstra, 1999 .

Inhibition of ATPase, GTPase and adenylate kinase activities of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator by genistein.

E. Auerswald, W. Machleidt, W. Reenstra, 1999, The Biochemical journal.