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Items: 23

1.

Transcriptomic Analysis Reveals Priming of The Host Antiviral Interferon Signaling Pathway by Bronchobini® Resulting in Balanced Immune Response to Rhinovirus Infection in Mouse Lung Tissue Slices.

Reamon-Buettner SM, Niehof M, Hirth N, Danov O, Obernolte H, Braun A, Warnecke J, Sewald K, Wronski S.

Int J Mol Sci. 2019 May 7;20(9). pii: E2242. doi: 10.3390/ijms20092242.

2.

Mechanisms underlying epigenetic and transcriptional heterogeneity in Chinese hamster ovary (CHO) cell lines.

Veith N, Ziehr H, MacLeod RA, Reamon-Buettner SM.

BMC Biotechnol. 2016 Jan 22;16:6. doi: 10.1186/s12896-016-0238-0.

3.

Identifying placental epigenetic alterations in an intrauterine growth restriction (IUGR) rat model induced by gestational protein deficiency.

Reamon-Buettner SM, Buschmann J, Lewin G.

Reprod Toxicol. 2014 Jun;45:117-24. doi: 10.1016/j.reprotox.2014.02.009. Epub 2014 Mar 5.

PMID:
24607647
4.

Transcriptional defect of an inherited NKX2-5 haplotype comprising a SNP, a nonsynonymous and a synonymous mutation, associated with human congenital heart disease.

Reamon-Buettner SM, Sattlegger E, Ciribilli Y, Inga A, Wessel A, Borlak J.

PLoS One. 2013 Dec 20;8(12):e83295. doi: 10.1371/journal.pone.0083295. eCollection 2013.

5.

Dissecting epigenetic silencing complexity in the mouse lung cancer suppressor gene Cadm1.

Reamon-Buettner SM, Borlak J.

PLoS One. 2012;7(6):e38531. doi: 10.1371/journal.pone.0038531. Epub 2012 Jun 6.

6.

NKX2-5: an update on this hypermutable homeodomain protein and its role in human congenital heart disease (CHD).

Reamon-Buettner SM, Borlak J.

Hum Mutat. 2010 Nov;31(11):1185-94. doi: 10.1002/humu.21345. Epub 2010 Oct 12. Review.

PMID:
20725931
7.

A functional genetic study identifies HAND1 mutations in septation defects of the human heart.

Reamon-Buettner SM, Ciribilli Y, Traverso I, Kuhls B, Inga A, Borlak J.

Hum Mol Genet. 2009 Oct 1;18(19):3567-78. doi: 10.1093/hmg/ddp305. Epub 2009 Jul 7.

PMID:
19586923
8.

Epigenetic silencing of cell adhesion molecule 1 in different cancer progenitor cells of transgenic c-Myc and c-Raf mouse lung tumors.

Reamon-Buettner SM, Borlak J.

Cancer Res. 2008 Sep 15;68(18):7587-96. doi: 10.1158/0008-5472.CAN-08-0967.

9.

The next innovation cycle in toxicogenomics: environmental epigenetics.

Reamon-Buettner SM, Mutschler V, Borlak J.

Mutat Res. 2008 Jul-Aug;659(1-2):158-65. doi: 10.1016/j.mrrev.2008.01.003. Epub 2008 Jan 19. Review.

PMID:
18342568
10.

A loss-of-function mutation in the binding domain of HAND1 predicts hypoplasia of the human hearts.

Reamon-Buettner SM, Ciribilli Y, Inga A, Borlak J.

Hum Mol Genet. 2008 May 15;17(10):1397-405. doi: 10.1093/hmg/ddn027. Epub 2008 Feb 14.

PMID:
18276607
11.

A new paradigm in toxicology and teratology: altering gene activity in the absence of DNA sequence variation.

Reamon-Buettner SM, Borlak J.

Reprod Toxicol. 2007 Jul;24(1):20-30. Epub 2007 May 22. Review.

PMID:
17596910
12.
13.

Somatic mutations in cardiac malformations.

Reamon-Buettner SM, Borlak J.

J Med Genet. 2006 Aug;43(8):e45. No abstract available.

14.

N-acetyltransferase 2 (NAT2) gene polymorphisms in colon and lung cancer patients.

Borlak J, Reamon-Buettner SM.

BMC Med Genet. 2006 Jul 9;7:58.

15.

Bridging the gap between anatomy and molecular genetics for an improved understanding of congenital heart disease.

Reamon-Buettner SM, Spanel-Borowski K, Borlak J.

Ann Anat. 2006 May;188(3):213-20. Review.

PMID:
16711160
16.

N-acetyltransferase 2 (NAT2) gene polymorphisms in Parkinson's disease.

Borlak J, Reamon-Buettner SM.

BMC Med Genet. 2006 Mar 29;7:30.

17.

HEY2 mutations in malformed hearts.

Reamon-Buettner SM, Borlak J.

Hum Mutat. 2006 Jan;27(1):118.

PMID:
16329098
18.

Functional dissection of sequence-specific NKX2-5 DNA binding domain mutations associated with human heart septation defects using a yeast-based system.

Inga A, Reamon-Buettner SM, Borlak J, Resnick MA.

Hum Mol Genet. 2005 Jul 15;14(14):1965-75. Epub 2005 May 25.

PMID:
15917268
19.

GATA4 zinc finger mutations as a molecular rationale for septation defects of the human heart.

Reamon-Buettner SM, Borlak J.

J Med Genet. 2005 May;42(5):e32. No abstract available.

20.

Genetic analysis of cardiac-specific transcription factors reveals novel insights into molecular causes of congenital heart disease.

Reamon-Buettner S, Borlak J.

Future Cardiol. 2005 May;1(3):355-61. doi: 10.1517/14796678.1.3.355.

PMID:
19804118
21.
22.

TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts.

Reamon-Buettner SM, Borlak J.

Hum Mutat. 2004 Jul;24(1):104.

PMID:
15221798
23.

Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations.

Reamon-Buettner SM, Hecker H, Spanel-Borowski K, Craatz S, Kuenzel E, Borlak J.

Am J Pathol. 2004 Jun;164(6):2117-25.

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