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Deletion Mutation

Known as: Deletion Abnormality, Mutations, Deletion, Deletion Mutations 
Any rearrangement to the genomic content that results in the loss of one or more nucleotides of DNA. Deletions are generally irreversible… Expand
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Inherited loss-of-function mutations in the tumor suppressor genes BRCA1, BRCA2, and multiple other genes predispose to high… Expand
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Highly Cited
2006
Highly Cited
2006
Skeletal muscle-mass loss with age has severe health consequences, yet the molecular basis of the loss remains obscure. Although… Expand
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Highly Cited
2005
Highly Cited
2005
The endoplasmic reticulum (ER) transmits apoptotic signals in the pancreas during ER stress, implicating ER stress-mediated… Expand
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Highly Cited
2002
Highly Cited
2002
The p53 tumour suppressor is activated by numerous stressors to induce apoptosis, cell cycle arrest, or senescence. To study the… Expand
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Highly Cited
2001
Highly Cited
2001
A subpopulation of collie dogs is extremely sensitive to neurotoxicity induced by ivermectin. The aim of this study was to… Expand
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Highly Cited
2001
Highly Cited
2001
The in vivo cellular impact of age-associated mitochondrial DNA mutations is unknown. We hypothesized that mitochondrial DNA… Expand
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Highly Cited
2000
Highly Cited
2000
Congenital cataracts are a common major abnormality of the eye that frequently cause blindness in infants. At least one-third of… Expand
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Highly Cited
1996
Highly Cited
1996
Mouse Otx2 is a bicoid-class homeobox gene, related to the Drosophila orthodenticle (otd) gene. Expression of this gene is… Expand
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Highly Cited
1995
Highly Cited
1995
Two cassettes with tetracycline-resistance (TcR) and kanamycin-resistance (KmR) determinants have been developed for the… Expand
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Highly Cited
1987
Highly Cited
1987
The 14 kb human Duchenne muscular dystrophy (DMD) cDNA corresponding to a complete representation of the fetal skeletal muscle… Expand
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