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Items: 1 to 20 of 124

1.

Viperin mRNA is a novel target for the human RNase MRP/RNase P endoribonuclease.

Mattijssen S, Hinson ER, Onnekink C, Hermanns P, Zabel B, Cresswell P, Pruijn GJ.

Cell Mol Life Sci. 2011 Jul;68(14):2469-80. doi: 10.1007/s00018-010-0568-3. Epub 2010 Oct 30.

2.

RNase MRP and disease.

Mattijssen S, Welting TJ, Pruijn GJ.

Wiley Interdiscip Rev RNA. 2010 Jul-Aug;1(1):102-16. doi: 10.1002/wrna.9. Epub 2010 May 6. Review.

PMID:
21956908
3.

Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia.

Ridanpää M, van Eenennaam H, Pelin K, Chadwick R, Johnson C, Yuan B, vanVenrooij W, Pruijn G, Salmela R, Rockas S, Mäkitie O, Kaitila I, de la Chapelle A.

Cell. 2001 Jan 26;104(2):195-203.

4.

Small RNAs derived from lncRNA RNase MRP have gene-silencing activity relevant to human cartilage-hair hypoplasia.

Rogler LE, Kosmyna B, Moskowitz D, Bebawee R, Rahimzadeh J, Kutchko K, Laederach A, Notarangelo LD, Giliani S, Bouhassira E, Frenette P, Roy-Chowdhury J, Rogler CE.

Hum Mol Genet. 2014 Jan 15;23(2):368-82. doi: 10.1093/hmg/ddt427. Epub 2013 Sep 5.

5.

The molecular basis of the cartilage-hair hypoplasia-anauxetic dysplasia spectrum.

Thiel CT, Rauch A.

Best Pract Res Clin Endocrinol Metab. 2011 Feb;25(1):131-42. doi: 10.1016/j.beem.2010.08.004. Review.

PMID:
21396580
6.

RNA-protein interactions in the human RNase MRP ribonucleoprotein complex.

Pluk H, van Eenennaam H, Rutjes SA, Pruijn GJ, van Venrooij WJ.

RNA. 1999 Apr;5(4):512-24.

7.

Differential association of protein subunits with the human RNase MRP and RNase P complexes.

Welting TJ, Kikkert BJ, van Venrooij WJ, Pruijn GJ.

RNA. 2006 Jul;12(7):1373-82. Epub 2006 May 24.

9.

Identity of the RNase MRP- and RNase P-associated Th/To autoantigen.

Van Eenennaam H, Vogelzangs JH, Lugtenberg D, Van Den Hoogen FH, Van Venrooij WJ, Pruijn GJ.

Arthritis Rheum. 2002 Dec;46(12):3266-72.

10.
11.

Functional characterization of the conserved amino acids in Pop1p, the largest common protein subunit of yeast RNases P and MRP.

Xiao S, Hsieh J, Nugent RL, Coughlin DJ, Fierke CA, Engelke DR.

RNA. 2006 Jun;12(6):1023-37. Epub 2006 Apr 17.

12.

An infant with cartilage-hair hypoplasia due to a novel homozygous mutation in the promoter region of the RMRP gene associated with chondrodysplasia and severe immunodeficiency.

Vatanavicharn N, Visitsunthorn N, Pho-iam T, Jirapongsananuruk O, Pacharn P, Chokephaibulkit K, Limwongse C, Wasant P.

J Appl Genet. 2010;51(4):523-8. doi: 10.1007/BF03208884.

PMID:
21063072
13.

Basic domains target protein subunits of the RNase MRP complex to the nucleolus independently of complex association.

van Eenennaam H, van der Heijden A, Janssen RJ, van Venrooij WJ, Pruijn GJ.

Mol Biol Cell. 2001 Nov;12(11):3680-9.

14.

RNase MRP RNA and human genetic diseases.

Martin AN, Li Y.

Cell Res. 2007 Mar;17(3):219-26. Review.

15.

Cartilage-hair hypoplasia-associated mutations in the RNase MRP P3 domain affect RNA folding and ribonucleoprotein assembly.

Welting TJ, Mattijssen S, Peters FM, van Doorn NL, Dekkers L, van Venrooij WJ, Heus HA, Bonafé L, Pruijn GJ.

Biochim Biophys Acta. 2008 Mar;1783(3):455-66. doi: 10.1016/j.bbamcr.2007.11.016. Epub 2007 Dec 8.

16.

Type and level of RMRP functional impairment predicts phenotype in the cartilage hair hypoplasia-anauxetic dysplasia spectrum.

Thiel CT, Mortier G, Kaitila I, Reis A, Rauch A.

Am J Hum Genet. 2007 Sep;81(3):519-29. Epub 2007 Aug 6.

17.

Foetal presentation of cartilage hair hypoplasia with extensive granulomatous inflammation.

Crahes M, Saugier-Veber P, Patrier S, Aziz M, Pirot N, Brasseur-Daudruy M, Layet V, Frébourg T, Laquerrière A.

Eur J Med Genet. 2013 Jul;56(7):365-70. doi: 10.1016/j.ejmg.2013.04.004. Epub 2013 May 2.

PMID:
23643676
18.

Conserved and variable domains of RNase MRP RNA.

Dávila López M, Rosenblad MA, Samuelsson T.

RNA Biol. 2009 Jul-Aug;6(3):208-20. Epub 2009 Jul 30. Review.

PMID:
19395864
19.

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.

Genes Dev. 1994 Jun 15;8(12):1423-33.

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