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

Year Number of Results
2005 1
2006 1
2007 1
2009 1
2011 2
2012 1
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2016 2
2017 5
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2023 3
2024 3

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Page 1
Pan-cancer analysis reveals the relationship between RCSD1 immune infiltration and clinical prognosis in human tumors.
Qiao H, Yin H, Feng Y, Tang H. Qiao H, et al. Front Immunol. 2022 Oct 13;13:1008778. doi: 10.3389/fimmu.2022.1008778. eCollection 2022. Front Immunol. 2022. PMID: 36311703 Free PMC article.
BACKGROUND: RCSD1 is a cytoskeletal regulator that has been confirmed to undergo genetic mutations in hematological tumors, but the mechanisms of RCSD1 in pan-cancer and its impact on patient prognosis have not been studied. ...The RCSD1 co-expression network …
BACKGROUND: RCSD1 is a cytoskeletal regulator that has been confirmed to undergo genetic mutations in hematological tumors, but the m …
RCSD1-ABL1 Translocation Associated with IKZF1 Gene Deletion in B-Cell Acute Lymphoblastic Leukemia.
Kamran S, Raca G, Nazir K. Kamran S, et al. Case Rep Hematol. 2015;2015:353247. doi: 10.1155/2015/353247. Epub 2015 Oct 27. Case Rep Hematol. 2015. PMID: 26600955 Free PMC article.
The RCSD1 gene has recently been identified as a novel gene fusion partner of the ABL1 gene in cases of B-cell Acute Lymphoblastic Leukemia (B-ALL). The RCSD1 gene is located at 1q23 and ABL1 is located at 9q34, so that the RCSD1-ABL1 fusion typically arises …
The RCSD1 gene has recently been identified as a novel gene fusion partner of the ABL1 gene in cases of B-cell Acute Lymphoblastic Le …
RCSD1-ABL1-positive B lymphoblastic leukemia is sensitive to dexamethasone and tyrosine kinase inhibitors and rapidly evolves clonally by chromosomal translocations.
Inokuchi K, Wakita S, Hirakawa T, Tamai H, Yokose N, Yamaguchi H, Dan K. Inokuchi K, et al. Int J Hematol. 2011 Sep;94(3):255-260. doi: 10.1007/s12185-011-0910-z. Epub 2011 Aug 24. Int J Hematol. 2011. PMID: 21863287
We performed breakpoint analysis of the transcript expressed by the RCSD1-ABL1 fusion gene. RT-PCR and sequence analyses detected transcription of a single RCSD1-ABL1 fusion gene variant, which had breakpoints in exon 3 of RCSD1 and exon 4 of ABL1. The RCS …
We performed breakpoint analysis of the transcript expressed by the RCSD1-ABL1 fusion gene. RT-PCR and sequence analyses detected tra …
The CapZ interacting protein Rcsd1 is required for cardiogenesis downstream of Wnt11a in Xenopus laevis.
Hempel A, Kühl SJ, Rothe M, Rao Tata P, Sirbu IO, Vainio SJ, Kühl M. Hempel A, et al. Dev Biol. 2017 Apr 1;424(1):28-39. doi: 10.1016/j.ydbio.2017.02.014. Epub 2017 Feb 22. Dev Biol. 2017. PMID: 28237811 Free article.
Using Xenopus as a model system, we show by loss of function and corresponding rescue experiments that the non-canonical Wnt signalling mediator Rcsd1 is required downstream of Wnt11 for ventricular trabeculation, terminal differentiation of cardiomyocytes and cardiac morp …
Using Xenopus as a model system, we show by loss of function and corresponding rescue experiments that the non-canonical Wnt signalling medi …
Genome-wide study of genetic polymorphisms predictive for outcome from first-line oxaliplatin-based chemotherapy in colorectal cancer patients.
Park HA, Edelmann D, Canzian F, Seibold P, Harrison TA, Hua X, Shi Q, Silverman A, Benner A, Macauda A, Schneider M, Goldberg RM, Alberts SR, Hoffmeister M, Brenner H, Chan AT, Peters U, Newcomb PA, Chang-Claude J. Park HA, et al. Int J Cancer. 2023 Nov 1;153(9):1623-1634. doi: 10.1002/ijc.34663. Epub 2023 Aug 4. Int J Cancer. 2023. PMID: 37539667

For mCRC patients, three loci on chr1 (rs1234556), chr12 (rs11052270) and chr15 (rs11858406) were found to be associated with differential OS (P < 5 10(-7) ). The locus on chr1 located in the intronic region of RCSD1 was replicated in an independent cohort of 586 mCRC p

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For mCRC patients, three loci on chr1 (rs1234556), chr12 (rs11052270) and chr15 (rs11858406) were found to be associated with differential O …
23 results