Search Results - "Carson, Johnny L"

Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype by Davis, Stephanie D, Ferkol, Thomas W, Rosenfeld, Margaret, Lee, Hye-Seung, Dell, Sharon D, Sagel, Scott D, Milla, Carlos, Zariwala, Maimoona A, Pittman, Jessica E, Shapiro, Adam J, Carson, Johnny L, Krischer, Jeffrey P, Hazucha, Milan J, Cooper, Matthew L, Knowles, Michael R, Leigh, Margaret W

“…The relationship between clinical phenotype of childhood primary ciliary dyskinesia (PCD) and ultrastructural defects and genotype is poorly defined. To…”
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Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents by Leigh, Margaret W, Ferkol, Thomas W, Davis, Stephanie D, Lee, Hye-Seung, Rosenfeld, Margaret, Dell, Sharon D, Sagel, Scott D, Milla, Carlos, Olivier, Kenneth N, Sullivan, Kelli M, Zariwala, Maimoona A, Pittman, Jessica E, Shapiro, Adam J, Carson, Johnny L, Krischer, Jeffrey, Hazucha, Milan J, Knowles, Michael R

“…Primary ciliary dyskinesia (PCD), a genetically heterogeneous, recessive disorder of motile cilia, is associated with distinct clinical features. Diagnostic…”
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Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia by Leigh, Margaret W, Hazucha, Milan J, Chawla, Kunal K, Baker, Brock R, Shapiro, Adam J, Brown, David E, Lavange, Lisa M, Horton, Bethany J, Qaqish, Bahjat, Carson, Johnny L, Davis, Stephanie D, Dell, Sharon D, Ferkol, Thomas W, Atkinson, Jeffrey J, Olivier, Kenneth N, Sagel, Scott D, Rosenfeld, Margaret, Milla, Carlos, Lee, Hye-Seung, Krischer, Jeffrey, Zariwala, Maimoona A, Knowles, Michael R

“…Several studies suggest that nasal nitric oxide (nNO) measurement could be a test for primary ciliary dyskinesia (PCD), but the procedure and interpretation…”
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Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome by Leigh, Margaret W, Pittman, Jessica E, Carson, Johnny L, Ferkol, Thomas W, Dell, Sharon D, Davis, Stephanie D, Knowles, Michael R, Zariwala, Maimoona A

“…Primary ciliary dyskinesia is a genetically heterogeneous disorder of motile cilia. Most of the disease-causing mutations identified to date involve the heavy…”
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Exome Sequencing Identifies Mutations in CCDC114 as a Cause of Primary Ciliary Dyskinesia by Knowles, Michael R., Leigh, Margaret W., Ostrowski, Lawrence E., Huang, Lu, Carson, Johnny L., Hazucha, Milan J., Yin, Weining, Berg, Jonathan S., Davis, Stephanie D., Dell, Sharon D., Ferkol, Thomas W., Rosenfeld, Margaret, Sagel, Scott D., Milla, Carlos E., Olivier, Kenneth N., Turner, Emily H., Lewis, Alexandra P., Bamshad, Michael J., Nickerson, Deborah A., Shendure, Jay, Zariwala, Maimoona A.

“…Primary ciliary dyskinesia (PCD) is a genetically heterogeneous, autosomal-recessive disorder, characterized by oto-sino-pulmonary disease and situs…”
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Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms by Knowles, Michael R., Ostrowski, Lawrence E., Loges, Niki T., Hurd, Toby, Leigh, Margaret W., Huang, Lu, Wolf, Whitney E., Carson, Johnny L., Hazucha, Milan J., Yin, Weining, Davis, Stephanie D., Dell, Sharon D., Ferkol, Thomas W., Sagel, Scott D., Olivier, Kenneth N., Jahnke, Charlotte, Olbrich, Heike, Werner, Claudius, Raidt, Johanna, Wallmeier, Julia, Pennekamp, Petra, Dougherty, Gerard W., Hjeij, Rim, Gee, Heon Yung, Otto, Edgar A., Halbritter, Jan, Chaki, Moumita, Diaz, Katrina A., Braun, Daniela A., Porath, Jonathan D., Schueler, Markus, Baktai, György, Griese, Matthias, Turner, Emily H., Lewis, Alexandra P., Bamshad, Michael J., Nickerson, Deborah A., Hildebrandt, Friedhelm, Shendure, Jay, Omran, Heymut, Zariwala, Maimoona A.

