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Science (New York, N.Y.)
|
July 7, 2000
Carbon nanotube-based nonvolatile random access memory for molecular computing
Rueckes, Kim, Joselevich, et al.
Nanotechnology
|
January 27, 2018
NRAM: a disruptive carbon-nanotube resistance-change memory
D C Gilmer, T Rueckes, L Cleveland
BMC Pulmonary Medicine
|
October 5, 2014
Intestinal current measurement versus nasal potential difference measurements for diagnosis of cystic fibrosis: a case-control study
Azadeh Bagheri-Hanson, Sebastian Nedwed, Claudia Rueckes-Nilges, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 11, 2014
Nasal potential difference: Best or average result for CFTR function as diagnostic criteria for cystic fibrosis?
Katherine Keenan, Julie Avolio, Claudia Rueckes-Nilges, et al.
Therapeutic Advances in Chronic Disease
|
August 12, 2022
Personalized medicine with drugs targeting the underlying protein defect in cystic fibrosis: is monitoring of treatment response necessary?
Katharina Niedermayr, Verena Gasser, Claudia Rueckes-Nilges, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 13, 2018
Effects of Lumacaftor-Ivacaftor Therapy on Cystic Fibrosis Transmembrane Conductance Regulator Function in Phe508del Homozygous Patients with Cystic Fibrosis
Simon Y Graeber, Christian Dopfer, Lutz Naehrlich, et al.
American Journal of Respiratory and Critical Care Medicine
|
December 22, 2021
Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two <i>F508del</i> Alleles
Simon Y Graeber, Constanze Vitzthum, Sophia T Pallenberg, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Science (New York, N.Y.)
|
July 7, 2000
Carbon nanotube-based nonvolatile random access memory for molecular computing
Rueckes, Kim, Joselevich, et al.
Nanotechnology
|
January 27, 2018
NRAM: a disruptive carbon-nanotube resistance-change memory
D C Gilmer, T Rueckes, L Cleveland
BMC Pulmonary Medicine
|
October 5, 2014
Intestinal current measurement versus nasal potential difference measurements for diagnosis of cystic fibrosis: a case-control study
Azadeh Bagheri-Hanson, Sebastian Nedwed, Claudia Rueckes-Nilges, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 11, 2014
Nasal potential difference: Best or average result for CFTR function as diagnostic criteria for cystic fibrosis?
Katherine Keenan, Julie Avolio, Claudia Rueckes-Nilges, et al.
Therapeutic Advances in Chronic Disease
|
August 12, 2022
Personalized medicine with drugs targeting the underlying protein defect in cystic fibrosis: is monitoring of treatment response necessary?
Katharina Niedermayr, Verena Gasser, Claudia Rueckes-Nilges, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 13, 2018
Effects of Lumacaftor-Ivacaftor Therapy on Cystic Fibrosis Transmembrane Conductance Regulator Function in Phe508del Homozygous Patients with Cystic Fibrosis
Simon Y Graeber, Christian Dopfer, Lutz Naehrlich, et al.
American Journal of Respiratory and Critical Care Medicine
|
December 22, 2021
Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two <i>F508del</i> Alleles
Simon Y Graeber, Constanze Vitzthum, Sophia T Pallenberg, et al.
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