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Items: 1 to 20 of 21

1.
Three cdg Operons Control Cellular Turnover of Cyclic Di-GMP in Acetobacter xylinum: Genetic Organization and Occurrence of Conserved Domains in Isoenzymes
Rony Tal, Hing C. Wong, Roger Calhoon, David Gelfand, Anna Lisa Fear, Gail Volman, Raphael Mayer, Peter Ross, Dorit Amikam, Haim Weinhouse, Avital Cohen, Shai Sapir, Patricia Ohana, Moshe Benziman
J Bacteriol. 1998 Sep; 180(17): 4416–4425. doi: 10.1128/jb.180.17.4416-4425.1998
PMCID:
PMC107450
AbstractArticlePDF–481K
2.
Characterization of Dense Granule Metalloproteinase INS-16 in Cryptosporidium parvum
Hao Cui, Rui Xu, Yu Li, Yaqiong Guo, Ziding Zhang, Lihua Xiao, Yaoyu Feng, Na Li
Int J Mol Sci. 2022 Jul; 23(14): 7617. Published online 2022 Jul 10. doi: 10.3390/ijms23147617
PMCID:
PMC9315855
AbstractArticlePDF–2.4M
3.
Fluorogenic Probes with Substitutions at the 2 and 7 Positions of Cephalosporin are Highly BlaC-Specific for Rapid Mycobacterium tuberculosis Detection
Yunfeng Cheng, Hexin Xie, Preeti Sule, Hany Hassounah, Edward A Graviss, Ying Kong, Jeffrey D Cirillo, Jianghong Rao
Angew Chem Int Ed Engl. 2014 Aug 25; 53(35): 9360–9364. Published online 2014 Jul 2. doi: 10.1002/anie.201405243
PMCID:
PMC4499257
AbstractArticlePDF–1019K
4.
Characterization of INS-15, A Metalloprotease Potentially Involved in the Invasion of Cryptosporidium parvum
Rui Xu, Yaqiong Guo, Na Li, Qiang Zhang, Haizhen Wu, Una Ryan, Yaoyu Feng, Lihua Xiao
Microorganisms. 2019 Oct; 7(10): 452. Published online 2019 Oct 14. doi: 10.3390/microorganisms7100452
PMCID:
PMC6843835
AbstractArticlePDF–1.8M
5.
Rapid Tuberculosis Diagnosis Using Reporter Enzyme Fluorescence
Preeti Sule, Ronak Tilvawala, Toriq Mustapha, Hany Hassounah, Aneesa Noormohamed, Suprateek Kundu, Edward A. Graviss, Grant K. Walkup, Ying Kong, Jeffrey D. Cirillo
J Clin Microbiol. 2019 Dec; 57(12): e01462-19. Prepublished online 2019 Sep 11. Published online 2019 Nov 22. doi: 10.1128/JCM.01462-19
PMCID:
PMC6879286
AbstractArticlePDF–3.7M
6.
Discovery of New Microneme Proteins in Cryptosporidium parvum and Implication of the Roles of a Rhomboid Membrane Protein (CpROM1) in Host–Parasite Interaction
Xin Gao, Jigang Yin, Dongqiang Wang, Xiaohui Li, Ying Zhang, Chenchen Wang, Yuanyuan Zhang, Guan Zhu
Front Vet Sci. 2021; 8: 778560. Published online 2021 Dec 13. doi: 10.3389/fvets.2021.778560
PMCID:
PMC8710574
AbstractArticlePDF–10M
7.
Comparative Characterization of CpCDPK1 and CpCDPK9, Two Potential Drug Targets against Cryptosporidiosis
Jiayuan Su, Yiting Shen, Na Li, Yu Li, Ziding Zhang, Lihua Xiao, Yaqiong Guo, Yaoyu Feng
Microorganisms. 2022 Feb; 10(2): 333. Published online 2022 Feb 1. doi: 10.3390/microorganisms10020333
PMCID:
PMC8875172
AbstractArticlePDF–2.2M
8.
Stabilization of Tuberculosis Reporter Enzyme Fluorescence (REFtb) Diagnostic Reagents for Use at the Point of Care
Maxim Lebedev, Aaron B. Benjamin, Kent J. Koster, Kathryn E. Broyles, Sathish Kumar, Joseph M. Jilka, Jeffrey D. Cirillo
Diagnostics (Basel) 2022 Jul; 12(7): 1745. Published online 2022 Jul 19. doi: 10.3390/diagnostics12071745
PMCID:
PMC9324015
AbstractArticlePDF–6.3M
9.
