An intron 9 containing splice variant of PAX2

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1479-5876

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: An intron 9 containing splice variant of PAX2 ; volume:7 ; number:1 ; day:25 ; month:5 ; year:2009 ; pages:1-6 ; date:12.2009
Journal of translational medicine ; 7, Heft 1 (25.5.2009), 1-6, 12.2009

Creator: Busse, Antonia

Contributor: Rietz, Anika
Schwartz, Stefan
Thiel, Eckhard
Keilholz, Ulrich
SpringerLink (Online service)

DOI: 10.1186/1479-5876-7-36

URN: urn:nbn:de:1111-2016041433674

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 11:00 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Busse, Antonia
Rietz, Anika
Schwartz, Stefan
Thiel, Eckhard
Keilholz, Ulrich
SpringerLink (Online service)

Other Objects (12)

Hochschulschrift

Identifikation of the novel PDZ domain containing splice variant GRIP1k-a potential interaction partner of prominin-2

SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation

CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores

Mapping intron retention events contributing to complex traits using splice quantitative trait locus

Characterisation of a novel OPA1 splice variant resulting in cryptic splice site activation and mitochondrial dysfunction

Analysis of CCR2 splice variant expression patterns and functional properties

Reversible mislocalization of a disease-associated MRE11 splice variant product

SpliceMiner: a high-throughput database implementation of the NCBI Evidence Viewer for microarray splice variant analysis

Novel splice site variant of TMEM38B in osteogenesis imperfecta type XIV

The landscape of d16HER2 splice variant expression across HER2-positive cancers

Benchmarking splice variant prediction algorithms using massively parallel splicing assays

Duchenne muscular dystrophy caused by a frame-shift mutation in the acceptor splice site of intron 26

Hochschulschrift

Identifikation of the novel PDZ domain containing splice variant GRIP1k-a potential interaction partner of prominin-2

SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation

CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores

Mapping intron retention events contributing to complex traits using splice quantitative trait locus

Characterisation of a novel OPA1 splice variant resulting in cryptic splice site activation and mitochondrial dysfunction

Analysis of CCR2 splice variant expression patterns and functional properties

Reversible mislocalization of a disease-associated MRE11 splice variant product

SpliceMiner: a high-throughput database implementation of the NCBI Evidence Viewer for microarray splice variant analysis

Novel splice site variant of TMEM38B in osteogenesis imperfecta type XIV

The landscape of d16HER2 splice variant expression across HER2-positive cancers

Benchmarking splice variant prediction algorithms using massively parallel splicing assays

Duchenne muscular dystrophy caused by a frame-shift mutation in the acceptor splice site of intron 26

Hochschulschrift

Identifikation of the novel PDZ domain containing splice variant GRIP1k-a potential interaction partner of prominin-2

SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation

CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores

Mapping intron retention events contributing to complex traits using splice quantitative trait locus

Characterisation of a novel OPA1 splice variant resulting in cryptic splice site activation and mitochondrial dysfunction

Analysis of CCR2 splice variant expression patterns and functional properties

Reversible mislocalization of a disease-associated MRE11 splice variant product

SpliceMiner: a high-throughput database implementation of the NCBI Evidence Viewer for microarray splice variant analysis

Novel splice site variant of TMEM38B in osteogenesis imperfecta type XIV

The landscape of d16HER2 splice variant expression across HER2-positive cancers

Benchmarking splice variant prediction algorithms using massively parallel splicing assays

Duchenne muscular dystrophy caused by a frame-shift mutation in the acceptor splice site of intron 26

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

An intron 9 containing splice variant of PAX2

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Identifikation of the novel PDZ domain containing splice variant GRIP1k-a potential interaction partner of prominin-2

SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation

CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores

Mapping intron retention events contributing to complex traits using splice quantitative trait locus

Characterisation of a novel OPA1 splice variant resulting in cryptic splice site activation and mitochondrial dysfunction

Analysis of CCR2 splice variant expression patterns and functional properties

Reversible mislocalization of a disease-associated MRE11 splice variant product

SpliceMiner: a high-throughput database implementation of the NCBI Evidence Viewer for microarray splice variant analysis

Novel splice site variant of TMEM38B in osteogenesis imperfecta type XIV

The landscape of d16HER2 splice variant expression across HER2-positive cancers

Benchmarking splice variant prediction algorithms using massively parallel splicing assays

Duchenne muscular dystrophy caused by a frame-shift mutation in the acceptor splice site of intron 26

Identifikation of the novel PDZ domain containing splice variant GRIP1k-a potential interaction partner of prominin-2

SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation

CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores

Mapping intron retention events contributing to complex traits using splice quantitative trait locus

Characterisation of a novel OPA1 splice variant resulting in cryptic splice site activation and mitochondrial dysfunction

Analysis of CCR2 splice variant expression patterns and functional properties

Reversible mislocalization of a disease-associated MRE11 splice variant product

SpliceMiner: a high-throughput database implementation of the NCBI Evidence Viewer for microarray splice variant analysis

Novel splice site variant of TMEM38B in osteogenesis imperfecta type XIV

The landscape of d16HER2 splice variant expression across HER2-positive cancers

Benchmarking splice variant prediction algorithms using massively parallel splicing assays

Duchenne muscular dystrophy caused by a frame-shift mutation in the acceptor splice site of intron 26

Identifikation of the novel PDZ domain containing splice variant GRIP1k-a potential interaction partner of prominin-2

SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation

CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores

Mapping intron retention events contributing to complex traits using splice quantitative trait locus

Characterisation of a novel OPA1 splice variant resulting in cryptic splice site activation and mitochondrial dysfunction

Analysis of CCR2 splice variant expression patterns and functional properties

Reversible mislocalization of a disease-associated MRE11 splice variant product

SpliceMiner: a high-throughput database implementation of the NCBI Evidence Viewer for microarray splice variant analysis

Novel splice site variant of TMEM38B in osteogenesis imperfecta type XIV

The landscape of d16HER2 splice variant expression across HER2-positive cancers

Benchmarking splice variant prediction algorithms using massively parallel splicing assays

Duchenne muscular dystrophy caused by a frame-shift mutation in the acceptor splice site of intron 26

Related objects

Reset password