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39 publications found

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Group #1

Matched potential author: Philip H Karp - author of 5 items
TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Amphotericin B induces epithelial voltage responses in people with cystic fibrosis[1]Rajeev S Chorghade, [2]Bo Ram Kim, [3]Janice L Launspach, [4]Philip H Karp, [5]Michael J Welsh, [6]Martin D Burke [Full author list]Journal of Cystic Fibrosis [missing]DOI: 10.1016/J.JCF.2020.11.018 [ORCID]
PubMed: 33309058 [ORCID]
cystic fibrosis [missing]; amphotericin B [missing]2020-12-08Philip H Karp (Q125262782; 5 items)
Heterogeneous expression of the SARS-Coronavirus-2 receptor ACE2 in the human respiratory tract[1]Miguel E Ortiz, [2]Andrew Thurman, [3]Alejandro A Pezzulo, [4]Mariah R Leidinger, [5]Julia A Klesney-Tait, [6]Philip H Karp, [7]Ping Tan, [8]Christine Wohlford-Lenane, [9]Paul B McCray, [10]David K Meyerholz [Full author list]EBioMedicine [missing]DOI: 10.1016/J.EBIOM.2020.102976 [ORCID]
PubMed: 32971472 [ORCID]
2020-09-21
TNFα and IL-17 Alkalinize Airway Surface Liquid through CFTR and Pendrin[1]Tayyab Rehman, [2]Ian M Thornell, [3]Alejandro A Pezzulo, [4]Andrew L Thurman, [5]Guillermo S Romano Ibarra, [6]Philip H Karp, [7]Ping Tan, [8]Michael E Duffey, [9]Michael J Welsh [Full author list]American Journal of Physiology - Cell Physiology [missing]DOI: 10.1152/AJPCELL.00112.2020 [ORCID]
PubMed: 32432926 [ORCID]
2020-05-20Philip H Karp (Q125262782; 5 items)
Heterogeneous expression of the SARS-Coronavirus-2 receptor ACE2 in the human respiratory tract[1]Miguel E Ortiz Bezara, [1-Q95611124]Miguel Ortiz Bezara, [10-Q42482570]David Meyerholz, [2]Andrew Thurman, [3]Alejandro A Pezzulo, [4]Mariah R Leidinger, [5]Julia A Klesney-Tait, [6]Philip H Karp, [7]Ping Tan, [8]Christine Wohlford-Lenane, [9]Paul B McCray, [10]David K Meyerholz, [3-Q57320737]Alejandro A Pezzulo, [5-Q61474893]Julia Klesney-Tait, [9-Q55189490]Paul B McCray [Full author list]DOI: 10.1101/2020.04.22.056127 [ORCID]
PubMed: 32577664 [ORCID]
2020-04-24Philip H Karp (Q125262782; 5 items)
Small-molecule ion channels increase host defences in cystic fibrosis airway epithelia[1]Katrina A Muraglia, [2]Rajeev S Chorghade, [3]Bo Ram Kim, [4]Xiao Xiao Tang, [5]Viral S Shah, [6]Anthony S Grillo, [7]Page N Daniels, [8]Alexander G Cioffi, [9]Philip H Karp, [10]Lingyang Zhu, [11]Michael J Welsh, [12]Martin D Burke [Full author list]Nature [missing]DOI: 10.1038/S41586-019-1018-5 [ORCID]
PubMed: 30867598 [ORCID]
cystic fibrosis [missing]2019-03-13Philip H Karp (Q125262782; 5 items)
Lack of cystic fibrosis transmembrane conductance regulator disrupts fetal airway development in pigs[1]David Meyerholz, [2]David Stoltz, [3]Nick D Gansemer, [4]Sarah E Ernst, [5]Daniel P Cook, [6]Matthew D Strub, [7]Erica N LeClair, [8]Carrie K Barker, [9]Ryan J Adam, [10]Mariah R Leidinger, [11]Katherine N Gibson-Corley, [12]Philip H Karp, [13]Michael J Welsh, [14]Paul B McCray [Full author list]Laboratory Investigation [missing]DOI: 10.1038/S41374-018-0026-7 [ORCID]
PubMed: 29467455 [ORCID]
cystic fibrosis [missing]; transmembrane protein [missing]2018-02-21Philip H Karp (Q125262782; 5 items)
