(Q28300006)

1

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J Kaukonen

2

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P Amati

3

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R Timonen

4

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M Haltia

5

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M Zeviani

7

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H Somer

8

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L Peltonen

RTG1 and RTG2: two yeast genes required for a novel path of communication from mitochondria to the nucleus

9

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language of work or name

English

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publication date

February 1995

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published in

Nature Genetics

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volume

9

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issue

2

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page(s)

146-51

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cites work

1 reference

The 1993-94 Généthon human genetic linkage map

21 April 2017

1 reference

An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21

21 April 2017

1 reference

Upstream region of a genomic gene for human mitochondrial transcription factor 1

21 April 2017

1 reference

Diseases of the mitochondrial DNA.

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

Nuclear gadgets in mitochondrial DNA replication and transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

Toward a physical map of human chromosome 10: isolation of 183 YACs representing 80 loci and regional assignment of 94 YACs by fluorescence in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

Development of 124 sequence-tagged sites and cytogenetic localization of 217 cosmids for human chromosome 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

Activation of the human mitochondrial transcription factor A gene by nuclear respiratory factors: a potential regulatory link between nuclear and mitochondrial gene expression in organelle biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Marked decrease of mitochondrial DNA with multiple deletions in a patient with familial mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Mitochondrial DNA deletions in inherited recurrent myoglobinuria

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Computer-simulation methods in human linkage analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Nucleus-driven mutations of human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Mitochondrial DNA deletions in inclusion body myositis

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Detection of a specific mitochondrial DNA deletion in tissues of older humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Quantification of tRNA3243(Leu) point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcription

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021

Direct sequencing of affinity-captured amplified human DNA application to the detection of apolipoprotein E polymorphism

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-146

7 January 2021