Garred P - Search Results

1

Molecular basis of hereditary C1q deficiency--revisited: identification of several novel disease-causing mutations.

Schejbel L, Skattum L, Hagelberg S, Åhlin A, Schiller B, Berg S, Genel F, Truedsson L, Garred P. Schejbel L, et al. Among authors: garred p. Genes Immun. 2011 Dec;12(8):626-34. doi: 10.1038/gene.2011.39. Epub 2011 Jun 9. Genes Immun. 2011. PMID: 21654842

2

Association of mannose-binding lectin gene variation with disease severity and infections in a population-based cohort of systemic lupus erythematosus patients.

Garred P, Voss A, Madsen HO, Junker P. Garred P, et al. Genes Immun. 2001 Dec;2(8):442-50. doi: 10.1038/sj.gene.6363804. Genes Immun. 2001. PMID: 11781711

3

Disease-associated mutations in human mannose-binding lectin compromise oligomerization and activity of the final protein.

Larsen F, Madsen HO, Sim RB, Koch C, Garred P. Larsen F, et al. Among authors: garred p. J Biol Chem. 2004 May 14;279(20):21302-11. doi: 10.1074/jbc.M400520200. Epub 2004 Feb 5. J Biol Chem. 2004. PMID: 14764589 Free article.

4

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. Among authors: garred p. 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.

5

Mannose-binding lectin and its genetic variants.

Garred P, Larsen F, Seyfarth J, Fujita R, Madsen HO. Garred P, et al. Genes Immun. 2006 Mar;7(2):85-94. doi: 10.1038/sj.gene.6364283. Genes Immun. 2006. PMID: 16395391 Review.

6

Primary immunodeficiency: complex genetic disorders?

Schejbel L, Garred P. Schejbel L, et al. Among authors: garred p. Clin Chem. 2007 Feb;53(2):159-60. doi: 10.1373/clinchem.2006.081224. Clin Chem. 2007. PMID: 17259244 No abstract available.

7

C1q deficiency in an Inuit family: identification of a new class of C1q disease-causing mutations.

Marquart HV, Schejbel L, Sjoholm A, Martensson U, Nielsen S, Koch A, Svejgaard A, Garred P. Marquart HV, et al. Among authors: garred p. Clin Immunol. 2007 Jul;124(1):33-40. doi: 10.1016/j.clim.2007.03.547. Epub 2007 May 21. Clin Immunol. 2007. PMID: 17513176

8

Properdin deficiency associated with recurrent otitis media and pneumonia, and identification of male carrier with Klinefelter syndrome.

Schejbel L, Rosenfeldt V, Marquart H, Valerius NH, Garred P. Schejbel L, et al. Among authors: garred p. Clin Immunol. 2009 Jun;131(3):456-62. doi: 10.1016/j.clim.2009.02.008. Epub 2009 Mar 27. Clin Immunol. 2009. PMID: 19328743

9

Association of HMGB1 polymorphisms with outcome after allogeneic hematopoietic cell transplantation.

Kornblit B, Masmas T, Petersen SL, Madsen HO, Heilmann C, Schejbel L, Sengeløv H, Müller K, Garred P, Vindeløv L. Kornblit B, et al. Among authors: garred p. Biol Blood Marrow Transplant. 2010 Feb;16(2):239-52. doi: 10.1016/j.bbmt.2009.10.002. Epub 2009 Oct 9. Biol Blood Marrow Transplant. 2010. PMID: 19819342 Free article.

10

The genetics of ficolins.

Garred P, Honoré C, Ma YJ, Rørvig S, Cowland J, Borregaard N, Hummelshøj T. Garred P, et al. J Innate Immun. 2010;2(1):3-16. doi: 10.1159/000242419. Epub 2009 Sep 24. J Innate Immun. 2010. PMID: 20375618 Free article. Review.

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