ORIGINAL RESEARCH
Published on 13 May 2022
Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression
doi 10.3389/fgene.2022.867989
- 1,763 views
- 2 citations
- Frontiers in Genetics
- Genetics of Common and Rare Diseases
- Research Topics
- Gene expression, Molecular Pathways and Organelle Alterations in Down syndrome Phenotype.
Gene expression, Molecular Pathways and Organelle Alterations in Down syndrome Phenotype.
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Articles
ORIGINAL RESEARCH
Published on 27 Apr 2022
DNA Methylation Analysis of Ribosomal DNA in Adults With Down Syndrome
doi 10.3389/fgene.2022.792165
- 2,545 views
- 12 citations
ORIGINAL RESEARCH
Published on 10 Mar 2022
Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells
doi 10.3389/fgene.2022.824922
- 2,646 views
- 7 citations
REVIEW
Published on 18 Jan 2022
New Molecular and Organelle Alterations Linked to Down Syndrome Heart Disease
doi 10.3389/fgene.2021.792231
- 5,045 views
- 12 citations
ORIGINAL RESEARCH
Published on 08 Dec 2021
Structural Characterization of the Highly Restricted Down Syndrome Critical Region on 21q22.13: New KCNJ6 and DSCR4 Transcript Isoforms
doi 10.3389/fgene.2021.770359
- 3,355 views
- 11 citations
REVIEW
Published on 05 Nov 2021
Ten Reasons Why People With Down Syndrome are Protected From the Development of Most Solid Tumors -A Review
doi 10.3389/fgene.2021.749480
- 15,006 views
- 21 citations
Published in
Frontiers in Genetics
Genetics of Common and Rare Diseases
Participating Journals
Frontiers in Pediatrics
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- 3.6 citescore