Nominal carbonic anhydrase activity minimizes airway-surface liquid pH changes during breathing[1]Ian M Thornell, [2]Xiaopeng Li, [3]Xiao Xiao Tang, [4]Christian M Brommel, [5]Philip H Karp, [6]Michael J Welsh, [7]Joseph Zabner [Full author list]Physiological Reports [missing]DOI: 10.14814/PHY2.13569 [ORCID]
PubMed: 29380953 [ORCID]
breathing [missing]2018-01-01Philip H Karp (Q125262782; 5 items)
Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies[1]Viral S Shah, [2]Sarah Ernst, [3]Xiao Xiao Tang, [4]Philip H Karp, [5]Connor P Parker, [6]Lynda S Ostedgaard, [7]Michael J Welsh [Full author list]Proceedings of the National Academy of Sciences of the United States of America [missing]DOI: 10.1073/PNAS.1604905113 [ORCID]
PubMed: 27114540 [ORCID]
cystic fibrosis [missing]2016-04-25Philip H Karp (Q125262782; 5 items)
Acidic pH increases airway surface liquid viscosity in cystic fibrosis[1]Xiao Xiao Tang, [2]Lynda S Ostedgaard, [3]Mark J Hoegger, [4]Thomas O Moninger, [5]Philip H Karp, [6]James D McMenimen, [7]Biswa Choudhury, [8]Ajit Varki, [9]David Stoltz, [10]Michael J Welsh [Full author list]Journal of Clinical Investigation [missing]DOI: 10.1172/JCI83922 [ORCID]
PubMed: 26808501 [ORCID]
cystic fibrosis [missing]2016-01-25Philip H Karp (Q125262782; 5 items)
Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense[1]Xiaopeng Li, [2]Xiao Xiao Tang, [3]Luis G Vargas Buonfiglio, [4]Alejandro P. Comellas, [5]Ian M Thornell, [6]Shyam Ramachandran, [7]Philip H Karp, [8]Peter J Taft, [9]Kelsey Sheets, [10]Mahmoud H Abou Alaiwa, [11]Michael J Welsh, [12]David Meyerholz, [13]David Stoltz, [14]Joseph Zabner [Full author list]American Journal of Physiology - Lung Cellular and Molecular Physiology [missing]DOI: 10.1152/AJPLUNG.00422.2015 [ORCID]
PubMed: 26801568 [ORCID]
cystic fibrosis [missing]2016-01-22Philip H Karp (Q125262782; 5 items)
Airway acidification initiates host defense abnormalities in cystic fibrosis mice[1]Viral S Shah, [2]David Meyerholz, [3]Xiao Xiao Tang, [4]Leah R Reznikov, [5]Mahmoud H Abou Alaiwa, [6]Sarah E Ernst, [7]Philip H Karp, [8]Christine L Wohlford-Lenane, [9]Kristopher P Heilmann, [10]Mariah R Leidinger, [11]Patrick D Allen, [12]Joseph Zabner, [13]Paul B McCray, [14]Lynda S Ostedgaard, [15]David Stoltz, [16]Christoph O Randak, [17]Michael J Welsh [Full author list]Science [missing]DOI: 10.1126/SCIENCE.AAD5589 [ORCID]
PubMed: 26823428 [ORCID]
cystic fibrosis [missing]2016-01-01Philip H Karp (Q125262782; 5 items)
Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor[1]Eugene H Chang, [2]Xiao Xiao Tang, [3]Viral S Shah, [4]Janice L Launspach, [5]Sarah E Ernst, [6]Brieanna Hilkin, [7]Philip H Karp, [8]Mahmoud H Abou Alaiwa, [9]Scott M Graham, [10]Douglas B Hornick, [11]Michael J Welsh, [12]David Stoltz, [13]Joseph Zabner [Full author list]International forum of allergy & rhinology [missing]DOI: 10.1002/ALR.21440 [ORCID]
PubMed: 25363320 [ORCID]
cystic fibrosis [missing]2014-10-31Philip H Karp (Q125262782; 5 items)
A genomic signature approach to rescue ΔF508-cystic fibrosis transmembrane conductance regulator biosynthesis and function[1]Shyam Ramachandran, [2]Samantha R Osterhaus, [3]Philip H Karp, [4]Michael J Welsh, [5]Paul B McCray [Full author list]American Journal of Respiratory Cell and Molecular Biology [missing]DOI: 10.1165/RCMB.2014-0007OC [ORCID]
