Jäger AC - Search Results

1

Hereditary non-polyposis colorectal cancer (HNPCC): phenotype-genotype correlation between patients with and without identified mutation.

Bisgaard ML, Jäger AC, Myrhøj T, Bernstein I, Nielsen FC. Bisgaard ML, et al. Among authors: jager ac. Hum Mutat. 2002 Jul;20(1):20-7. doi: 10.1002/humu.10083. Hum Mutat. 2002. PMID: 12112654

2

Presymptomatic diagnosis using a deletion of a single codon in families with hereditary non-polyposis colorectal cancer.

Ripa RS, Katballe N, Wikman FP, Jäger AC, Bernstein I, Orntoft T, Schwartz M, Nielsen FC, Bisgaard ML. Ripa RS, et al. Among authors: jager ac. Mutat Res. 2005 Feb 15;570(1):89-96. doi: 10.1016/j.mrfmmm.2004.10.002. Mutat Res. 2005. PMID: 15680406

3

Functional characterization of MLH1 missense variants identified in Lynch syndrome patients.

Andersen SD, Liberti SE, Lützen A, Drost M, Bernstein I, Nilbert M, Dominguez M, Nyström M, Hansen TV, Christoffersen JW, Jäger AC, de Wind N, Nielsen FC, Tørring PM, Rasmussen LJ. Andersen SD, et al. Among authors: jager ac. Hum Mutat. 2012 Dec;33(12):1647-55. doi: 10.1002/humu.22153. Epub 2012 Jul 23. Hum Mutat. 2012. PMID: 22753075

4

Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression.

Jäger AC, Bisgaard ML, Myrhøj T, Bernstein I, Rehfeld JF, Nielsen FC. Jäger AC, et al. Am J Hum Genet. 1997 Jul;61(1):129-38. doi: 10.1086/513896. Am J Hum Genet. 1997. PMID: 9245993 Free PMC article.

5

Characterization of human exonuclease 1 in complex with mismatch repair proteins, subcellular localization and association with PCNA.

Nielsen FC, Jäger AC, Lützen A, Bundgaard JR, Rasmussen LJ. Nielsen FC, et al. Among authors: jager ac. Oncogene. 2004 Feb 19;23(7):1457-68. doi: 10.1038/sj.onc.1207265. Oncogene. 2004. PMID: 14676842

6

Allelic loss of chromosome 2p21-16.3 is associated with reduced survival in sporadic colorectal cancer.

Bisgaard ML, Jäger AC, Dalgaard P, Søndergaard JO, Rehfeld JF, Nielsen FC. Bisgaard ML, et al. Among authors: jager ac. Scand J Gastroenterol. 2001 Apr;36(4):405-9. doi: 10.1080/003655201300051252. Scand J Gastroenterol. 2001. PMID: 11336166

7

HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes.

Jäger AC, Rasmussen M, Bisgaard HC, Singh KK, Nielsen FC, Rasmussen LJ. Jäger AC, et al. Oncogene. 2001 Jun 14;20(27):3590-5. doi: 10.1038/sj.onc.1204467. Oncogene. 2001. PMID: 11429708

8

Characteristics of the Danish families with multiple endocrine neoplasia type 1.

Jäger AC, Friis-Hansen L, Hansen TV, Eskildsen PC, Sølling K, Knigge U, Hansen CP, Andersen PH, Brixen K, Feldt-Rasmussen U, Kroustrup JP, Mollerup CL, Rehfeld JF, Blichert-Toft M, Nielsen FC. Jäger AC, et al. Mol Cell Endocrinol. 2006 Apr 25;249(1-2):123-32. doi: 10.1016/j.mce.2006.02.008. Epub 2006 Mar 23. Mol Cell Endocrinol. 2006. PMID: 16563611

9

Is thyroidectomy necessary in RET mutations carriers of the familial medullary thyroid carcinoma syndrome?

Hansen HS, Torring H, Godballe C, Jäger AC, Nielsen FC. Hansen HS, et al. Among authors: jager ac. Cancer. 2000 Aug 15;89(4):863-7. Cancer. 2000. PMID: 10951350

10

Characterization of the human laminin beta2 chain locus (LAMB2): linkage to a gene containing a nonprocessed, transcribed LAMB2-like pseudogene (LAMB2L) and to the gene encoding glutaminyl tRNA synthetase (QARS).

Durkin ME, Jäger AC, Khurana TS, Nielsen FC, Albrechtsen R, Wewer UM. Durkin ME, et al. Among authors: jager ac. Cytogenet Cell Genet. 1999;84(3-4):173-8. doi: 10.1159/000015249. Cytogenet Cell Genet. 1999. PMID: 10393422

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