Role of chimeric transcript formation in the pathogenesis of birth defects-Reference-Cited by-同舟云学术

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Role of chimeric transcript formation in the pathogenesis of birth defects

Published:2020-11-24 Issue:3 Volume:61 Page:76-81
ISSN:0914-3505
Container-title:Congenital Anomalies
language:en
Short-container-title:Congenit Anom

Author:

Yamada Mamiko¹^ORCID,Suzuki Hisato¹,Watanabe Akiko²,Uehara Tomoko¹³,Takenouchi Toshiki⁴,Mizuno Seiji³^ORCID,Kosaki Kenjiro¹^ORCID

Affiliation:

1. Center for Medical Genetics Keio University School of Medicine Tokyo Japan

2. Department of Pediatrics Juntendo University Urayasu Hospital Chiba Japan

3. Department of Pediatrics, Central Hospital Aichi Developmental Disability Center Aichi Japan

4. Department of Pediatrics Keio University School of Medicine Tokyo Japan

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cga.12400

Reference17 articles.

1. Fusion genes and chromosome translocations in the common epithelial cancers

2. Ewing’s sarcoma

3. A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia

4. A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia identified by Quinacrine Fluorescence and Giemsa Staining

5. Reanalysis of RNA-Sequencing Data Reveals Several Additional Fusion Genes with Multiple Isoforms

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2. A germline chimeric KANK1-DMRT1 transcript derived from a complex structural variant is associated with a congenital heart defect segregating across five generations;Chromosome Research;2024-03-19

3. Successful skipping of abnormal pseudoexon by antisense oligonucleotides in vitro for a patient with beta-propeller protein-associated neurodegeneration;Scientific Reports;2024-03-18

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