Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer.

scientific article

Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer. is …
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scholarly articleQ13442814

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P356DOI10.1007/S00439-002-0892-2
P698PubMed publication ID12545275

P50authorDavid N. CooperQ30503192
Leslie G BieseckerQ65054829
Clesson E TurnerQ89916173
P2093author name stringJennifer Johnston
Christina Killoran
Nadia A Chuzhanova
Marjorie Rosenberg
Nick S T Thomas
Yelena Kemel
P2860cites workHuman minisatellite mutation rate after the Chernobyl accidentQ22337273
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Pattern of organization of human mitochondrial pseudogenes in the nuclear genomeQ28768380
Mitochondrial DNA migration events in yeast and humans: integration by a common end-joining mechanism and alternative perspectives on nucleotide substitution patternsQ29306611
Pallister-Hall syndromeQ33677551
Ionizing radiation and genetic risks. X. The potential "disease phenotypes" of radiation-induced genetic damage in humans: perspectives from human molecular biology and radiation geneticsQ33703747
Structure and chromosomal distribution of human mitochondrial pseudogenesQ33959798
X-ray induced DNA double-strand breaks in human spermQ34459215
New evidence for the insertion of mitochondrial DNA into the human genome: significance for cancer and agingQ35341049
Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutationsQ36833616
How do mitochondrial genes get into the nucleus?Q38577569
Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesisQ38915020
Radiation-induced genomic rearrangements formed by nonhomologous end-joining of DNA double-strand breaksQ40805209
Escape and migration of nucleic acids between chloroplasts, mitochondria, and the nucleusQ41195823
RET rearrangements in radiation-induced papillary thyroid carcinomas: high prevalence of topoisomerase I sites at breakpoints and microhomology-mediated end joining in ELE1 and RET chimeric genesQ43585900
The evaluation of the germinal mutagenic impact of Chernobyl radiological contamination in HungaryQ44610343
Novel mitochondrial DNA insertion polymorphism and its usefulness for human population studies.Q47814777
Human Gene Mutation Database (HGMD): 2003 updateQ47903166
On the complexity measures of genetic sequences.Q52080291
Gene structure and allelic expression assay of the human GLI3 gene.Q52191817
GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndromeQ55670535
Transgenerational mutation by radiationQ59068054
The Human Genome Project Reveals a Continuous Transfer of Large Mitochondrial Fragments to the NucleusQ60297610
Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocationQ64388078
Chromosomal breakpoint positions suggest a direct role for radiation in inducing illegitimate recombination between the ELE1 and RET genes in radiation-induced thyroid carcinomasQ73270725
[The Pallister-Hall syndrome--a rare case and an example of the differentiated approach to the treatment of hormonally inactive hypothalamic hamartomas]Q73334545
Further evidence for elevated human minisatellite mutation rate in Belarus eight years after the Chernobyl accidentQ74063643
RET/PTC rearrangements in thyroid nodules: studies in irradiated and not irradiated, malignant and benign thyroid lesions in children and adultsQ74154750
Hungarian surveillance of germinal mutations. Lack of detectable increase in indicator conditions caused by germinal mutations following the Chernobyl accidentQ93512191
P433issue3
P921main subjectgenetic diseaseQ200779
P304page(s)303-309
P577publication date2003-01-25
P1433published inHuman GeneticsQ5937167
P1476titleHuman genetic disease caused by de novo mitochondrial-nuclear DNA transfer.
P478volume112

Reverse relations

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