- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1476-4598
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Dynamics of double strand breaks and chromosomal translocations ; volume:13 ; number:1 ; day:18 ; month:11 ; year:2014 ; pages:1-10 ; date:12.2014
Molecular cancer ; 13, Heft 1 (18.11.2014), 1-10, 12.2014
- Urheber
-
Iarovaia, Olga V.
Rubtsov, Mikhail
Ioudinkova, Elena
Tsfasman, Tatiana
Razin, Sergey V.
Vassetzky, Yegor S.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/1476-4598-13-249
- URN
-
urn:nbn:de:101:1-2021082219340769364827
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:55 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Iarovaia, Olga V.
- Rubtsov, Mikhail
- Ioudinkova, Elena
- Tsfasman, Tatiana
- Razin, Sergey V.
- Vassetzky, Yegor S.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations
Chromosomal translocations and oncogenic transcription factors
The molecular principles of chromosomal translocations
The spectrum of chromosomal translocations in the Arab world: ethnic-specific chromosomal translocations and their relevance to diseases
Do non-genomically encoded fusion transcripts cause recurrent chromosomal translocations?
DNA double strand breaks in hypermutating Ig genes
DNA double strand breaks : formation, repair and consequences
DNA double-strand break signaling and human disorders
Radiation Induced DNA Double-Strand Breaks in Radiology
Impact of single strand annealing on double strand break repair and chromosomal stability in mammalian cells : a component of the repair network
Efficient generation and reversion of chromosomal translocations using CRISPR/Cas technology
Tyrosine kinase chromosomal translocations mediate distinct and overlapping gene regulation events
Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations
Chromosomal translocations and oncogenic transcription factors
The molecular principles of chromosomal translocations
The spectrum of chromosomal translocations in the Arab world: ethnic-specific chromosomal translocations and their relevance to diseases
Do non-genomically encoded fusion transcripts cause recurrent chromosomal translocations?
DNA double strand breaks in hypermutating Ig genes
DNA double strand breaks : formation, repair and consequences
DNA double-strand break signaling and human disorders
Radiation Induced DNA Double-Strand Breaks in Radiology
Impact of single strand annealing on double strand break repair and chromosomal stability in mammalian cells : a component of the repair network
Efficient generation and reversion of chromosomal translocations using CRISPR/Cas technology
Tyrosine kinase chromosomal translocations mediate distinct and overlapping gene regulation events
Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations
Chromosomal translocations and oncogenic transcription factors
The molecular principles of chromosomal translocations
The spectrum of chromosomal translocations in the Arab world: ethnic-specific chromosomal translocations and their relevance to diseases
Do non-genomically encoded fusion transcripts cause recurrent chromosomal translocations?
DNA double strand breaks in hypermutating Ig genes
DNA double strand breaks : formation, repair and consequences
DNA double-strand break signaling and human disorders
Radiation Induced DNA Double-Strand Breaks in Radiology
Impact of single strand annealing on double strand break repair and chromosomal stability in mammalian cells : a component of the repair network
Efficient generation and reversion of chromosomal translocations using CRISPR/Cas technology