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Page 1
Short-term mucosal disruption enables colibactin-producing E. coli to cause long-term perturbation of colonic homeostasis.
Gut Microbes. 2023 Jan-Dec;15(1):2233689. doi: 10.1080/19490976.2023.2233689.
Gut Microbes. 2023.
PMID: 37427832
Free PMC article.
R-spondin 3 promotes stem cell recovery and epithelial regeneration in the colon.
Harnack C, Berger H, Antanaviciute A, Vidal R, Sauer S, Simmons A, Meyer TF, Sigal M.
Harnack C, et al.
Nat Commun. 2019 Sep 25;10(1):4368. doi: 10.1038/s41467-019-12349-5.
Nat Commun. 2019.
PMID: 31554819
Free PMC article.
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Rare variants in NR2F2 cause congenital heart defects in humans.
Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LC, Swaminathan GJ, Bentham J, Arndt AK, Louw J, Low J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, Harnack C, Hoff K, Kramer HH, Schubert S, Siebert R, Toka O, Cosgrove C, Watkins H, Lucassen AM, O'Kelly IM, Salmon AP, Bu'lock FA, Granados-Riveron J, Setchfield K, Thornborough C, Brook JD, Mulder B, Klaassen S, Bhattacharya S, Devriendt K, Fitzpatrick DF; UK10K Consortium; Wilson DI, Mital S, Hurles ME.
Al Turki S, et al. Among authors: harnack c.
Am J Hum Genet. 2014 Apr 3;94(4):574-85. doi: 10.1016/j.ajhg.2014.03.007.
Am J Hum Genet. 2014.
PMID: 24702954
Free PMC article.
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Establishment, functional and genetic characterization of a colon derived large cell neuroendocrine carcinoma cell line.
Gock M, Mullins CS, Harnack C, Prall F, Ramer R, Göder A, Krämer OH, Klar E, Linnebacher M.
Gock M, et al. Among authors: harnack c.
World J Gastroenterol. 2018 Sep 7;24(33):3749-3759. doi: 10.3748/wjg.v24.i33.3749.
World J Gastroenterol. 2018.
PMID: 30197480
Free PMC article.
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Establishment and characterization of HROC69 - a Crohn´s related colonic carcinoma cell line and its matched patient-derived xenograft.
Kuehn F, Mullins CS, Krohn M, Harnack C, Ramer R, Krämer OH, Klar E, Huehns M, Linnebacher M.
Kuehn F, et al. Among authors: harnack c.
Sci Rep. 2016 Apr 18;6:24671. doi: 10.1038/srep24671.
Sci Rep. 2016.
PMID: 27087592
Free PMC article.
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Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.
Arndt AK, Schafer S, Drenckhahn JD, Sabeh MK, Plovie ER, Caliebe A, Klopocki E, Musso G, Werdich AA, Kalwa H, Heinig M, Padera RF, Wassilew K, Bluhm J, Harnack C, Martitz J, Barton PJ, Greutmann M, Berger F, Hubner N, Siebert R, Kramer HH, Cook SA, MacRae CA, Klaassen S.
Arndt AK, et al. Among authors: harnack c.
Am J Hum Genet. 2013 Jul 11;93(1):67-77. doi: 10.1016/j.ajhg.2013.05.015. Epub 2013 Jun 13.
Am J Hum Genet. 2013.
PMID: 23768516
Free PMC article.
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Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.
Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LCA, Swaminathan GJ, Bentham J, Arndt AK, Louw J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, Harnack C, Hoff K, Kramer HH, Schubert S, Siebert R, Toka O, Cosgrove C, Watkins H, Lucassen AM, O'Kelly IM, Salmon AP, Bu'Lock FA, Granados-Riveron J, Setchfield K, Thornborough C, Brook JD, Mulder B, Klaassen S, Bhattacharya S, Devriendt K, FitzPatrick DR; UK10K Consortium; Wilson DI, Mital S, Hurles ME.
Al Turki S, et al. Among authors: harnack c.
Am J Hum Genet. 2016 Mar 3;98(3):592. doi: 10.1016/j.ajhg.2016.02.016. Epub 2016 Mar 3.
Am J Hum Genet. 2016.
PMID: 28863274
Free PMC article.
No abstract available.
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