Krooss SA - Search Results

1

Ex Vivo/In vivo Gene Editing in Hepatocytes Using "All-in-One" CRISPR-Adeno-Associated Virus Vectors with a Self-Linearizing Repair Template.

Krooss SA, Dai Z, Schmidt F, Rovai A, Fakhiri J, Dhingra A, Yuan Q, Yang T, Balakrishnan A, Steinbrück L, Srivaratharajan S, Manns MP, Schambach A, Grimm D, Bohne J, Sharma AD, Büning H, Ott M. Krooss SA, et al. iScience. 2020 Jan 24;23(1):100764. doi: 10.1016/j.isci.2019.100764. Epub 2019 Dec 12. iScience. 2020. PMID: 31887661 Free PMC article.

2

Homologous recombination mediates stable Fah gene integration and phenotypic correction in tyrosinaemia mouse-model.

Junge N, Yuan Q, Vu TH, Krooss S, Bednarski C, Balakrishnan A, Cathomen T, Manns MP, Baumann U, Sharma AD, Ott M. Junge N, et al. World J Hepatol. 2018 Feb 27;10(2):277-286. doi: 10.4254/wjh.v10.i2.277. World J Hepatol. 2018. PMID: 29527263 Free PMC article.

3

In vivo adenine base editing reverts C282Y and improves iron metabolism in hemochromatosis mice.

Rovai A, Chung B, Hu Q, Hook S, Yuan Q, Kempf T, Schmidt F, Grimm D, Talbot SR, Steinbrück L, Götting J, Bohne J, Krooss SA, Ott M. Rovai A, et al. Among authors: krooss sa. Nat Commun. 2022 Sep 5;13(1):5215. doi: 10.1038/s41467-022-32906-9. Nat Commun. 2022. PMID: 36064805 Free PMC article.

4

Pathological mechanism and antisense oligonucleotide-mediated rescue of a non-coding variant suppressing factor 9 RNA biogenesis leading to hemophilia B.

Krooss S, Werwitzke S, Kopp J, Rovai A, Varnholt D, Wachs AS, Goyenvalle A, Aarstma-Rus A, Ott M, Tiede A, Langemeier J, Bohne J. Krooss S, et al. PLoS Genet. 2020 Apr 8;16(4):e1008690. doi: 10.1371/journal.pgen.1008690. eCollection 2020 Apr. PLoS Genet. 2020. PMID: 32267853 Free PMC article.

5

Identification of the Cleavage Domain within Glycoprotein G of Herpes Simplex Virus Type 2.

Kropp KA, Srivaratharajan S, Ritter B, Yu P, Krooss S, Polten F, Pich A, Alcami A, Viejo-Borbolla A. Kropp KA, et al. Viruses. 2020 Dec 12;12(12):1428. doi: 10.3390/v12121428. Viruses. 2020. PMID: 33322659 Free PMC article.

6

Correction: Pathological mechanism and antisense oligonucleotide-mediated rescue of a non-coding variant suppressing factor 9 RNA biogenesis leading to hemophilia B.

Krooss S, Werwitzke S, Kopp J, Rovai A, Varnholt D, Wachs AS, Goyenvalle A, Aartsma-Rus A, Ott M, Tiede A, Langemeier J, Bohne J. Krooss S, et al. PLoS Genet. 2021 Jan 28;17(1):e1009345. doi: 10.1371/journal.pgen.1009345. eCollection 2021 Jan. PLoS Genet. 2021. PMID: 33507897 Free PMC article.

7

Homozygous frame shift variant in ATP7B exon 1 leads to bypass of nonsense-mediated mRNA decay and to a protein capable of copper export.

Stalke A, Pfister ED, Baumann U, Eilers M, Schäffer V, Illig T, Auber B, Schlegelberger B, Brackmann R, Prokisch H, Krooss S, Bohne J, Skawran B. Stalke A, et al. Eur J Hum Genet. 2019 Jun;27(6):879-887. doi: 10.1038/s41431-019-0345-1. Epub 2019 Feb 5. Eur J Hum Genet. 2019. PMID: 30723317 Free PMC article.

8

The combined repetitive oligopeptides of clostridium difficile toxin A counteract premature cleavage of the glucosyl-transferase domain by stabilizing protein conformation.

Olling A, Hüls C, Goy S, Müller M, Krooss S, Rudolf I, Tatge H, Gerhard R. Olling A, et al. Toxins (Basel). 2014 Jul 22;6(7):2162-76. doi: 10.3390/toxins6072162. Toxins (Basel). 2014. PMID: 25054784 Free PMC article.

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