Hematopoietic Cell Transplantation for Chronic Granulomatous Disease in Japan
Masakatsu Yanagimachi, Koji Kato, Akihiro Iguchi, Koji Sasaki, Chikako Kiyotani, Katsuyoshi Koh, Takashi Koike, Hideki Sano, Tomonari Shigemura, Hideki Muramatsu, Keiko Okada, Masami Inoue, Ken Tabuchi, Toyoki Nishimura, Tomoyuki Mizukami, Hiroyuki Nunoi, Kohsuke Imai, Masao Kobayashi, Tomohiro Morio
Front Immunol. 2020; 11: 1617. Published online 2020 Jul 29. doi: 10.3389/fimmu.2020.01617
PMCID:
PMC7403177
AbstractArticlePDF–562K
10.
Clinical and genetic characteristics of Chinese pediatric patients with chronic granulomatous disease
Li‐Wei Gao, Qing‐Qin Yin, Yue‐Juan Tong, Jin‐Gang Gui, Xiu‐yun Liu, Xue‐li Feng, Ju Yin, Jun Liu, Yan Guo, Yao Yao, Bao‐Ping Xu, Jian‐Xin He, Kun‐Ling Shen, Yu‐Lung Lau, Zai‐Fang Jiang
Pediatr Allergy Immunol. 2019 May; 30(3): 378–386. Published online 2019 Mar 27. doi: 10.1111/pai.13033
PMCID:
PMC6850071
AbstractArticlePDF–421K
11.
Bleeding Assessment in female patients with the Hermansky-Pudlak syndrome - A Case Series
DR. Joel Rivera-Concepción, Jorge Acevedo-Canabal, Antonio Burés, Gustavo Vargas, Carmen Cadilla, Natalio J. Izquierdo
Eur J Haematol. Author manuscript; available in PMC 2020 May 1.
Published in final edited form as: Eur J Haematol. 2019 May; 102(5): 432–436. Published online 2019 Mar 6. doi: 10.1111/ejh.13210
PMCID:
PMC6545108
ArticlePDF–68K
12.
NCF1 (p47phox)–deficient chronic granulomatous disease: comprehensive genetic and flow cytometric analysis
Douglas B. Kuhns, Amy P. Hsu, David Sun, Karen Lau, Danielle Fink, Paul Griffith, Da Wei Huang, Debra A. Long Priel, Laura Mendez, Samantha Kreuzburg, Christa S. Zerbe, Suk See De Ravin, Harry L. Malech, Steven M. Holland, Xiaolin Wu, John I. Gallin
Blood Adv. 2019 Jan 22; 3(2): 136–147. Published online 2019 Jan 16. doi: 10.1182/bloodadvances.2018023184
PMCID:
PMC6341190
AbstractArticlePDF–1.4M
13.
Inherited p40phox deficiency differs from classic chronic granulomatous disease
Annemarie van de Geer, Alejandro Nieto-Patlán, Douglas B. Kuhns, Anton T.J. Tool, Andrés A. Arias, Matthieu Bouaziz, Martin de Boer, José Luis Franco, Roel P. Gazendam, John L. van Hamme, Michel van Houdt, Karin van Leeuwen, Paul J.H. Verkuijlen, Timo K. van den Berg, Juan F. Alzate, Carlos A. Arango-Franco, Vritika Batura, Andrea R. Bernasconi, Barbara Boardman, Claire Booth, Siobhan O. Burns, Felipe Cabarcas, Nadine Cerf Bensussan, Fabienne Charbit-Henrion, Anniek Corveleyn, Caroline Deswarte, María Esnaola Azcoiti, Dirk Foell, John I. Gallin, Carlos Garcés, Margarida Guedes, Claas H. Hinze, Steven M. Holland, Stephen M. Hughes, Patricio Ibañez, Harry L. Malech, Isabelle Meyts, Marcela Moncada-Velez, Kunihiko Moriya, Esmeralda Neves, Matias Oleastro, Laura Perez, Vimel Rattina, Carmen Oleaga-Quintas, Neil Warner, Aleixo M. Muise, Jeanet Serafín López, Eunice Trindade, Julia Vasconcelos, Séverine Vermeire, Helmut Wittkowski, Austen Worth, Laurent Abel, Mary C. Dinauer, Peter D. Arkwright, Dirk Roos, Jean-Laurent Casanova, Taco W. Kuijpers, Jacinta Bustamante
J Clin Invest. 2018 Aug 31; 128(9): 3957–3975. Published online 2018 Aug 6. doi: 10.1172/JCI97116
PMCID:
PMC6118590
AbstractArticlePDF–7.6M
14.
