MBNL1

MBNL1

Muscleblind-like (Drosophila), also known as MBNL1, is a human gene.cite web | title = Entrez Gene: MBNL1 muscleblind-like (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4154| accessdate = ]

PBB_Summary
section_title =
summary_text =

References

Further reading

PBB_Further_reading
citations =
*cite journal | author=Bonaldo MF, Lennon G, Soares MB |title=Normalization and subtraction: two approaches to facilitate gene discovery. |journal=Genome Res. |volume=6 |issue= 9 |pages= 791–806 |year= 1997 |pmid= 8889548 |doi=
*cite journal | author=Ishikawa K, Nagase T, Nakajima D, "et al." |title=Prediction of the coding sequences of unidentified human genes. VIII. 78 new cDNA clones from brain which code for large proteins in vitro. |journal=DNA Res. |volume=4 |issue= 5 |pages= 307–13 |year= 1998 |pmid= 9455477 |doi=
*cite journal | author=Miller JW, Urbinati CR, Teng-Umnuay P, "et al." |title=Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy. |journal=EMBO J. |volume=19 |issue= 17 |pages= 4439–48 |year= 2000 |pmid= 10970838 |doi= 10.1093/emboj/19.17.4439
*cite journal | author=Fardaei M, Larkin K, Brook JD, Hamshere MG |title=In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts. |journal=Nucleic Acids Res. |volume=29 |issue= 13 |pages= 2766–71 |year= 2001 |pmid= 11433021 |doi=
*cite journal | author=Mankodi A, Urbinati CR, Yuan QP, "et al." |title=Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2. |journal=Hum. Mol. Genet. |volume=10 |issue= 19 |pages= 2165–70 |year= 2001 |pmid= 11590133 |doi=
*cite journal | author=Fardaei M, Rogers MT, Thorpe HM, "et al." |title=Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells. |journal=Hum. Mol. Genet. |volume=11 |issue= 7 |pages= 805–14 |year= 2002 |pmid= 11929853 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Kino Y, Mori D, Oma Y, "et al." |title=Muscleblind protein, MBNL1/EXP, binds specifically to CHHG repeats. |journal=Hum. Mol. Genet. |volume=13 |issue= 5 |pages= 495–507 |year= 2004 |pmid= 14722159 |doi= 10.1093/hmg/ddh056
*cite journal | author=Ho TH, Charlet-B N, Poulos MG, "et al." |title=Muscleblind proteins regulate alternative splicing. |journal=EMBO J. |volume=23 |issue= 15 |pages= 3103–12 |year= 2005 |pmid= 15257297 |doi= 10.1038/sj.emboj.7600300
*cite journal | author=Dansithong W, Paul S, Comai L, Reddy S |title=MBNL1 is the primary determinant of focus formation and aberrant insulin receptor splicing in DM1. |journal=J. Biol. Chem. |volume=280 |issue= 7 |pages= 5773–80 |year= 2005 |pmid= 15546872 |doi= 10.1074/jbc.M410781200
*cite journal | author=Ho TH, Savkur RS, Poulos MG, "et al." |title=Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy. |journal=J. Cell. Sci. |volume=118 |issue= Pt 13 |pages= 2923–33 |year= 2005 |pmid= 15961406 |doi= 10.1242/jcs.02404
*cite journal | author=Adereth Y, Dammai V, Kose N, "et al." |title=RNA-dependent integrin alpha3 protein localization regulated by the Muscleblind-like protein MLP1. |journal=Nat. Cell Biol. |volume=7 |issue= 12 |pages= 1240–7 |year= 2006 |pmid= 16273094 |doi= 10.1038/ncb1335
*cite journal | author=Monferrer L, Artero R |title=An interspecific functional complementation test in Drosophila for introductory genetics laboratory courses. |journal=J. Hered. |volume=97 |issue= 1 |pages= 67–73 |year= 2006 |pmid= 16394256 |doi= 10.1093/jhered/esj003
*cite journal | author=Cardani R, Mancinelli E, Rotondo G, "et al." |title=Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2. |journal=European journal of histochemistry : EJH |volume=50 |issue= 3 |pages= 177–82 |year= 2007 |pmid= 16920640 |doi=
*cite journal | author=Paul S, Dansithong W, Kim D, "et al." |title=Interaction of muscleblind, CUG-BP1 and hnRNP H proteins in DM1-associated aberrant IR splicing. |journal=EMBO J. |volume=25 |issue= 18 |pages= 4271–83 |year= 2006 |pmid= 16946708 |doi= 10.1038/sj.emboj.7601296
*cite journal | author=Smith KP, Byron M, Johnson C, "et al." |title=Defining early steps in mRNA transport: mutant mRNA in myotonic dystrophy type I is blocked at entry into SC-35 domains. |journal=J. Cell Biol. |volume=178 |issue= 6 |pages= 951–64 |year= 2007 |pmid= 17846170 |doi= 10.1083/jcb.200706048

PBB_Controls
update_page = yes
require_manual_inspection = no
update_protein_box = yes
update_summary = yes
update_citations = yes


Wikimedia Foundation. 2010.

Игры ⚽ Нужно сделать НИР?

Look at other dictionaries:

  • Trinucleotide repeat disorder — Trinucleotide repeat disorders (also known as trinucleotide repeat expansion disorders, triplet repeat expansion disorders or codon reiteration disorders) are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation …   Wikipedia

  • CUGBP1 — CUG triplet repeat, RNA binding protein 1, also known as CUGBP1, is a human gene.cite web | title = Entrez Gene: CUGBP1 CUG triplet repeat, RNA binding protein 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”