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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 1
1993 1
2003 1
2004 2
2006 3
2007 3
2008 4
2009 2
2010 1
2012 14
2013 12
2014 10
2015 8
2016 7
2017 5
2018 13
2019 10
2020 6
2021 9
2022 9
2023 7
2024 0

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109 results

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Page 1
Chronic Granulomatous Disease: a Comprehensive Review.
Yu HH, Yang YH, Chiang BL. Yu HH, et al. Clin Rev Allergy Immunol. 2021 Oct;61(2):101-113. doi: 10.1007/s12016-020-08800-x. Clin Rev Allergy Immunol. 2021. PMID: 32524254 Review.
Chronic granulomatous disease (CGD) is a primary immunodeficiency of phagocyte function due to defective NADPH oxidase (phox). Compared with the common types of CYBB/gp91(phox), NCF1/p47(phox), and CYBA/p22(phox) deficiency, NCF4/p40(phox) deficiency is a mild and a …
Chronic granulomatous disease (CGD) is a primary immunodeficiency of phagocyte function due to defective NADPH oxidase (phox). Compared with …
Chronic Granulomatous Disease.
Leiding JW, Holland SM. Leiding JW, et al. 2012 Aug 9 [updated 2022 Apr 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2012 Aug 9 [updated 2022 Apr 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 22876374 Free Books & Documents. Review.
DIAGNOSIS/TESTING: The diagnosis of CGD is established in a proband with suggestive findings by identification of pathogenic variant(s) in one of six genes that encode or permit assembly of the subunits of phagocyte NADPH oxidase: biallelic pathogenic variants in CYBA, CYBC1, …
DIAGNOSIS/TESTING: The diagnosis of CGD is established in a proband with suggestive findings by identification of pathogenic variant(s) in o …
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients.
Cardamone G, Paraboschi EM, Soldà G, Duga S, Saarela J, Asselta R. Cardamone G, et al. Biomedicines. 2018 Dec 18;6(4):117. doi: 10.3390/biomedicines6040117. Biomedicines. 2018. PMID: 30567305 Free PMC article.
In this work, we screened for association with MS 11 single nucleotide polymorphisms (SNPs) and two microsatellite markers in the five genes (NCF1, NCF2, NCF4, CYBA, and CYBB) of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (NOX2) system, the enzy …
In this work, we screened for association with MS 11 single nucleotide polymorphisms (SNPs) and two microsatellite markers in the five genes …
Chronic Granulomatous Disease.
Roos D. Roos D. Methods Mol Biol. 2019;1982:531-542. doi: 10.1007/978-1-4939-9424-3_32. Methods Mol Biol. 2019. PMID: 31172494 Review.
Ncf1 polymorphism reveals oxidative regulation of autoimmune chronic inflammation.
Holmdahl R, Sareila O, Olsson LM, Bäckdahl L, Wing K. Holmdahl R, et al. Immunol Rev. 2016 Jan;269(1):228-47. doi: 10.1111/imr.12378. Immunol Rev. 2016. PMID: 26683156 Review.
The current review on the function of neutrophil cytosolic factor 1 (NCF1) and induced reactive oxygen species (ROS) is based on a genetic search for the major genes controlling autoimmune inflammatory disorders. ...Once cloned, it opened the possibility to dissect this co …
The current review on the function of neutrophil cytosolic factor 1 (NCF1) and induced reactive oxygen species (ROS) is based on a ge …
Chronic Granulomatous Disease.
Rawat A, Bhattad S, Singh S. Rawat A, et al. Indian J Pediatr. 2016 Apr;83(4):345-53. doi: 10.1007/s12098-016-2040-3. Epub 2016 Feb 11. Indian J Pediatr. 2016. PMID: 26865172 Review.
Recent topics and advanced therapies in chronic granulomatous disease.
Nunoi H, Nakamura H, Nishimura T, Matsukura M. Nunoi H, et al. Hum Cell. 2023 Mar;36(2):515-527. doi: 10.1007/s13577-022-00846-7. Epub 2022 Dec 19. Hum Cell. 2023. PMID: 36534309 Review.
Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by the inability of phagocytes to produce reactive oxygen species (ROS) owing to a defect in any of the five components (CYBB/gp91phox, CYBA/p22phox, NCF1/p47phox, NCF2/p67phox, and NCF4 …
Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by the inability of phagocytes to produce reactive oxygen sp …
Different unequal cross-over events between NCF1 and its pseudogenes in autosomal p47(phox)-deficient chronic granulomatous disease.
Hayrapetyan A, Dencher PC, van Leeuwen K, de Boer M, Roos D. Hayrapetyan A, et al. Biochim Biophys Acta. 2013 Oct;1832(10):1662-72. doi: 10.1016/j.bbadis.2013.05.001. Epub 2013 May 18. Biochim Biophys Acta. 2013. PMID: 23688784 Free article.
In 24 families the patients totally lacked NCF1 sequences, indicating that in these families the cross-over points are located between NCF1 and its pseudogenes. Six other families were compound heterozygous for a total NCF1 deletion and another mutation in …
In 24 families the patients totally lacked NCF1 sequences, indicating that in these families the cross-over points are located betwee …
Macrophages target Listeria monocytogenes by two discrete non-canonical autophagy pathways.
Gluschko A, Farid A, Herb M, Grumme D, Krönke M, Schramm M. Gluschko A, et al. Autophagy. 2022 May;18(5):1090-1107. doi: 10.1080/15548627.2021.1969765. Epub 2021 Sep 5. Autophagy. 2022. PMID: 34482812 Free PMC article.
This pore-forming toxin-induced non-canonical autophagy pathway (PINCA) was the only autophagic pathway evoked in tissue macrophages deficient for the NADPH oxidase CYBB/NOX2 that produces the reactive oxygen species (ROS) that are required for LAP induction. Similarly, al …
This pore-forming toxin-induced non-canonical autophagy pathway (PINCA) was the only autophagic pathway evoked in tissue macrophages deficie …
The phagocyte respiratory burst: Historical perspectives and recent advances.
Thomas DC. Thomas DC. Immunol Lett. 2017 Dec;192:88-96. doi: 10.1016/j.imlet.2017.08.016. Epub 2017 Aug 31. Immunol Lett. 2017. PMID: 28864335 Review.
This phagocyte respiratory burst is generated by an NADPH oxidase multi-protein complex that has a catalytic core consisting of membrane-bound gp91phox (CYBB) and p22phox (CYBA) sub-units and cytosolic components p47phox (NCF1), p67phox (NCF2) and p40phox (NCF4). .. …
This phagocyte respiratory burst is generated by an NADPH oxidase multi-protein complex that has a catalytic core consisting of membrane-bou …
109 results