Lack of the DNA glycosylases MYH and OGG1 in the cancer prone double mutant mouse does not increase mitochondrial DNA mutagenesis

Ruth Halsne; Ying Esbensen; Wei Wang; Katja Scheffler; Rajikala Suganthan; Magnar Bjørås; Lars Eide

doi:10.1016/j.dnarep.2011.12.001

Lack of the DNA glycosylases MYH and OGG1 in the cancer prone double mutant mouse does not increase mitochondrial DNA mutagenesis

DNA Repair ◽

10.1016/j.dnarep.2011.12.001 ◽

2012 ◽

Vol 11 (3) ◽

pp. 278-285 ◽

Cited By ~ 29

Author(s):

Ruth Halsne ◽

Ying Esbensen ◽

Wei Wang ◽

Katja Scheffler ◽

Rajikala Suganthan ◽

...

Keyword(s):

Mitochondrial Dna ◽

Double Mutant ◽

Mutant Mouse ◽

Dna Glycosylases ◽

Double Mutant Mouse ◽

Dna Mutagenesis

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Losartan Improves Survival and Cardiac Function in a Double-mutant Mouse Model of Severe Hypertrophic Cardiomyopathy

Heart Lung and Circulation ◽

10.1016/j.hlc.2011.05.020 ◽

2011 ◽

Vol 20 ◽

pp. S8

Author(s):

R. Shephard ◽

T. Tsoutsman ◽

C. Semsarian

Keyword(s):

Hypertrophic Cardiomyopathy ◽

Mouse Model ◽

Cardiac Function ◽

Double Mutant ◽

Mutant Mouse ◽

Double Mutant Mouse

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Rad51c- and Trp53-double-mutant mouse model reveals common features of homologous recombination-deficient breast cancers

Oncogene ◽

10.1038/onc.2015.528 ◽

2016 ◽

Vol 35 (35) ◽

pp. 4601-4610 ◽

Cited By ~ 2

Author(s):

M Tumiati ◽

P M Munne ◽

H Edgren ◽

S Eldfors ◽

A Hemmes ◽

...

Keyword(s):

Homologous Recombination ◽

Mouse Model ◽

Double Mutant ◽

Mutant Mouse ◽

Breast Cancers ◽

Common Features ◽

Double Mutant Mouse

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Effects of carbonic anhydrase II (CAII) deficiency on CNS structure and function in the myelin-deficient CAII-deficient double mutant mouse

Journal of Neuroscience Research ◽

10.1002/jnr.490400404 ◽

1995 ◽

Vol 40 (4) ◽

pp. 451-457 ◽

Cited By ~ 18

Author(s):

Wendy Cammer ◽

H. Zhang ◽

F. A. Tansey

Keyword(s):

Carbonic Anhydrase ◽

Double Mutant ◽

Mutant Mouse ◽

Structure And Function ◽

Carbonic Anhydrase Ii ◽

And Function ◽

Myelin Deficient ◽

Double Mutant Mouse

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P3.24 Therapeutic potential of murine mesenchymal stem cells (MSC) from adipose tissue in the treatment of muscular dystrophy in the new double mutant mouse model for the genes Dystrophin and Large

Neuromuscular Disorders ◽

10.1016/j.nmd.2010.07.166 ◽

2010 ◽

Vol 20 (9-10) ◽

pp. 648

Author(s):

P.C.M. Martins-Machado ◽

P.C.G. Onofre-Oliveira ◽

D. Ayub-Guerrieri ◽

D. Gotlieb ◽

A. Fernandes ◽

...

Keyword(s):

Stem Cells ◽

Mesenchymal Stem Cells ◽

Adipose Tissue ◽

Muscular Dystrophy ◽

Mouse Model ◽

Double Mutant ◽

Mutant Mouse ◽

Therapeutic Potential ◽

Double Mutant Mouse

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Improvement in survival and muscle function in an mdx/utrn−/− double mutant mouse using a human retinal dystrophin transgene

Neuromuscular Disorders ◽

10.1016/j.nmd.2005.12.007 ◽

2006 ◽

Vol 16 (3) ◽

pp. 192-203 ◽

Cited By ~ 8

Author(s):

Roger Gaedigk ◽

Douglas J. Law ◽

Kathleen M. Fitzgerald-Gustafson ◽

Steven G. McNulty ◽

Ndona N. Nsumu ◽

...

