Similar articles for PMID: 15367430

Year	Number of Results
1994	2
1996	1
1998	5
2000	1
2001	1
2002	2
2003	7
2004	1
2005	4
2006	5
2007	2
2008	7
2009	2
2010	2
2011	2
2012	4
2013	4
2014	4
2015	4
2016	3
2017	7
2018	6
2019	5
2020	3
2024	0

1

Deficiency of somatic hypermutation of the antibody light chain is associated with increased frequency of severe respiratory tract infection in common variable immunodeficiency.

Andersen P, Permin H, Andersen V, Schejbel L, Garred P, Svejgaard A, Barington T. Andersen P, et al. Blood. 2005 Jan 15;105(2):511-7. doi: 10.1182/blood-2003-12-4359. Epub 2004 Sep 14. Blood. 2005. PMID: 15367430 Free article.

2

Deficiency of somatic hypermutation of immunoglobulin G transcripts is a better predictor of severe respiratory tract infections than lack of memory B cells in common variable immunodeficiency.

Schejbel L, Marquart H, Andersen V, Permin H, Andersen P, Svejgaard A, Barington T. Schejbel L, et al. J Clin Immunol. 2005 Jul;25(4):392-403. doi: 10.1007/s10875-005-5034-x. J Clin Immunol. 2005. PMID: 16133996

3

Noninfectious complications in patients with pediatric-onset common variable immunodeficiency correlated with defects in somatic hypermutation but not in class-switch recombination.

Almejún MB, Campos BC, Patiño V, Galicchio M, Zelazko M, Oleastro M, Oppezzo P, Danielian S. Almejún MB, et al. J Allergy Clin Immunol. 2017 Mar;139(3):913-922. doi: 10.1016/j.jaci.2016.08.030. Epub 2016 Oct 3. J Allergy Clin Immunol. 2017. PMID: 27713077

4

Somatic Hypermutation Defects in Common Variable Immune Deficiency.

Almejun MB, Borge M. Almejun MB, et al. Curr Allergy Asthma Rep. 2017 Oct 5;17(11):76. doi: 10.1007/s11882-017-0745-7. Curr Allergy Asthma Rep. 2017. PMID: 28983794 Review.

5

Disease-associated CTNNBL1 mutation impairs somatic hypermutation by decreasing nuclear AID.

Kuhny M, Forbes LR, Çakan E, Vega-Loza A, Kostiuk V, Dinesh RK, Glauzy S, Stray-Pedersen A, Pezzi AE, Hanson IC, Vargas-Hernandez A, Xu ML, Coban-Akdemir ZH, Jhangiani SN, Muzny DM, Gibbs RA, Lupski JR, Chinn IK, Schatz DG, Orange JS, Meffre E. Kuhny M, et al. J Clin Invest. 2020 Aug 3;130(8):4411-4422. doi: 10.1172/JCI131297. J Clin Invest. 2020. PMID: 32484799 Free PMC article.

6

Altered spectrum of somatic hypermutation in common variable immunodeficiency disease characteristic of defective repair of mutations.

Duvvuri B, Duvvuri VR, Grigull J, Martin A, Pan-Hammarström Q, Wu GE, Larijani M. Duvvuri B, et al. Immunogenetics. 2011 Jan;63(1):1-11. doi: 10.1007/s00251-010-0483-7. Epub 2010 Oct 12. Immunogenetics. 2011. PMID: 20938659

7

Long-term follow-up on affinity maturation and memory B-cell generation in patients with common variable immunodeficiency.

Ballegaard V, Permin H, Katzenstein TL, Marquart HV, Schejbel L. Ballegaard V, et al. J Clin Immunol. 2013 Aug;33(6):1067-77. doi: 10.1007/s10875-013-9893-2. Epub 2013 May 7. J Clin Immunol. 2013. PMID: 23649616

8

Impaired antibody affinity maturation process characterizes a subset of patients with common variable immunodeficiency.

Bonhomme D, Hammarström L, Webster D, Chapel H, Hermine O, Le Deist F, Lepage E, Romeo PH, Levy Y. Bonhomme D, et al. J Immunol. 2000 Oct 15;165(8):4725-30. doi: 10.4049/jimmunol.165.8.4725. J Immunol. 2000. PMID: 11035117

9

ATM is not required in somatic hypermutation of VH, but is involved in the introduction of mutations in the switch mu region.

Pan-Hammarström Q, Dai S, Zhao Y, van Dijk-Härd IF, Gatti RA, Børresen-Dale AL, Hammarström L. Pan-Hammarström Q, et al. J Immunol. 2003 Apr 1;170(7):3707-16. doi: 10.4049/jimmunol.170.7.3707. J Immunol. 2003. PMID: 12646636

10

B-cell replication history and somatic hypermutation status identify distinct pathophysiologic backgrounds in common variable immunodeficiency.

Driessen GJ, van Zelm MC, van Hagen PM, Hartwig NG, Trip M, Warris A, de Vries E, Barendregt BH, Pico I, Hop W, van Dongen JJ, van der Burg M. Driessen GJ, et al. Blood. 2011 Dec 22;118(26):6814-23. doi: 10.1182/blood-2011-06-361881. Epub 2011 Oct 31. Blood. 2011. PMID: 22042693 Free article.

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