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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 12132 scientific papers returned from the database with the search filters currently being used below.

DOCK3 is a dosage-sensitive regulator of skeletal muscle and Duchenne muscular dystrophy-associated pathologies

Authors:
Reid AL, Wang Y, Samani A, Hightower RM, Lopez MA, Shawn R Gilbert, Ianov L, Crossman DK, Italia LJD, Millay DP, van Groen T, Halade GV, Alexander MS
Citation:
bioRxiv. 2020;[preprint] doi:10.1101/2020.03.27.010223
Epub:
Not Epub
Abstract:
DOCK3 is a member of the DOCK family of guanine nucleotide exchange factors that function to regulate cell migration, fusion,...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Reid AL, Wang Y, Samani A, Hightower RM, Lopez MA, Shawn R Gilbert, Ianov L, Crossman DK, Italia LJD, Millay DP, van Groen T, Halade GV, Alexander MS. DOCK3 is a dosage-sensitive regulator of skeletal muscle and Duchenne muscular dystrophy-associated pathologies. bioRxiv. 2020;[preprint] doi:10.1101/2020.03.27.010223 .

Triploidization Disrupts Early Reproductive Development of Females and Alters Phenotypic Sex Ratios of Sablefish Anoplopoma fimbria

Authors:
Luckenbach JA, Hayman ES, Fairgrieve WT, Wong T-T, Zohar Y, Huynh TB
Citation:
Presentation at Aquaculture America 2020, Honolulu Hawaii
Epub:
Not Epub
Abstract:
Escapement is an ecological concern for marine finfishes reared in net-pen systems. To mitigate this risk, we have initiated...
Delivery Method:
Vivo-Morpholino bathing
Organism or Cell Type:
Anoplopoma fimbria (black cod)
Citation Extract:
Luckenbach JA, Hayman ES, Fairgrieve WT, Wong T-T, Zohar Y, Huynh TB. Triploidization Disrupts Early Reproductive Development of Females and Alters Phenotypic Sex Ratios of Sablefish Anoplopoma fimbria. Presentation at Aquaculture America 2020, Honolulu Hawaii.

Live imaging defines the dynamics and molecular basis of in vivo mitophagy

Authors:
Wrighton PJ, Shwartz A, Heo J-M, Quenzer ED, LaBella KA, Harper JW, Wolfram Goessling W
Citation:
bioRxiv. 2020;[preprint] doi:10.1101/2020.03.26.010405
Epub:
Not Epub
Abstract:
Mitophagy defects are linked to aging, sarcopenia, and neurodegenerative diseases. To target this process for clinical...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Wrighton PJ, Shwartz A, Heo J-M, Quenzer ED, LaBella KA, Harper JW, Wolfram Goessling W. Live imaging defines the dynamics and molecular basis of in vivo mitophagy. bioRxiv. 2020;[preprint] doi:10.1101/2020.03.26.010405 .

GABA-Induced GnRH Release Triggers Chordate Metamorphosis

Authors:
Hozumi A, Matsunobu S, Mita K, Treen N, Sugihara T, Horie T, Sakuma T, Yamamoto T, Shiraishi A, Hamada M, Satoh N, Sakurai K, Satake H, Sasakura Y
Citation:
Curr Biol. 2020;[Epub ahead of print] doi:10.1016/j.cub.2020.02.003
Epub:
Yes
Abstract:
Metamorphosis, a widespread life history strategy in metazoans, allows dispersal and use of different ecological niches through...
Delivery Method:
microinjection
Organism or Cell Type:
Ciona intentinalis (ascidian)
Citation Extract:
Hozumi A, Matsunobu S, Mita K, Treen N, Sugihara T, Horie T, Sakuma T, Yamamoto T, Shiraishi A, Hamada M, Satoh N, Sakurai K, Satake H, Sasakura Y. GABA-Induced GnRH Release Triggers Chordate Metamorphosis. Curr Biol. 2020;[Epub ahead of print] doi:10.1016/j.cub.2020.02.003.

Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52

Authors:
D’Amore A, Tessa A, Naef V, Bassi MT, Citterio A, Romaniello R, Fichi G, Galatolo D, Mero S, Battini R, Bertocci G, Baldacci J, Sicca F, Gemignani F, Ricca I, Rubegni A, Hirst J, Marchese M, Sahin M, Ebrahimi‐Fakhari D, Filippo M. Santorelli FM
Citation:
Ann Clin Transl Neurol. 2020;[Epub] doi:10.1002/acn3.51018
Epub:
Yes
Abstract:
Autosomal recessive spastic paraplegia 52 is caused by biallelic mutations in AP4S1 which encodes a subunit of the adaptor...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
D’Amore A, Tessa A, Naef V, Bassi MT, Citterio A, Romaniello R, Fichi G, Galatolo D, Mero S, Battini R, Bertocci G, Baldacci J, Sicca F, Gemignani F, Ricca I, Rubegni A, Hirst J, Marchese M, Sahin M, Ebrahimi‐Fakhari D, Filippo M. Santorelli FM. Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52. Ann Clin Transl Neurol. 2020;[Epub] doi:10.1002/acn3.51018.

