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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 1 |
2010 | 1 |
2016 | 1 |
2019 | 1 |
2021 | 1 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 9419
7 results
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Page 1
Biallelic variants in CRIPT cause a Rothmund-Thomson-like syndrome with increased cellular senescence.
Genet Med. 2023 Jul;25(7):100836. doi: 10.1016/j.gim.2023.100836. Epub 2023 Mar 31.
Genet Med. 2023.
PMID: 37013901
Free article.
Mitotic spindle disassembly in human cells relies on CRIPT having hierarchical redox signals.
Xu K, Wang C, Keinänen K, Li H, Cai C.
Xu K, et al.
J Cell Sci. 2022 Sep 15;135(18):jcs259657. doi: 10.1242/jcs.259657. Epub 2022 Sep 23.
J Cell Sci. 2022.
PMID: 36148798
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Divergent Evolution of a Protein-Protein Interaction Revealed through Ancestral Sequence Reconstruction and Resurrection.
Laursen L, Čalyševa J, Gibson TJ, Jemth P.
Laursen L, et al.
Mol Biol Evol. 2021 Jan 4;38(1):152-167. doi: 10.1093/molbev/msaa198.
Mol Biol Evol. 2021.
PMID: 32750125
Free PMC article.
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Intramolecular domain dynamics regulate synaptic MAGUK protein interactions.
Rademacher N, Kuropka B, Kunde SA, Wahl MC, Freund C, Shoichet SA.
Rademacher N, et al.
Elife. 2019 Mar 13;8:e41299. doi: 10.7554/eLife.41299.
Elife. 2019.
PMID: 30864948
Free PMC article.
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CRIPT exonic deletion and a novel missense mutation in a female with short stature, dysmorphic features, microcephaly, and pigmentary abnormalities.
Leduc MS, Niu Z, Bi W, Zhu W, Miloslavskaya I, Chiang T, Streff H, Seavitt JR, Murray SA, Eng C, Chan A, Yang Y, Lalani SR.
Leduc MS, et al.
Am J Med Genet A. 2016 Aug;170(8):2206-11. doi: 10.1002/ajmg.a.37780. Epub 2016 Jun 2.
Am J Med Genet A. 2016.
PMID: 27250922
Free PMC article.
Review.
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Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients.
Saus E, Brunet A, Armengol L, Alonso P, Crespo JM, Fernández-Aranda F, Guitart M, Martín-Santos R, Menchón JM, Navinés R, Soria V, Torrens M, Urretavizcaya M, Vallès V, Gratacòs M, Estivill X.
Saus E, et al.
J Psychiatr Res. 2010 Oct;44(14):971-8. doi: 10.1016/j.jpsychires.2010.03.007. Epub 2010 Apr 15.
J Psychiatr Res. 2010.
PMID: 20398908
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Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment.
Gratacòs M, Costas J, de Cid R, Bayés M, González JR, Baca-García E, de Diego Y, Fernández-Aranda F, Fernández-Piqueras J, Guitart M, Martín-Santos R, Martorell L, Menchón JM, Roca M, Sáiz-Ruiz J, Sanjuán J, Torrens M, Urretavizcaya M, Valero J, Vilella E, Estivill X, Carracedo A; Psychiatric Genetics Network Group.
Gratacòs M, et al.
Am J Med Genet B Neuropsychiatr Genet. 2009 Sep 5;150B(6):808-16. doi: 10.1002/ajmg.b.30902.
Am J Med Genet B Neuropsychiatr Genet. 2009.
PMID: 19086053
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