Fmr1 exon 14 skipping in late embryonic development of the rat forebrain

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2202

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Fmr1 exon 14 skipping in late embryonic development of the rat forebrain ; volume:23 ; number:1 ; day:31 ; month:5 ; year:2022 ; pages:1-15 ; date:12.2022
BMC neuroscience ; 23, Heft 1 (31.5.2022), 1-15, 12.2022

Creator: Corrêa-Velloso, Juliana C.
Linardi, Alessandra M.
Glaser, Talita
Velloso, Fernando J.
Rivas, Maria P.
Leite, Renata E P.
Grinberg, Lea T.
Ulrich, Henning
Akins, Michael R.
Chiavegatto, Silvana
Haddad, Luciana Amaral

Contributor: SpringerLink (Online service)

DOI: 10.1186/s12868-022-00711-1

URN: urn:nbn:de:101:1-2022073107480171918752

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:30 AM CEST

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Associated

Corrêa-Velloso, Juliana C.
Linardi, Alessandra M.
Glaser, Talita
Velloso, Fernando J.
Rivas, Maria P.
Leite, Renata E P.
Grinberg, Lea T.
Ulrich, Henning
Akins, Michael R.
Chiavegatto, Silvana
Haddad, Luciana Amaral
SpringerLink (Online service)

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Fmr1 exon 14 skipping in late embryonic development of the rat forebrain

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Other Objects (12)

Exon skipping for DMD

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

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Unexpected consequences: exon skipping caused by CRISPR-generated mutations

CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion

A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data

Antisense-induced exon skipping for duplications in Duchenne muscular dystrophy

Exon skipping-rich transcriptomes of animals reflect the significance of exon-shuffling in metazoan proteome evolution

CRISPR-induced exon skipping is dependent on premature termination codon mutations

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy

SRSF10 stabilizes CDC25A by triggering exon 6 skipping to promote hepatocarcinogenesis

Exon skipping for DMD

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Exon skipping as a therapeutic strategy in dysferlinopathy

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Unexpected consequences: exon skipping caused by CRISPR-generated mutations

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A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data

Antisense-induced exon skipping for duplications in Duchenne muscular dystrophy

Exon skipping-rich transcriptomes of animals reflect the significance of exon-shuffling in metazoan proteome evolution

CRISPR-induced exon skipping is dependent on premature termination codon mutations

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy

SRSF10 stabilizes CDC25A by triggering exon 6 skipping to promote hepatocarcinogenesis

Exon skipping for DMD

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

Applying Lessons Learned from Developing Exon Skipping for Duchenne to Developing Individualized Exon Skipping Therapy for Patients with Neurodegenerative Diseases

Unexpected consequences: exon skipping caused by CRISPR-generated mutations

CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion

A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data

Antisense-induced exon skipping for duplications in Duchenne muscular dystrophy

Exon skipping-rich transcriptomes of animals reflect the significance of exon-shuffling in metazoan proteome evolution

CRISPR-induced exon skipping is dependent on premature termination codon mutations

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy

SRSF10 stabilizes CDC25A by triggering exon 6 skipping to promote hepatocarcinogenesis

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