Keyword(s):

Muscle Function ◽

Double Mutant ◽

Mutant Mouse ◽

Improvement In Survival ◽

Double Mutant Mouse

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G.P.8.03 Generation of double mutant mouse for the genes dystrophin and large: A new model for neuromuscular diseases

Neuromuscular Disorders ◽

10.1016/j.nmd.2008.06.202 ◽

2008 ◽

Vol 18 (9-10) ◽

pp. 782

Author(s):

P.C.M. Martins ◽

D. Ayub-Guerrieri ◽

V.F. Lopes ◽

P.C.G. Onofre ◽

C.M.C. Mori ◽

...

Keyword(s):

Double Mutant ◽

Mutant Mouse ◽

Neuromuscular Diseases ◽

New Model ◽

Double Mutant Mouse

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Mono- and double-mutant mouse models of Parkinson's disease display severe mitochondrial damage

Human Molecular Genetics ◽

10.1093/hmg/ddm083 ◽

2007 ◽

Vol 16 (20) ◽

pp. 2377-2393 ◽

Cited By ~ 116

Author(s):

C. C. Stichel ◽

X.-R. Zhu ◽

V. Bader ◽

B. Linnartz ◽

S. Schmidt ◽

...

Keyword(s):

Parkinson’S Disease ◽

Parkinson's Disease ◽

Mouse Models ◽

Double Mutant ◽

Mutant Mouse ◽

Mitochondrial Damage ◽

Double Mutant Mouse

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Functional analysis in vivo of the double mutant mouse deficient in both proteolipid protein (PLP) and myelin basic protein (MBP) in the central nervous system

Cell and Tissue Research ◽

10.1007/s004410050866 ◽

1997 ◽

Vol 289 (2) ◽

pp. 195-206 ◽

Cited By ~ 14

Author(s):

Wilhelm Stoffel ◽

Detlev Boison ◽

Heinrich Büssow

Keyword(s):

Central Nervous System ◽

Functional Analysis ◽

Nervous System ◽

Double Mutant ◽

Basic Protein ◽

Mutant Mouse ◽

Proteolipid Protein ◽

The Central Nervous System ◽

Double Mutant Mouse

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Corrigendum to “Genetic and Diet-Induced Obesity Increased Intestinal Tumorigenesis in the Double Mutant Mouse Model Multiple Intestinal Neoplasia X Obese via Disturbed Glucose Regulation and Inflammation”

Journal of Obesity ◽

10.1155/2016/2361290 ◽

2016 ◽

Vol 2016 ◽

pp. 1-2

Author(s):

Ha Thi Ngo ◽

Ragna Bogen Hetland ◽

Unni Cecilie Nygaard ◽

Inger-Lise Steffensen

Keyword(s):

Mouse Model ◽

Double Mutant ◽

Mutant Mouse ◽

Glucose Regulation ◽

Intestinal Tumorigenesis ◽

Diet Induced Obesity ◽

Intestinal Neoplasia ◽

Double Mutant Mouse

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Hereditary Defect of the Pilosebaceous Unit in a New Double Mutant Mouse**From the Department of Gynecology and Obstetrics and the Department of Dermatology, Stanford University School of Medicine, Stanford, California 94305.

Journal of Investigative Dermatology ◽

10.1038/jid.1969.18 ◽

1969 ◽

Vol 52 (2) ◽

pp. 115-118 ◽

Cited By ~ 16

Author(s):

Allen H. Gates ◽

Faye D. Arundell ◽

Marvin A. Karasek

Keyword(s):

Double Mutant ◽

Mutant Mouse ◽

Stanford University ◽

Pilosebaceous Unit ◽

School Of Medicine ◽

Gynecology And Obstetrics ◽

Hereditary Defect ◽

Double Mutant Mouse

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