Function of Arl4aa in the Initiation of Hematopoiesis in Zebrafish by Maintaining Golgi Complex Integrity in Hemogenic Endothelium

Authors:
Guo Y, Cheng BYL, Wang D, Ma ACH, He B-L, Man TK, Cheung MPL, Shi X, Ng NKL, Leung AYH
Citation:
Stem Cell Rep. 2020;[Epub ahead of print] doi:10.1016/j.stemcr.2020.02.012
Epub:
Yes
Abstract:
ADP-ribosylation factor-like 4aa (Arl4aa) is a member of the ADP-ribosylation factor family. It is expressed in hematopoietic...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Guo Y, Cheng BYL, Wang D, Ma ACH, He B-L, Man TK, Cheung MPL, Shi X, Ng NKL, Leung AYH. Function of Arl4aa in the Initiation of Hematopoiesis in Zebrafish by Maintaining Golgi Complex Integrity in Hemogenic Endothelium. Stem Cell Rep. 2020;[Epub ahead of print] doi:10.1016/j.stemcr.2020.02.012.

De Novo Phosphoinositide Synthesis in Zebrafish Is Required for Triad Formation but Not Essential for Myogenesis

Authors:
Dowling JJ, Smith L, Fabian L, Al-Maawali A, Noche RR
Citation:
bioRxiv. 2020;[preprint] doi:10.1101/2020.03.24.005306
Epub:
Not Epub
Abstract:
Phosphoinositides (PIPs) and their regulatory enzymes are key players in many cellular processes and are required for aspects...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Dowling JJ, Smith L, Fabian L, Al-Maawali A, Noche RR. De Novo Phosphoinositide Synthesis in Zebrafish Is Required for Triad Formation but Not Essential for Myogenesis. bioRxiv. 2020;[preprint] doi:10.1101/2020.03.24.005306.

The failure of microglia to digest developmental apoptotic cells contributes to the pathology of RNASET2‐deficient leukoencephalopathy

Authors:
Hamilton N, Rutherford HA, Petts JJ, Isles HM, Weber T, Henneke M, Gärtner J, Dunning M, Renshaw SA
Citation:
Glia. 2020;[Epub ahead of print] doi:10.1002/glia.23829
Epub:
Yes
Abstract:
The contribution of microglia in neurological disorders is emerging as a leading disease driver rather than a consequence of...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Hamilton N, Rutherford HA, Petts JJ, Isles HM, Weber T, Henneke M, Gärtner J, Dunning M, Renshaw SA. The failure of microglia to digest developmental apoptotic cells contributes to the pathology of RNASET2‐deficient leukoencephalopathy. Glia. 2020;[Epub ahead of print] doi:10.1002/glia.23829.

BMP Signaling Gradient Scaling in the Zebrafish Pectoral Fin

Authors:
Mateus R, Holtzer L, Seum C, Hadjivasiliou Z, Dubois M, Jülicher F, Gonzalez-Gaitan M
Citation:
Cell Rep. 2020;30(12):4292-302.e7 doi:10.1016/j.celrep.2020.03.024
Epub:
Not Epub
Abstract:
Secreted growth factors can act as morphogens that form spatial concentration gradients in developing organs, thereby...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Mateus R, Holtzer L, Seum C, Hadjivasiliou Z, Dubois M, Jülicher F, Gonzalez-Gaitan M. BMP Signaling Gradient Scaling in the Zebrafish Pectoral Fin. Cell Rep. 2020;30(12):4292-302.e7 doi:10.1016/j.celrep.2020.03.024.

Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease

Authors:
Buglo E, Sarmiento E, Martuscelli NB, Sant DW, Danzi MC, Abrams AJ, Dallman JE, Züchner S
Citation:
PLoS ONE. 2020;15(3):e0230566. doi:10.1371/journal.pone.0230566
Epub:
Not Epub
Abstract:
A phenomenon of genetic compensation is commonly observed when an organism with a disease-bearing mutation shows incomplete...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Buglo E, Sarmiento E, Martuscelli NB, Sant DW, Danzi MC, Abrams AJ, Dallman JE, Züchner S. Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease. PLoS ONE. 2020;15(3):e0230566. doi:10.1371/journal.pone.0230566.

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