PubMed: 24669817 [ORCID]
cystic fibrosis [missing]2014-09-01Philip H Karp (Q125262782; 5 items)
Chemosensory functions for pulmonary neuroendocrine cells[1]Xiaoling Gu, [2]Philip H Karp, [3]Steven L Brody, [4]Richard A Pierce, [5]Michael J Welsh, [6]Michael J Holtzman, [7]Yehuda Ben-Shahar [Full author list]American Journal of Respiratory Cell and Molecular Biology [missing]DOI: 10.1165/RCMB.2013-0199OC [ORCID]
PubMed: 24134460 [ORCID]
chemosensation [missing]2014-03-01Philip H Karp (Q125262782; 5 items)
Post-transcriptional regulation of cystic fibrosis transmembrane conductance regulator expression and function by microRNAs[1]Shyam Ramachandran, [2]Philip H Karp, [3]Samantha R Osterhaus, [4]Peng Jiang, [5]Christine Wohlford-Lenane, [6]Kim A Lennox, [7]Ashley M Jacobi, [8]Kal Praekh, [9]Scott D Rose, [10]Mark A. Behlke, [11]Yi Xing, [12]Michael J Welsh, [13]Paul B McCray [Full author list]American Journal of Respiratory Cell and Molecular Biology [missing]DOI: 10.1165/RCMB.2012-0430OC [ORCID]
PubMed: 23646886 [ORCID]
cystic fibrosis [missing]; microRNA [missing]; transmembrane protein [missing]2013-10-01Philip H Karp (Q125262782; 5 items)
Multicenter intestinal current measurements in rectal biopsies from CF and non-CF subjects to monitor CFTR function[1]John P Clancy, [2]Rhonda D Szczesniak, [3]Melissa A Ashlock, [4]Sarah E Ernst, [5]Lijuan Fan, [6]Douglas B Hornick, [7]Philip H Karp, [8]Umer Khan, [9]James Lymp, [10]Alicia J Ostmann, [11]Amir Rezayat, [12]Timothy D Starner, [13]Shajan P Sugandha, [14]Hongtao Sun, [15]Nancy Quinney, [16]Scott H Donaldson, [17]Steven M Rowe, [18]Sherif E Gabriel [Full author list]PLOS One [missing]DOI: 10.1371/JOURNAL.PONE.0073905 [ORCID]
PubMed: 24040112 [ORCID]
multicenter clinical trial [missing]2013-09-10
Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs[1]David Stoltz, [2]Tatiana Rokhlina, [3]Sarah E Ernst, [4]Alejandro A Pezzulo, [5]Lynda S Ostedgaard, [6]Philip H Karp, [7]Melissa S Samuel, [8]Leah R Reznikov, [9]Michael V Rector, [10]Nicholas D Gansemer, ... [Full author list]Journal of Clinical Investigation [missing]DOI: 10.1172/JCI68867 [ORCID]
PubMed: 23676501 [ORCID]
cystic fibrosis [missing]; meconium [missing]; meconium ileus [missing]; intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency [missing]2013-05-08Philip H Karp (Q125262782; 5 items)
Adenoviral gene transfer corrects the ion transport defect in the sinus epithelia of a porcine CF model[1]Andrea E Potash, [2]Tanner J Wallen, [3]Philip H Karp, [4]Sarah Ernst, [5]Thomas O Moninger, [6]Nicholas D Gansemer, [7]David Stoltz, [8]Joseph Zabner, [9]Eugene H Chang [Full author list]Molecular Therapy [missing]DOI: 10.1038/MT.2013.49 [ORCID]
PubMed: 23511247 [ORCID]
Adenoviridae [missing]2013-03-19Philip H Karp (Q125262782; 5 items)
Integrin α6β4 identifies human distal lung epithelial progenitor cells with potential as a cell-based therapy for cystic fibrosis lung disease[1]Xiaopeng Li, [2]Nathan Rossen, [3]Patrick L. Sinn, [4]Andrew L Hornick, [5]Benjamin R Steines, [6]Philip H Karp, [7]Sarah E Ernst, [8]Ryan J Adam, [9]Thomas O Moninger, [10]Dana N Levasseur, [11]Joseph Zabner [Full author list]PLOS One [missing]DOI: 10.1371/JOURNAL.PONE.0083624 [ORCID]