“…Primary ciliary dyskinesia (PCD) is a genetically heterogeneous, autosomal-recessive disorder, characterized by oto-sino-pulmonary disease and situs…”
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Culturing of human nasal epithelial cells at the air liquid interface by Müller, Loretta, Brighton, Luisa E, Carson, Johnny L, Fischer, 2nd, William A, Jaspers, Ilona

“…In vitro models using human primary epithelial cells are essential in understanding key functions of the respiratory epithelium in the context of microbial…”
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Claudin-18: a dominant tight junction protein in Barrett's esophagus and likely contributor to its acid resistance by Jovov, Biljana, Van Itallie, Christina M, Shaheen, Nicholas J, Carson, Johnny L, Gambling, Todd M, Anderson, James M, Orlando, Roy C

“…Barrett's esophagus (BE) is a specialized columnar epithelium (SCE) that develops as replacement for damaged squamous epithelium (SqE) in subjects with reflux…”
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Role of claudin interactions in airway tight junctional permeability by Coyne, Carolyn B, Gambling, Todd M, Boucher, Richard C, Carson, Johnny L, Johnson, Larry G

“…Airway epithelial tight junctions (TJs) serve to separate the external and internal environments of the lung. However, the members of the claudin family that…”
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The Gillings Sampler – An electrostatic air sampler as an alternative method for aerosol in vitro exposure studies by Zavala, Jose, Lichtveld, Kim, Ebersviller, Seth, Carson, Johnny L., Walters, Glenn W., Jaspers, Ilona, Jeffries, Harvey E., Sexton, Kenneth G., Vizuete, William

“…•We developed an electrostatic air sampler to expose cells at the air–liquid interface.•We developed a reproducible positive aerosol control method for cell…”
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Regulation of airway tight junctions by proinflammatory cytokines by Coyne, Carolyn B, Vanhook, Miriam K, Gambling, Todd M, Carson, Johnny L, Boucher, Richard C, Johnson, Larry G

“…Epithelial tight junctions (TJs) provide an important route for passive electrolyte transport across airway epithelium and provide a barrier to the migration…”
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Air Pollution and Brain Damage by Calderón-Garcidueñas, Lilian, Azzarelli, Biagio, Acuna, Hilda, Garcia, Raquel, Gambling, Todd M., Osnaya, Norma, Monroy, Sylvia, Del Rosario Tizapantzi, Maria, Carson, Johnny L., Villarreal-Calderon, Anna, Rewcastle, Barry

“…Exposure to complex mixtures of air pollutants produces infl ammation in the upper and lower respiratory tract. Because the nasal cavity is a common portal of…”
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Bacterial Penetration of Bladder Epithelium through Lipid Rafts by Duncan, Matthew J, Li, Guojie, Shin, Jeoung-Sook, Carson, Johnny L, Abraham, Soman N

“…Type 1 fimbriated Escherichia coli represents the most common human uropathogen, owing much of its virulence to invasion of the uroepithelium, which is highly…”
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Cinnamaldehyde in flavored e-cigarette liquids temporarily suppresses bronchial epithelial cell ciliary motility by dysregulation of mitochondrial function by Clapp, Phillip W, Lavrich, Katelyn S, van Heusden, Catharina A, Lazarowski, Eduardo R, Carson, Johnny L, Jaspers, Ilona

“…Aldehydes in cigarette smoke (CS) impair mitochondrial function and reduce ciliary beat frequency (CBF), leading to diminished mucociliary clearance (MCC)…”
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Laterality Defects Other Than Situs Inversus Totalis in Primary Ciliary Dyskinesia by Shapiro, Adam J, MD, Davis, Stephanie D, MD, Ferkol, Thomas, MD, Dell, Sharon D, MD, Rosenfeld, Margaret, MD, Olivier, Kenneth N, MD, Sagel, Scott D, MD, Milla, Carlos, MD, Zariwala, Maimoona A, PhD, Wolf, Whitney, BS, Carson, Johnny L, PhD, Hazucha, Milan J, MD, PhD, Burns, Kimberlie, Robinson, Blair, MD, Knowles, Michael R, MD, Leigh, Margaret W, MD

