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Search results 301 to 315 out of 315 for Six5

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Genotype

Symbol:	Tg(DMWD,DMPK,SIX5)1177Ggo/Tg(DMWD,DMPK,SIX5)1177Ggo
Background:	involves: C57BL/6 * DBA/2
Zygosity:	hm
Has Mutant Allele:	true

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Genotype

Symbol:	Tg(DMWD,DMPK,SIX5)328Ggo/Tg(DMWD,DMPK,SIX5)328Ggo
Background:	involves: 129 * C57BL/6 * DBA/2 * FVB/N
Zygosity:	hm
Has Mutant Allele:	true

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Publication

15788460 | J:98519

First Author:	Grifone R
Year:	2005
Journal:	Development
Title:	Six1 and Six4 homeoproteins are required for Pax3 and Mrf expression during myogenesis in the mouse embryo.
Volume:	132
Issue:	9
Pages:	2235-49

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Publication

12727892 | J:83373

First Author:	Savouret C
Year:	2003
Journal:	EMBO J
Title:	CTG repeat instability and size variation timing in DNA repair-deficient mice.
Volume:	22
Issue:	9
Pages:	2264-73

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Publication

21378394 | J:171506

First Author:	Tomé S
Year:	2011
Journal:	Hum Mol Genet
Title:	Maternal germline-specific effect of DNA ligase I on CTG/CAG instability.
Volume:	20
Issue:	11
Pages:	2131-43

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Publication

28658620 | J:254355

First Author:	Sicot G
Year:	2017
Journal:	Cell Rep
Title:	Downregulation of the Glial GLT1 Glutamate Transporter and Purkinje Cell Dysfunction in a Mouse Model of Myotonic Dystrophy.
Volume:	19
Issue:	13
Pages:	2718-2729

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Publication

19436705 | J:149536

First Author:	Tomé S
Year:	2009
Journal:	PLoS Genet
Title:	MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice.
Volume:	5
Issue:	5
Pages:	e1000482

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Publication

26908607 | J:231444

First Author:	Gudde AE
Year:	2016
Journal:	Hum Mol Genet
Title:	A low absolute number of expanded transcripts is involved in myotonic dystrophy type 1 manifestation in muscle.
Volume:	25
Issue:	8
Pages:	1648-62

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Publication

10767343 | J:168896

First Author:	Seznec H
Year:	2000
Journal:	Hum Mol Genet
Title:	Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability.
Volume:	9
Issue:	8
Pages:	1185-94

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Publication

11726559 | J:73187

First Author:	Seznec H
Year:	2001
Journal:	Hum Mol Genet
Title:	Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.
Volume:	10
Issue:	23
Pages:	2717-26

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Publication

17098221 | J:119948

First Author:	Grifone R
Year:	2007
Journal:	Dev Biol
Title:	Eya1 and Eya2 proteins are required for hypaxial somitic myogenesis in the mouse embryo.
Volume:	302
Issue:	2
Pages:	602-16

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Publication

25799359 | J:229190

First Author:	González-Barriga A
Year:	2015
Journal:	PLoS One
Title:	Cell membrane integrity in myotonic dystrophy type 1: implications for therapy.
Volume:	10
Issue:	3
Pages:	e0121556

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Publication

37390204 | J:342764

First Author:	Da Silva A
Year:	2023
Journal:	Sci Adv
Title:	N-acetylneuraminate pyruvate lyase controls sialylation of muscle glycoproteins essential for muscle regeneration and function.
Volume:	9
Issue:	26
Pages:	eade6308

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Publication

33503262 | J:303720

First Author:	Tanner MK
Year:	2021
Journal:	Nucleic Acids Res
Title:	Targeted splice sequencing reveals RNA toxicity and therapeutic response in myotonic dystrophy.
Volume:	49
Issue:	4
Pages:	2240-2254

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Publication

19468303 | -

First Author:	Church DM
Year:	2009
Journal:	PLoS Biol
Title:	Lineage-specific biology revealed by a finished genome assembly of the mouse.
Volume:	7
Issue:	5
Pages:	e1000112

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