Chronic Granulomatous Disease: A Large, Single-center US Experience
Pietro Bortoletto, Kyle Lyman, Andres Camacho, Marielle Fricchione, Aaruni Khanolkar, Ben Z. Katz
Pediatr Infect Dis J. 2015 Oct; 34(10): 1110–1114. Published online 2015 Sep 15. doi: 10.1097/INF.0000000000000840
PMCID:
PMC4568897
AbstractArticlePDF–332K
15.
Genetic disorders coupled to ROS deficiency
Sharon O’Neill, Julie Brault, Marie-Jose Stasia, Ulla G. Knaus
Redox Biol. 2015 Dec; 6: 135–156. Published online 2015 Jul 17. doi: 10.1016/j.redox.2015.07.009
PMCID:
PMC4550764
AbstractArticlePDF–4.4M
16.
Assessment of Atherosclerosis in Chronic Granulomatous Disease
Christopher T. Sibley, Tyra Estwick, Anna Zavodni, Chiung-Yu Huang, Alan C. Kwan, Benjamin P. Soule, Debra A. Long Priel, Alan T. Remaley, Amanda K. Rudman Spergel, Evrim B. Turkbey, Douglas B. Kuhns, Steven M. Holland, Harry L. Malech, Kol A. Zarember, David A. Bluemke, John I. Gallin
Circulation. Author manuscript; available in PMC 2015 Dec 2.
Published in final edited form as: Circulation. 2014 Dec 2; 130(23): 2031–2039. Published online 2014 Sep 19. doi: 10.1161/CIRCULATIONAHA.113.006824
PMCID:
PMC4258873
AbstractArticlePDF–492K
17.
NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2
Aleixo M Muise, Wei Xu, Cong-Hui Guo, Thomas D Walters, Victorien M Wolters, Ramzi Fattouh, Grace Y Lam, Pingzhao Hu, Ryan Murchie, Mary Sherlock, Juan Cristóbal Gana, NEOPICS, Richard K Russell, Michael Glogauer, Richard H Duerr, Judy H Cho, Charlie W Lees, Jack Satsangi, David C Wilson, Andrew D Paterson, Anne M Griffiths, Mark S Silverberg, John H Brumell
Gut. Author manuscript; available in PMC 2013 Oct 23.
Published in final edited form as: Gut. 2012 Jul; 61(7): 1028–1035. Published online 2011 Sep 7. doi: 10.1136/gutjnl-2011-300078
Correction in:
Gut, volume 62 on page 1432
PMCID:
PMC3806486
AbstractArticlePDF–635K
18.
A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40phox and selective defects in neutrophil NADPH oxidase activity
Juan D. Matute, Andres A. Arias, Nicola A. M. Wright, Iwona Wrobel, Christopher C. M. Waterhouse, Xing Jun Li, Christophe C. Marchal, Natalie D. Stull, David B. Lewis, MacGregor Steele, James D. Kellner, Weiming Yu, Samy O. Meroueh, William M. Nauseef, Mary C. Dinauer
Blood. 2009 Oct 8; 114(15): 3309–3315. Prepublished online 2009 Aug 19. doi: 10.1182/blood-2009-07-231498
PMCID:
PMC2759653
AbstractArticle
19.
Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1).
U Francke, C L Hsieh, B E Foellmer, K J Lomax, H L Malech, T L Leto
Am J Hum Genet. 1990 Sep; 47(3): 483–492.
PMCID:
PMC1683885
SummaryPage BrowsePDF–2.1M
20.
Cytosolic components of the respiratory burst oxidase: resolution of four components, two of which are missing in complementing types of chronic granulomatous disease.
J T Curnutte, P J Scott, L A Mayo
Proc Natl Acad Sci U S A. 1989 Feb; 86(3): 825–829. doi: 10.1073/pnas.86.3.825
PMCID:
PMC286570
SummaryPage BrowsePDF–1.1M

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