Imai K - Search Results

1

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study.

Coulter TI, Chandra A, Bacon CM, Babar J, Curtis J, Screaton N, Goodlad JR, Farmer G, Steele CL, Leahy TR, Doffinger R, Baxendale H, Bernatoniene J, Edgar JD, Longhurst HJ, Ehl S, Speckmann C, Grimbacher B, Sediva A, Milota T, Faust SN, Williams AP, Hayman G, Kucuk ZY, Hague R, French P, Brooker R, Forsyth P, Herriot R, Cancrini C, Palma P, Ariganello P, Conlon N, Feighery C, Gavin PJ, Jones A, Imai K, Ibrahim MA, Markelj G, Abinun M, Rieux-Laucat F, Latour S, Pellier I, Fischer A, Touzot F, Casanova JL, Durandy A, Burns SO, Savic S, Kumararatne DS, Moshous D, Kracker S, Vanhaesebroeck B, Okkenhaug K, Picard C, Nejentsev S, Condliffe AM, Cant AJ. Coulter TI, et al. Among authors: imai k. J Allergy Clin Immunol. 2017 Feb;139(2):597-606.e4. doi: 10.1016/j.jaci.2016.06.021. Epub 2016 Jul 16. J Allergy Clin Immunol. 2017. PMID: 27555459 Free PMC article.

2

Hyper-IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination.

Imai K, Catalan N, Plebani A, Maródi L, Sanal O, Kumaki S, Nagendran V, Wood P, Glastre C, Sarrot-Reynauld F, Hermine O, Forveille M, Revy P, Fischer A, Durandy A. Imai K, et al. J Clin Invest. 2003 Jul;112(1):136-42. doi: 10.1172/JCI18161. J Clin Invest. 2003. PMID: 12840068 Free PMC article.

3

The block in immunoglobulin class switch recombination caused by activation-induced cytidine deaminase deficiency occurs prior to the generation of DNA double strand breaks in switch mu region.

Catalan N, Selz F, Imai K, Revy P, Fischer A, Durandy A. Catalan N, et al. Among authors: imai k. J Immunol. 2003 Sep 1;171(5):2504-9. doi: 10.4049/jimmunol.171.5.2504. J Immunol. 2003. PMID: 12928399

4

Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.

Imai K, Slupphaug G, Lee WI, Revy P, Nonoyama S, Catalan N, Yel L, Forveille M, Kavli B, Krokan HE, Ochs HD, Fischer A, Durandy A. Imai K, et al. Nat Immunol. 2003 Oct;4(10):1023-8. doi: 10.1038/ni974. Epub 2003 Sep 7. Nat Immunol. 2003. PMID: 12958596

5

Hyper-immunoglobulin M syndromes caused by intrinsic B-lymphocyte defects.

Durandy A, Revy P, Imai K, Fischer A. Durandy A, et al. Among authors: imai k. Immunol Rev. 2005 Feb;203:67-79. doi: 10.1111/j.0105-2896.2005.00222.x. Immunol Rev. 2005. PMID: 15661022 Review.

6

Analysis of class switch recombination and somatic hypermutation in patients affected with autosomal dominant hyper-IgM syndrome type 2.

Imai K, Zhu Y, Revy P, Morio T, Mizutani S, Fischer A, Nonoyama S, Durandy A. Imai K, et al. Clin Immunol. 2005 Jun;115(3):277-85. doi: 10.1016/j.clim.2005.02.003. Clin Immunol. 2005. PMID: 15893695

7

B cells from hyper-IgM patients carrying UNG mutations lack ability to remove uracil from ssDNA and have elevated genomic uracil.

Kavli B, Andersen S, Otterlei M, Liabakk NB, Imai K, Fischer A, Durandy A, Krokan HE, Slupphaug G. Kavli B, et al. Among authors: imai k. J Exp Med. 2005 Jun 20;201(12):2011-21. doi: 10.1084/jem.20050042. J Exp Med. 2005. PMID: 15967827 Free PMC article.

8

X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options.

Albert MH, Bittner TC, Nonoyama S, Notarangelo LD, Burns S, Imai K, Espanol T, Fasth A, Pellier I, Strauss G, Morio T, Gathmann B, Noordzij JG, Fillat C, Hoenig M, Nathrath M, Meindl A, Pagel P, Wintergerst U, Fischer A, Thrasher AJ, Belohradsky BH, Ochs HD. Albert MH, et al. Among authors: imai k. Blood. 2010 Apr 22;115(16):3231-8. doi: 10.1182/blood-2009-09-239087. Epub 2010 Feb 19. Blood. 2010. PMID: 20173115 Free article.

9

Impaired induction of DNA lesions during immunoglobulin class-switch recombination in humans influences end-joining repair.

Kracker S, Imai K, Gardès P, Ochs HD, Fischer A, Durandy AH. Kracker S, et al. Among authors: imai k. Proc Natl Acad Sci U S A. 2010 Dec 21;107(51):22225-30. doi: 10.1073/pnas.1012591108. Epub 2010 Dec 6. Proc Natl Acad Sci U S A. 2010. PMID: 21135220 Free PMC article.

10

Clinical and genetic characteristics of XIAP deficiency in Japan.

Yang X, Kanegane H, Nishida N, Imamura T, Hamamoto K, Miyashita R, Imai K, Nonoyama S, Sanayama K, Yamaide A, Kato F, Nagai K, Ishii E, van Zelm MC, Latour S, Zhao XD, Miyawaki T. Yang X, et al. Among authors: imai k. J Clin Immunol. 2012 Jun;32(3):411-20. doi: 10.1007/s10875-011-9638-z. Epub 2012 Jan 8. J Clin Immunol. 2012. PMID: 22228567

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