The First Korean Case of SLC12A3 Aberrant Skipping of Two Exons Detected by RNA Splicing Analysis

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: The First Korean Case of SLC12A3 Aberrant Skipping of Two Exons Detected by RNA Splicing Analysis ; volume:11 ; number:2 ; year:2021 ; pages:210-213 ; extent:4
Case reports in nephrology and dialysis ; 11, Heft 2 (2021), 210-213 (gesamt 4)

Creator: Ko, Kiwoong
Kim, Jong-Won

DOI: 10.1159/000517139

URN: urn:nbn:de:101:1-2021091600425981648973

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

Last update: 15.08.2025, 7:35 AM CEST

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Ko, Kiwoong
Kim, Jong-Won

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Elevated nuclear TDP-43 induces constitutive exon skipping

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The First Korean Case of SLC12A3 Aberrant Skipping of Two Exons Detected by RNA Splicing Analysis

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Other Objects (12)

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

Reverse complementary matches simultaneously promote both back-splicing and exon-skipping

Exon skipping for DMD

Deciphering Splicing Regulation for TRAF3 Exon 8 Alternative Splicing – CELF2 and hnRNP C Regulate TRAF3 Exon 8 Skipping Upon T Cell Activation

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

Aberrant single exon skipping is not altered by age in exons of NF1, RABAC1, AATF or PCGF2 in human blood cells and fibroblasts

Global analysis of aberrant pre-mRNA splicing in glioblastoma using exon expression arrays

A Novel COL4A5 Splicing Mutation Causes Skipping of Exon 14 in a Chinese Family with Alport Syndrome

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

Multiple tandem splicing silencer elements suppress aberrant splicing within the long exon 26 of the human Apolipoprotein B gene

CRISPR/Cas9-mediated genome editing induces exon skipping by complete or stochastic altering splicing in the migratory locust

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

Reverse complementary matches simultaneously promote both back-splicing and exon-skipping

Exon skipping for DMD

Deciphering Splicing Regulation for TRAF3 Exon 8 Alternative Splicing – CELF2 and hnRNP C Regulate TRAF3 Exon 8 Skipping Upon T Cell Activation

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

Aberrant single exon skipping is not altered by age in exons of NF1, RABAC1, AATF or PCGF2 in human blood cells and fibroblasts

Global analysis of aberrant pre-mRNA splicing in glioblastoma using exon expression arrays

A Novel COL4A5 Splicing Mutation Causes Skipping of Exon 14 in a Chinese Family with Alport Syndrome

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

Multiple tandem splicing silencer elements suppress aberrant splicing within the long exon 26 of the human Apolipoprotein B gene

CRISPR/Cas9-mediated genome editing induces exon skipping by complete or stochastic altering splicing in the migratory locust

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

Reverse complementary matches simultaneously promote both back-splicing and exon-skipping

Exon skipping for DMD

Deciphering Splicing Regulation for TRAF3 Exon 8 Alternative Splicing – CELF2 and hnRNP C Regulate TRAF3 Exon 8 Skipping Upon T Cell Activation

Elevated nuclear TDP-43 induces constitutive exon skipping

Exon skipping as a therapeutic strategy in dysferlinopathy

Aberrant single exon skipping is not altered by age in exons of NF1, RABAC1, AATF or PCGF2 in human blood cells and fibroblasts

Global analysis of aberrant pre-mRNA splicing in glioblastoma using exon expression arrays

A Novel COL4A5 Splicing Mutation Causes Skipping of Exon 14 in a Chinese Family with Alport Syndrome

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

Multiple tandem splicing silencer elements suppress aberrant splicing within the long exon 26 of the human Apolipoprotein B gene

CRISPR/Cas9-mediated genome editing induces exon skipping by complete or stochastic altering splicing in the migratory locust

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