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Morpholino Publication Database
This database contains citations and abstracts for research using Morpholino oligos, as well as some review articles incorporating Morpholino data. You can search the content using the filter boxes below.
There are 12218 scientific papers returned from the database with the search filters currently being used below.
There are 12218 scientific papers returned from the database with the search filters currently being used below.
A Combination of Variants in SEPTIN9 and MSX1 Genes Leads to the Formation of Orofacial Clefts
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Citation:
Genes Cells. 2026 Jul;31(4):e70138. doi: 10.1111/gtc.70138. PMID: 42429105; PMCID: PMC13352469 Epub:
Not Epub Abstract:
Nonsyndromic cleft lip with or without palate (nCL/P) is a common congenital anomaly with a complex genetic basis. Previous... Delivery Method:
microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Uuganbayar U, Manojlovic Z, Ito N, Yamaguchi R, Ninomiya H, Shimada IS, Yamada C, Feigelson D, Schulz G, Auslander A, Rakotoarison S, Magee W 3rd, Hashimoto Y, Kato Y. A Combination of Variants in SEPTIN9 and MSX1 Genes Leads to the Formation of Orofacial Clefts. Genes Cells. 2026 Jul;31(4):e70138. doi: 10.1111/gtc.70138. PMID: 42429105; PMCID: PMC13352469. |
Splice-altering TP53 missense mutations as drivers of dysfunction and targets for RNA-based therapy
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Citation:
Stem Cell Res Ther. 2026 Jul 13. doi: 10.1186/s13287-026-05176-1. Epub ahead of print Epub:
Not Epub Abstract:
TP53 missense mutations introduce single amino acid substitutions in the p53 protein, which can lead to diverse functional... Organism or Cell Type:
TP53 knock-in cell models Citation Extract: Chung SK, Jung HB, Baek SJ, Park SM, Kim J, Lee SY, Min B, Kang YK. Splice-altering TP53 missense mutations as drivers of dysfunction and targets for RNA-based therapy. Stem Cell Res Ther. 2026 Jul 13. doi: 10.1186/s13287-026-05176-1. Epub ahead of print. |
Targeted α-synuclein mRNA degradation by PMO-based RNA-degrading chimeras
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Citation:
Proc Natl Acad Sci U S A. 2026 Jul 21;123(29):e2526461123. doi: 10.1073/pnas.2526461123. Epub 2026 Jul 14 Epub:
Not Epub Abstract:
α-Synucleinopathies are devastating neurodegenerative diseases characterized by pathological accumulation of a neuronal protein... Delivery Method:
PMO-based RNA-degrading chimeras; motor cortex infusion for mice Organism or Cell Type:
cell culture: HEK293T cells, primary cortical neurons from humanized SNCA mice and human IPSC–derived cortical neurons; humanized SNCA mice Citation Extract: Wang N, Hegde S, Tang Z, Liu H, Feng G, Niu L, Liu B, Li H, Zhang X, Gadhave K, Kumbhar R, Jiang L, Liu Y, Luo M, Zhang S, Dawson TM, Pantelyat A, Rosenthal LS, Ying M, Mao X, Wang J
. Targeted α-synuclein mRNA degradation by PMO-based RNA-degrading chimeras. Proc Natl Acad Sci U S A. 2026 Jul 21;123(29):e2526461123. doi: 10.1073/pnas.2526461123. Epub 2026 Jul 14. |
Oxidized PDI promotes thrombus formation in oxidative stress
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Citation:
Blood. 2026 Jul 16;148(3):376-388. doi: 10.1182/blood.2025031756. PMID: 41785329; PMCID: PMC13098563 Epub:
Not Epub Abstract:
Protein disulfide isomerase (PDI) functions in thrombus formation in vivo and represents a viable target for antithrombotic... Delivery Method:
intravenous (i.v.) injection Organism or Cell Type:
C57Bl/6J and R120D PDI mutant mice Citation Extract: Yang M, Owegie OC, Patel A, Kennedy QP, Flaumenhaft JT, Chinnaraj M, Ponzar N, Fulcidor EM, Rico MC, Bhowmik A, Carroll KS, Handy DE, Loscalzo J, Essex DW, Pozzi N, Flaumenhaft R. Oxidized PDI promotes thrombus formation in oxidative stress. Blood. 2026 Jul 16;148(3):376-388. doi: 10.1182/blood.2025031756. PMID: 41785329; PMCID: PMC13098563. |
SIX1 branchio-oto-renal syndrome variants have different effects on embryonic craniofacial gene expression and cartilage formation
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Citation:
Development. 2026 Jul 1;153(13):dev205428. doi: 10.1242/dev.205428. Epub 2026 Jul 6. PMID: 42290293 Epub:
Not Epub Abstract:
SIX1 variants underlying branchio-oto-renal syndrome occur in the SIX domain (SD) or homeodomain (HD). We tested whether... Delivery Method:
microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Coppenrath K, Shaidani NI, Naert T, Majumdar HD, Horb M, Lienkamp SS, Klein SL, Moody SA. SIX1 branchio-oto-renal syndrome variants have different effects on embryonic craniofacial gene expression and cartilage formation. Development. 2026 Jul 1;153(13):dev205428. doi: 10.1242/dev.205428. Epub 2026 Jul 6. PMID: 42290293. |
LINC00607 facilitates endothelial VEGF-A receptor FLT1 splicing
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Citation:
Mol Ther. 2026 Jul 1;34(7):4323-4338. doi: 10.1016/j.ymthe.2026.03.038. Epub 2026 Apr 4. PMID: 41935951; PMCID: PMC13330067 Epub:
Not Epub Abstract:
Angiogenesis is a key function of vascular endothelial cells and becomes aberrant in pathologies such as preeclampsia. An... Link:
Delivery Method:
electroporation Organism or Cell Type:
human umbilical vein endothelial cells (HUVECs) Citation Extract: Lam F, Warwick T, Oo JA, Krüger AY, Kreis NN, Diagel A, Izquierdo Ponce J, Tirunagari P, Bayer ME, Nonn O, Dechend R, Walther T, Boon RA, Baker AH, Günther S, Wittig I, Chen Z, Müller-McNicoll M, Louwen F, Brandes RP, Leisegang MS. LINC00607 facilitates endothelial VEGF-A receptor FLT1 splicing. Mol Ther. 2026 Jul 1;34(7):4323-4338. doi: 10.1016/j.ymthe.2026.03.038. Epub 2026 Apr 4. PMID: 41935951; PMCID: PMC13330067. |
ATP6V1B2 Regulating Autophagy Flux To Affect Abnormal Auditory Development
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Citation:
Appl Biochem Biotechnol. 2026 Jul;198(7):5330-5345. doi: 10.1007/s12010-025-05579-5. Epub 2026 Apr 17. PMID: 41995948 Epub:
Not Epub Abstract:
To investigate the expression changes of ATP6V1B2 downregulation in Dominant Deafness-Onychodystrophy syndrome (DDOD syndrome... Delivery Method:
cochlear microinjection Organism or Cell Type:
mice Citation Extract: Feng Z, Li J, Yang Y, Chen M, Wu X, Zhou C. ATP6V1B2 Regulating Autophagy Flux To Affect Abnormal Auditory Development. Appl Biochem Biotechnol. 2026 Jul;198(7):5330-5345. doi: 10.1007/s12010-025-05579-5. Epub 2026 Apr 17. PMID: 41995948. |
Exploring neutral backbones in phosphorodiamidate morpholino oligomers: synthesis and biophysical properties
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Citation:
Chem Commun (Camb). 2026 Jun 25. doi: 10.1039/d6cc01842d. Epub ahead of print. PMID: 42347830 Epub:
Not Epub Abstract:
The synthesis of morpholino dimer chlorophosphoramidates and phosphoramidites has been successfully achieved and the method has... Delivery Method:
none Organism or Cell Type:
PMO-DNA and PMO-RNA Citation Extract: Das A, Kuilya D, Sharma SN, Sinha S. Exploring neutral backbones in phosphorodiamidate morpholino oligomers: synthesis and biophysical properties. Chem Commun (Camb). 2026 Jun 25. doi: 10.1039/d6cc01842d. Epub ahead of print. PMID: 42347830. |
Rapid and sensitive detection of RNA biomarkers using morpholino-functionalized organic electrochemical transistor
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Citation:
Chemical Engineering Journal. Volume 533, 2026, 174656. ISSN 1385-8947. doi: 10.1016/j.cej.2026.174656 Epub:
Not Epub Abstract:
Ribonucleic acid (RNA) biomarkers have emerged as vital molecular indicators in precision medicine, with accurate detection... Delivery Method:
none Organism or Cell Type:
SARS-CoV-2 viral RNA Citation Extract: Zhou R, Yang Q, Yang Q, Yu J, Zheng J, Yan H, Jiang X, Chen M, Liang Z, Jia Y, Segal E, Dong H, Guo K. Rapid and sensitive detection of RNA biomarkers using morpholino-functionalized organic electrochemical transistor. Chemical Engineering Journal. Volume 533, 2026, 174656. ISSN 1385-8947. doi: 10.1016/j.cej.2026.174656. |
A Splice-Site Variant in ACY1 Associated with Congenital Hearing Loss: Clinical, Biochemical, and Zebrafish Functional Evidence
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Citation:
Biochem Genet. 2026 Jun 20. doi: 10.1007/s10528-026-11417-y. Epub ahead of print. PMID: 42322530 Epub:
Not Epub Abstract:
Variants in the aminoacylase 1 (ACY1) gene are associated with diverse clinical phenotypes, but their roles in hearing loss... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Yu S, Xu Z, Wang H, Chen L, Hu SW, Zhang Y, Lyu H, Wu H, Wu M, Shu Y, Chen W. A Splice-Site Variant in ACY1 Associated with Congenital Hearing Loss: Clinical, Biochemical, and Zebrafish Functional Evidence. Biochem Genet. 2026 Jun 20. doi: 10.1007/s10528-026-11417-y. Epub ahead of print. PMID: 42322530. |