PubMed: 24349537 [ORCID]
cystic fibrosis [missing]2013-01-01Philip H Karp (Q125262782; 5 items)
Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis[1]Eugene H Chang, [2]Alejandro A Pezzulo, [3]David Meyerholz, [4]Andrea E Potash, [5]Tanner J Wallen, [6]Leah R Reznikov, [7]Jessica C Sieren, [8]Philip H Karp, [9]Sarah Ernst, [10]Thomas O Moninger, [11]Nicholas D Gansemer, [12]Paul B McCray, [13]David Stoltz, [14]Michael J Welsh, [15]Joseph Zabner [Full author list]The Laryngoscope [missing]DOI: 10.1002/LARY.23392 [ORCID]
PubMed: 22711071 [ORCID]
cystic fibrosis [missing]2012-06-18Philip H Karp (Q125262782; 5 items)
CFTR is required for maximal transepithelial liquid transport in pig alveolar epithelia[1]Xiaopeng Li, [2]Alejandro P. Comellas, [3]Philip H Karp, [4]Sarah E Ernst, [5]Thomas O Moninger, [6]Nicholas D Gansemer, [7]Peter J Taft, [8]Alejandro A Pezzulo, [9]Michael V Rector, [10]Nathan Rossen, [11]David Stoltz, [12]Paul B McCray, [13]Michael J Welsh, [14]Joseph Zabner [Full author list]American Journal of Physiology - Lung Cellular and Molecular Physiology [missing]DOI: 10.1152/AJPLUNG.00116.2012 [ORCID]
PubMed: 22637155 [ORCID]
2012-05-25Philip H Karp (Q125262782; 5 items)
The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs[1]Lynda S Ostedgaard, [2]David Meyerholz, [3]Jeng-Haur Chen, [4]Alejandro A Pezzulo, [5]Philip H Karp, [6]Tatiana Rokhlina, [7]Sarah E Ernst, [8]Robert A Hanfland, [9]Leah R Reznikov, [10]Paula S Ludwig, ... [Full author list]Science Translational Medicine [missing]DOI: 10.1126/SCITRANSLMED.3001868 [ORCID]
PubMed: 21411740 [ORCID]
cystic fibrosis [missing]2011-03-01Philip H Karp (Q125262782; 5 items)
Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- mice[1]Lynda S Ostedgaard, [2]David Meyerholz, [3]Daniel W Vermeer, [4]Philip H Karp, [5]Lindsey Schneider, [6]Curt D. Sigmund, [7]Michael J Welsh [Full author list]Proceedings of the National Academy of Sciences of the United States of America [missing]DOI: 10.1073/PNAS.1019752108 [ORCID]
PubMed: 21285372 [ORCID]
phenotype [missing]; cystic fibrosis [missing]; transmembrane protein [missing]2011-02-01Philip H Karp (Q125262782; 5 items)
Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia[1]Jeng-Haur Chen, [2]David A Stoltz, [3]Philip H Karp, [4]Sarah E Ernst, [5]Alejandro A Pezzulo, [6]Thomas O Moninger, [7]Michael V Rector, [8]Leah R Reznikov, [9]Janice L Launspach, [10]Kathryn Chaloner, [11]Joseph Zabner, [12]Michael J Welsh [Full author list]Cell [missing]DOI: 10.1016/J.CELL.2010.11.029 [ORCID]
PubMed: 21145458 [ORCID]
cystic fibrosis [missing]2010-12-01Philip H Karp (Q125262782; 5 items)
Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth[1]David Stoltz, [2]David Meyerholz, [3]Alejandro A Pezzulo, [4]Shyam Ramachandran, [5]Mark P Rogan, [6]Greg J Davis, [7]Robert A Hanfland, [8]Chris Wohlford-Lenane, [9]Cassie L Dohrn, [10]Jennifer A Bartlett, ..., [18]Melissa Samuel, [19]Tatiana Rokhlina, [20]Philip H Karp, [21]Lynda S Ostedgaard, [22]Aliye Uc, ... [Full author list]Science Translational Medicine [missing]DOI: 10.1126/SCITRANSLMED.3000928 [ORCID]
