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Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.
Cancer Cell. 2019 Feb 11;35(2):256-266.e5. doi: 10.1016/j.ccell.2018.12.011.
Cancer Cell. 2019.
PMID: 30753826
Free article.
Monoallelic NTHL1 Loss-of-Function Variants and Risk of Polyposis and Colorectal Cancer.
Elsayed FA, Grolleman JE, Ragunathan A; NTHL1 study group; Buchanan DD, van Wezel T, de Voer RM.
Elsayed FA, et al. Among authors: grolleman je.
Gastroenterology. 2020 Dec;159(6):2241-2243.e6. doi: 10.1053/j.gastro.2020.08.042. Epub 2020 Aug 26.
Gastroenterology. 2020.
PMID: 32860789
Free PMC article.
No abstract available.
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Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancer.
Drost J, van Boxtel R, Blokzijl F, Mizutani T, Sasaki N, Sasselli V, de Ligt J, Behjati S, Grolleman JE, van Wezel T, Nik-Zainal S, Kuiper RP, Cuppen E, Clevers H.
Drost J, et al. Among authors: grolleman je.
Science. 2017 Oct 13;358(6360):234-238. doi: 10.1126/science.aao3130. Epub 2017 Sep 14.
Science. 2017.
PMID: 28912133
Free PMC article.
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Somatic mutational signatures in polyposis and colorectal cancer.
Grolleman JE, Díaz-Gay M, Franch-Expósito S, Castellví-Bel S, de Voer RM.
Grolleman JE, et al.
Mol Aspects Med. 2019 Oct;69:62-72. doi: 10.1016/j.mam.2019.05.002. Epub 2019 May 23.
Mol Aspects Med. 2019.
PMID: 31108140
Free article.
Review.
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Germline MBD4 deficiency causes a multi-tumor predisposition syndrome.
Palles C, West HD, Chew E, Galavotti S, Flensburg C, Grolleman JE, Jansen EAM, Curley H, Chegwidden L, Arbe-Barnes EH, Lander N, Truscott R, Pagan J, Bajel A, Sherwood K, Martin L, Thomas H, Georgiou D, Fostira F, Goldberg Y, Adams DJ, van der Biezen SAM, Christie M, Clendenning M, Thomas LE, Deltas C, Dimovski AJ, Dymerska D, Lubinski J, Mahmood K, van der Post RS, Sanders M, Weitz J, Taylor JC, Turnbull C, Vreede L, van Wezel T, Whalley C, Arnedo-Pac C, Caravagna G, Cross W, Chubb D, Frangou A, Gruber AJ, Kinnersley B, Noyvert B, Church D, Graham T, Houlston R, Lopez-Bigas N, Sottoriva A, Wedge D; Genomics England Research Consortium; CORGI Consortium; WGS500 Consortium; Jenkins MA, Kuiper RP, Roberts AW, Cheadle JP, Ligtenberg MJL, Hoogerbrugge N, Koelzer VH, Rivas AD, Winship IM, Ponte CR, Buchanan DD, Power DG, Green A, Tomlinson IPM, Sampson JR, Majewski IJ, de Voer RM.
Palles C, et al. Among authors: grolleman je.
Am J Hum Genet. 2022 May 5;109(5):953-960. doi: 10.1016/j.ajhg.2022.03.018. Epub 2022 Apr 22.
Am J Hum Genet. 2022.
PMID: 35460607
Free PMC article.
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Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing.
Lorca V, Rueda D, Martín-Morales L, Fernández-Aceñero MJ, Grolleman J, Poves C, Llovet P, Tapial S, García-Barberán V, Sanz J, Pérez-Segura P, de Voer RM, Díaz-Rubio E, de la Hoya M, Caldés T, Garre P.
Lorca V, et al.
Sci Rep. 2019 Jul 8;9(1):9814. doi: 10.1038/s41598-019-46403-5.
Sci Rep. 2019.
PMID: 31285513
Free PMC article.
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Shear stress induces expression, intracellular reorganization and enhanced Notch activation potential of Jagged1.
Driessen RCH, Stassen OMJA, Sjöqvist M, Suarez Rodriguez F, Grolleman J, Bouten CVC, Sahlgren CM.
Driessen RCH, et al.
Integr Biol (Camb). 2018 Nov 12;10(11):719-726. doi: 10.1039/c8ib00036k.
Integr Biol (Camb). 2018.
PMID: 30328449
Free PMC article.
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The hypoxia-response pathway modulates RAS/MAPK-mediated cell fate decisions in Caenorhabditis elegans.
Maxeiner S, Grolleman J, Schmid T, Kammenga J, Hajnal A.
Maxeiner S, et al.
Life Sci Alliance. 2019 May 24;2(3):e201800255. doi: 10.26508/lsa.201800255. Print 2019 Jun.
Life Sci Alliance. 2019.
PMID: 31126994
Free PMC article.
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