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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1994 | 1 |
1996 | 1 |
1997 | 1 |
2011 | 1 |
2016 | 1 |
2017 | 1 |
2024 | 0 |
PubMed (cited) for id: 602486
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Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia.
Clin Genet. 2017 Jul;92(1):91-98. doi: 10.1111/cge.12964. Epub 2017 Feb 22.
Clin Genet. 2017.
PMID: 28067412
Free article.
Further evidence of POP1 mutations as the cause of anauxetic dysplasia.
Elalaoui SC, Laarabi FZ, Mansouri M, Mrani NA, Nishimura G, Sefiani A.
Elalaoui SC, et al.
Am J Med Genet A. 2016 Sep;170(9):2462-5. doi: 10.1002/ajmg.a.37839. Epub 2016 Jul 6.
Am J Med Genet A. 2016.
PMID: 27380734
Item in Clipboard
Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia.
Glazov EA, Zankl A, Donskoi M, Kenna TJ, Thomas GP, Clark GR, Duncan EL, Brown MA.
Glazov EA, et al.
PLoS Genet. 2011 Mar;7(3):e1002027. doi: 10.1371/journal.pgen.1002027. Epub 2011 Mar 24.
PLoS Genet. 2011.
PMID: 21455487
Free PMC article.
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A bidirectional promoter connects the p14.5 gene to the gene for RNase P and RNase MRP protein subunit hPOP1.
Schmiedeknecht G, Büchler C, Schmitz G.
Schmiedeknecht G, et al.
Biochem Biophys Res Commun. 1997 Dec 8;241(1):59-67. doi: 10.1006/bbrc.1997.7772.
Biochem Biophys Res Commun. 1997.
PMID: 9405234
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hPop1: an autoantigenic protein subunit shared by the human RNase P and RNase MRP ribonucleoproteins.
Lygerou Z, Pluk H, van Venrooij WJ, Séraphin B.
Lygerou Z, et al.
EMBO J. 1996 Nov 1;15(21):5936-48.
EMBO J. 1996.
PMID: 8918471
Free PMC article.
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The POP1 gene encodes a protein component common to the RNase MRP and RNase P ribonucleoproteins.
Lygerou Z, Mitchell P, Petfalski E, Séraphin B, Tollervey D.
Lygerou Z, et al.
Genes Dev. 1994 Jun 15;8(12):1423-33. doi: 10.1101/gad.8.12.1423.
Genes Dev. 1994.
PMID: 7926742
Free article.
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