PubMed: 20427821 [ORCID]
cystic fibrosis [missing]; eradication of infectious diseases [missing]2010-04-01Philip H Karp (Q125262782; 5 items)
Adenovirus 5-fiber 35 chimeric vector mediates efficient apical correction of the cystic fibrosis transmembrane conductance regulator defect in cystic fibrosis primary airway epithelia[1]Ophélia Granio, [2]Katherine J D Ashbourne Excoffon, [3]Petra Henning, [4]Patricia Melin, [5]Caroline Norez, [6]Gaëlle Gonzalez, [7]Philip H Karp, [8]Maria K Magnusson, [9]Nagy Habib, [10]Leif Lindholm, [11]Frédéric Becq, [12]Pierre Boulanger, [13]Joseph Zabner, [14]Saw-See Hong [Full author list]Human Gene Therapy [missing]DOI: 10.1089/HUM.2009.056 [ORCID]
PubMed: 19788389 [ORCID]
cystic fibrosis [missing]; Adenoviridae [missing]; transmembrane protein [missing]2010-03-01Philip H Karp (Q125262782; 5 items)
Isoform-specific regulation and localization of the coxsackie and adenovirus receptor in human airway epithelia[1]Katherine J D A Excoffon, [2]Nicholas D Gansemer, [3]Matthew E Mobily, [4]Philip H Karp, [5]Kalpaj R Parekh, [6]Joseph Zabner [Full author list]PLOS One [missing]DOI: 10.1371/JOURNAL.PONE.0009909 [ORCID]
PubMed: 20361046 [ORCID]
virology [missing]; Adenoviridae [missing]; CXADR Ig-like cell adhesion molecule [missing]2010-01-01Philip H Karp (Q125262782; 5 items)
MMP9 modulates tight junction integrity and cell viability in human airway epithelia[1]Paola D Vermeer, [2]James Denker, [3]Miriam Estin, [4]Thomas O Moninger, [5]Shaf Baloch Keshavjee, [6]Philip Karp, [7]Joel N Kline, [8]Joseph Zabner [Full author list]American Journal of Physiology - Lung Cellular and Molecular Physiology [missing]DOI: 10.1152/AJPLUNG.90578.2008 [ORCID]
PubMed: 19270179 [ORCID]
2009-03-06Philip H Karp (Q125262782; 5 items)
Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs[1]Christopher S Rogers, [2]David Stoltz, [3]David Meyerholz, [4]Lynda S Ostedgaard, [5]Tatiana Rokhlina, [6]Peter J Taft, [7]Mark P Rogan, [8]Alejandro A Pezzulo, [9]Philip H Karp, [10]Omar A Itani, [11]Amanda C Kabel, ... [Full author list]Science [missing]DOI: 10.1126/SCIENCE.1163600 [ORCID]
PubMed: 18818360 [ORCID]
cystic fibrosis [missing]2008-09-01Philip H Karp (Q125262782; 5 items)
Processing and function of CFTR-DeltaF508 are species-dependent[1]Lynda S Ostedgaard, [2]Christopher S Rogers, [3]Qian Dong, [4]Christoph O Randak, [5]Daniel W Vermeer, [6]Tatiana Rokhlina, [7]Philip H Karp, [8]Michael J Welsh [Full author list]Proceedings of the National Academy of Sciences of the United States of America [missing]DOI: 10.1073/PNAS.0706974104 [ORCID]
PubMed: 17873061 [ORCID]
2007-09-14Philip H Karp (Q125262782; 5 items)
Cellular localization and activity of Ad-delivered GFP-CFTR in airway epithelial and tracheal cells[1]Ophélia Granio, [2]Caroline Norez, [3]Katherine J D Ashbourne Excoffon, [4]Philip H Karp, [5]Monika Lusky, [6]Frédéric Becq, [7]Pierre Boulanger, [8]Joseph Zabner, [9]Saw-See Hong [Full author list]American Journal of Respiratory Cell and Molecular Biology [missing]DOI: 10.1165/RCMB.2007-0026TE [ORCID]
PubMed: 17641299 [ORCID]
2007-07-19Philip H Karp (Q125262782; 5 items)