“…BACKGROUND Motile cilia dysfunction causes primary ciliary dyskinesia (PCD), situs inversus totalis (SI), and a spectrum of laterality defects, yet the…”
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Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy by Shapiro, Adam J, Davis, Stephanie D, Ferkol, Thomas, Dell, Sharon D, Rosenfeld, Margaret, Olivier, Kenneth N, Sagel, Scott D, Milla, Carlos, Zariwala, Maimoona A, Wolf, Whitney, Carson, Johnny L, Hazucha, Milan J, Burns, Kimberlie, Robinson, Blair, Knowles, Michael R, Leigh, Margaret W

“…Motile cilia dysfunction causes primary ciliary dyskinesia (PCD), situs inversus totalis (SI), and a spectrum of laterality defects, yet the prevalence of…”
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Epithelial Cells from Smokers Modify Dendritic Cell Responses in the Context of Influenza Infection by Horvath, Katherine M., Brighton, Luisa E., Zhang, Wenli, Carson, Johnny L., Jaspers, Ilona

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DYX1C1 is required for axonemal dynein assembly and ciliary motility by Tarkar, Aarti, Loges, Niki T, Slagle, Christopher E, Francis, Richard, Dougherty, Gerard W, Tamayo, Joel V, Shook, Brett, Cantino, Marie, Schwartz, Daniel, Jahnke, Charlotte, Olbrich, Heike, Werner, Claudius, Raidt, Johanna, Pennekamp, Petra, Abouhamed, Marouan, Hjeij, Rim, Köhler, Gabriele, Griese, Matthias, Li, You, Lemke, Kristi, Klena, Nikolas, Liu, Xiaoqin, Gabriel, George, Tobita, Kimimasa, Jaspers, Martine, Morgan, Lucy C, Shapiro, Adam J, Letteboer, Stef J F, Mans, Dorus A, Carson, Johnny L, Leigh, Margaret W, Wolf, Whitney E, Chen, Serafine, Lucas, Jane S, Onoufriadis, Alexandros, Plagnol, Vincent, Schmidts, Miriam, Boldt, Karsten, Roepman, Ronald, Zariwala, Maimoona A, Lo, Cecilia W, Mitchison, Hannah M, Knowles, Michael R, Burdine, Rebecca D, LoTurco, Joseph J, Omran, Heymut

“…Heymut Omran, Joseph LoTurco and colleagues show that mutations in the dyslexia susceptibility candidate gene DYX1C1 cause primary ciliary dyskinesia. Their…”
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Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype by KNOWLES, Michael R, OSTROWSKI, Lawrence E, ROSENFELD, Margaret, FERKOL, Thomas W, DELL, Sharon D, MILLA, Carlos E, RANDELL, Scott H, WEINING YIN, SANNUTI, Aruna, METJIAN, Hilda M, NOONE, Peadar G, NOONE, Peter J, LEIGH, Margaret W, OLSON, Christina A, PATRONE, Michael V, HONG DANG, LEE, Hye-Seung, HURD, Toby W, HEON YUNG GEE, OTTO, Edgar A, HALBRITTER, Jan, KOHL, Stefan, KIRCHER, Martin, SEARS, Patrick R, KRISCHER, Jeffrey, BAMSHAD, Michael J, NICKERSON, Deborah A, HILDEBRANDT, Friedhelm, SHENDURE, Jay, ZARIWALA, Maimoona A, DAVIS, Stephanie D, WOLF, Whitney E, HAZUCHA, Milan J, CARSON, Johnny L, OLIVIER, Kenneth N, SAGEL, Scott D

“…Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia, but the genetic cause is not defined for all patients with…”
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Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure by Knowles, Michael R, Leigh, Margaret W, Carson, Johnny L, Davis, Stephanie D, Dell, Sharon D, Ferkol, Thomas W, Olivier, Kenneth N, Sagel, Scott D, Rosenfeld, Margaret, Burns, Kimberlie A, Minnix, Susan L, Armstrong, Michael C, Lori, Adriana, Hazucha, Milan J, Loges, Niki T, Olbrich, Heike, Becker-Heck, Anita, Schmidts, Miriam, Werner, Claudius, Omran, Heymut, Zariwala, Maimoona A

“…Primary ciliary dyskinesia (PCD) is an autosomal recessive, genetically heterogeneous disorder characterised by oto-sino-pulmonary disease and situs…”
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