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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 4
2009 3
2010 4
2011 2
2013 2
2014 5
2015 3
2016 1
2017 2
2018 1
2019 2
2020 3
2021 0
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27 results
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Page 1
Differentiation Protocol for 3D Retinal Organoids, Immunostaining and Signal Quantitation.
Döpper H, Menges J, Bozet M, Brenzel A, Lohmann D, Steenpass L, Kanber D. Döpper H, et al. Among authors: kanber d. Curr Protoc Stem Cell Biol. 2020 Dec;55(1):e120. doi: 10.1002/cpsc.120. Curr Protoc Stem Cell Biol. 2020. PMID: 32956559
Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC lines.
Döpper H, Horstmann M, Menges J, Bozet M, Kanber D, Steenpass L. Döpper H, et al. Among authors: kanber d. Stem Cell Res. 2020 May;45:101779. doi: 10.1016/j.scr.2020.101779. Epub 2020 Mar 29. Stem Cell Res. 2020. PMID: 32268247 Free article.
Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes.
Beygo J, Buiting K, Ramsden SC, Ellis R, Clayton-Smith J, Kanber D. Beygo J, et al. Among authors: kanber d. Eur J Hum Genet. 2019 Sep;27(9):1326-1340. doi: 10.1038/s41431-019-0435-0. Epub 2019 Jun 24. Eur J Hum Genet. 2019. PMID: 31235867 Free PMC article.
Protective effect of hyperbaric oxygen treatment on rat intestinal mucosa after mesenteric ischaemia and reperfusion.
Açiksari K, Eğin S, Hepgül G, Mirasoğlu B, Tanriverdi G, Kanber DS, Demirci S, Doğan H, Özüçelik DN, Toklu AS, Seçkin İ, Yanar HT. Açiksari K, et al. Among authors: kanber ds. Diving Hyperb Med. 2019 Dec 20;49(4):253-258. doi: 10.28920/dhm49.4.253-258. Diving Hyperb Med. 2019. PMID: 31828743 Free PMC article.
13q deletion syndrome resulting from balanced chromosomal rearrangement in father: the significance of parental karyotyping.
Dittner-Moormann S, Reschke M, Biewald E, Kuechler A, Klein B, Timmermann B, Lohmann D, Ketteler P, Kanber D. Dittner-Moormann S, et al. Among authors: kanber d. Mol Cytogenet. 2020 Jul 23;13:31. doi: 10.1186/s13039-020-00500-7. eCollection 2020. Mol Cytogenet. 2020. PMID: 32760450 Free PMC article.
Imprinting of RB1 (the new kid on the block).
Buiting K, Kanber D, Horsthemke B, Lohmann D. Buiting K, et al. Among authors: kanber d. Brief Funct Genomics. 2010 Jul;9(4):347-53. doi: 10.1093/bfgp/elq014. Epub 2010 Jun 15. Brief Funct Genomics. 2010. PMID: 20551090 Review.
Generation of heterozygous and homozygous hESC H9 sublines carrying inactivating mutations in RB1.
Schipper L, Kanber D, Steenpass L. Schipper L, et al. Among authors: kanber d. Stem Cell Res. 2018 Dec;33:41-45. doi: 10.1016/j.scr.2018.09.016. Epub 2018 Sep 26. Stem Cell Res. 2018. PMID: 30312872 Free article.
The origin of the RB1 imprint.
Kanber D, Buiting K, Roos C, Gromoll J, Kaya S, Horsthemke B, Lohmann D. Kanber D, et al. PLoS One. 2013 Nov 25;8(11):e81502. doi: 10.1371/journal.pone.0081502. eCollection 2013. PLoS One. 2013. PMID: 24282601 Free PMC article.
Clinical utility gene card for: Prader-Willi Syndrome.
Buiting K, Cassidy SB, Driscoll DJ, Gillessen-Kaesbach G, Kanber D, Tauber M, Schwinger E, Horsthemke B. Buiting K, et al. Among authors: kanber d. Eur J Hum Genet. 2014 Sep;22(9). doi: 10.1038/ejhg.2014.66. Epub 2014 Apr 16. Eur J Hum Genet. 2014. PMID: 24736734 Free PMC article. No abstract available.
Clinical utility gene card for: Angelman Syndrome.
Buiting K, Clayton-Smith J, Driscoll DJ, Gillessen-Kaesbach G, Kanber D, Schwinger E, Williams C, Horsthemke B. Buiting K, et al. Among authors: kanber d. Eur J Hum Genet. 2015 Feb;23(2). doi: 10.1038/ejhg.2014.93. Epub 2014 Jun 4. Eur J Hum Genet. 2015. PMID: 24896151 Free PMC article. No abstract available.
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