Differentiation of human airway epithelia is dependent on erbB2[1]Paola D Vermeer, [2]Lacey Panko, [3]Philip Karp, [4]John H Lee, [5]Joseph Zabner [Full author list]American Journal of Physiology - Lung Cellular and Molecular Physiology [missing]DOI: 10.1152/AJPLUNG.00547.2005 [ORCID]
PubMed: 16489114 [ORCID]
2006-02-17Philip H Karp (Q125262782; 5 items)
Gene transfer of CFTR to airway epithelia: low levels of expression are sufficient to correct Cl- transport and overexpression can generate basolateral CFTR[1]Sara L Farmen, [2]Philip H Karp, [3]Philip Ng, [4]Donna J Palmer, [5]David R Koehler, [6]Jim Hu, [7]Arthur L Beaudet, [8]Joseph Zabner, [9]Michael J Welsh [Full author list]American Journal of Physiology - Lung Cellular and Molecular Physiology [missing]DOI: 10.1152/AJPLUNG.00049.2005 [ORCID]
PubMed: 16085675 [ORCID]
overexpression [missing]2005-08-05Philip H Karp (Q125262782; 5 items)
A shortened adeno-associated virus expression cassette for CFTR gene transfer to cystic fibrosis airway epithelia[1]Lynda S Ostedgaard, [2]Tatiana Rokhlina, [3]Philip H Karp, [4]Philip Lashmit, [5]Sandra Afione, [6]Michael Schmidt, [7]Joseph Zabner, [8]Mark F Stinski, [9]Jay A Chiorini, [10]Michael J Welsh [Full author list]Proceedings of the National Academy of Sciences of the United States of America [missing]DOI: 10.1073/PNAS.0409845102 [ORCID]
PubMed: 15703296 [ORCID]
cystic fibrosis [missing]2005-02-09Philip H Karp (Q125262782; 5 items)
Curcumin stimulates cystic fibrosis transmembrane conductance regulator Cl- channel activity[1]Allan L Berger, [2]Christoph O Randak, [3]Lynda S Ostedgaard, [4]Philip H Karp, [5]Daniel W Vermeer, [6]Michael J Welsh [Full author list]Journal of Biological Chemistry [missing]DOI: 10.1074/JBC.M412972200 [ORCID]
PubMed: 15582996 [ORCID]
cystic fibrosis [missing]; curcumin [missing]; transmembrane protein [missing]2004-12-06Philip H Karp (Q125262782; 5 items)
Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia[1]Lynda S Ostedgaard, [2]Christoph O Randak, [3]Tatiana Rokhlina, [4]Philip Karp, [5]Daniel Vermeer, [6]Katherine J Ashbourne Excoffon, [7]Michael J Welsh [Full author list]Proceedings of the National Academy of Sciences of the United States of America [missing]DOI: 10.1073/PNAS.2627982100 [ORCID]
PubMed: 12578973 [ORCID]
cystic fibrosis [missing]; transmembrane protein [missing]2003-02-10Philip H Karp (Q125262782; 5 items)
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[1]Lynda S Ostedgaard, [2]Joseph Zabner, [3]Daniel W Vermeer, [4]Tatiana Rokhlina, [5]Philip H Karp, [6]Arlene A Stecenko, [7]Christoph Randak, [8]Michael J Welsh [Full author list]Proceedings of the National Academy of Sciences of the United States of America [missing]DOI: 10.1073/PNAS.261714599 [ORCID]
PubMed: 11854474 [ORCID]
cystic fibrosis [missing]2002-02-19Philip H Karp (Q125262782; 5 items)
An in vitro model of differentiated human airway epithelia. Methods for establishing primary cultures.[1]Philip H Karp, [2]Thomas O Moninger, [3]S Pary Weber, [4]Tamara S Nesselhauf, [5]Janice L Launspach, [6]Joseph Zabner, [7]Michael J Welsh [Full author list]Methods in Molecular Biology [missing]DOI: 10.1385/1-59259-185-X:115 [ORCID]
PubMed: 11987537 [ORCID]
2002-01-01

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