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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 12245 scientific papers returned from the database with the search filters currently being used below.

Highly clustered de novo frameshift variants in the neuronal splicing factor NOVA2 result in a specific abnormal C terminal part and cause a severe form of intellectual disability with autistic features

Authors:
Mattioli F, Hayot G, Drouot N, Isidor B, Courraud J, Mau-Them FT, Sellier C, Hinckelmann M-V, Goldman A, Telegrafi A, Boughton A, Gamble C, Moutton S, Quartier A, Jean N, Van Ness P, Grotto S, Nambot S, Douglas G, Si YC, Chelly J, Shad Z, Kaplan E, Dineen R, Golzio C, Charlet N, Jean-Louis M, Amélie P
Citation:
bioRxiv. 2019;[preprint] doi:10.1101/858696
Epub:
Not Epub
Abstract:
The Neuro-Oncological Ventral Antigen 2 NOVA2 protein is a major factor regulating neuron specific alternative splicing,...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Mattioli F, Hayot G, Drouot N, Isidor B, Courraud J, Mau-Them FT, Sellier C, Hinckelmann M-V, Goldman A, Telegrafi A, Boughton A, Gamble C, Moutton S, Quartier A, Jean N, Van Ness P, Grotto S, Nambot S, Douglas G, Si YC, Chelly J, Shad Z, Kaplan E, Dineen R, Golzio C, Charlet N, Jean-Louis M, Amélie P. Highly clustered de novo frameshift variants in the neuronal splicing factor NOVA2 result in a specific abnormal C terminal part and cause a severe form of intellectual disability with autistic features. bioRxiv. 2019;[preprint] doi:10.1101/858696 .

Hcfc1a regulates neural precursor proliferation and asxl1 expression in the developing brain

Authors:
Castro VL, Reyes JF, Reyes-Nava N, Paz D, Quintana AM
Citation:
BMC Neurology (In Review). 2019;[preprint] doi:10.21203/rs.2.18231/v1
Epub:
Not Epub
Abstract:
Background: Precise regulation of neural precursor cell (NPC) proliferation and differentiation is essential to ensure proper...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Castro VL, Reyes JF, Reyes-Nava N, Paz D, Quintana AM. Hcfc1a regulates neural precursor proliferation and asxl1 expression in the developing brain. BMC Neurology (In Review). 2019;[preprint] doi:10.21203/rs.2.18231/v1.

Hand2 inhibits kidney specification while promoting vein formation within the posterior mesoderm

Authors:
Perens EA, Garavito-Aguilar ZV, Guio-Vega GP, Peña KT, Schindler YL, Yelon D
Citation:
Elife. 2016 Nov 2;5. pii: e19941. doi: 10.7554/eLife.19941
Epub:
Not Epub
Abstract:
Proper organogenesis depends upon defining the precise dimensions of organ progenitor territories. Kidney progenitors originate...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Perens EA, Garavito-Aguilar ZV, Guio-Vega GP, Peña KT, Schindler YL, Yelon D. Hand2 inhibits kidney specification while promoting vein formation within the posterior mesoderm. Elife. 2016 Nov 2;5. pii: e19941. doi: 10.7554/eLife.19941.

Endosome-Mediated Epithelial Remodeling Downstream of Hedgehog-Gli Is Required for Tracheoesophageal Separation

Authors:
Nasr T, Mancini P, Rankin SA, Edwards NA, Agricola ZN, Kenny AP, Kinney JL, Daniels K, Vardanyan J, Han L, Trisno SL, Cha SW, Wells JM, Kofron MJ, Zorn AM
Citation:
Dev Cell. 2019 Nov 20. pii: S1534-5807(19)30911-6. doi: 10.1016/j.devcel.2019.11.003. [Epub ahead of print]
Epub:
Yes
Abstract:
The trachea and esophagus arise from the separation of a common foregut tube during early fetal development. Mutations in key...
Delivery Method:
microinjection
Organism or Cell Type:
Xenopus laevis
Citation Extract:
Nasr T, Mancini P, Rankin SA, Edwards NA, Agricola ZN, Kenny AP, Kinney JL, Daniels K, Vardanyan J, Han L, Trisno SL, Cha SW, Wells JM, Kofron MJ, Zorn AM. Endosome-Mediated Epithelial Remodeling Downstream of Hedgehog-Gli Is Required for Tracheoesophageal Separation. Dev Cell. 2019 Nov 20. pii: S1534-5807(19)30911-6. doi: 10.1016/j.devcel.2019.11.003. [Epub ahead of print].

Isl1 Regulation of Nkx2.1 in the Early Foregut Epithelium Is Required for Trachea-Esophageal Separation and Lung Lobation

Authors:
Kim E, Jiang M, Huang H, Zhang Y, Tjota N, Gao X, Robert J, Gilmore N, Gan L, Que J
Citation:
Dev Cell. 2019 Nov 20. pii: S1534-5807(19)30910-4. doi: 10.1016/j.devcel.2019.11.002. [Epub ahead of print]
Epub:
Yes
Abstract:
The esophagus and trachea arise from the dorsal and ventral aspects of the anterior foregut, respectively. Abnormal trachea-...
Organism or Cell Type:
Xenopus laevis
Citation Extract:
Kim E, Jiang M, Huang H, Zhang Y, Tjota N, Gao X, Robert J, Gilmore N, Gan L, Que J. Isl1 Regulation of Nkx2.1 in the Early Foregut Epithelium Is Required for Trachea-Esophageal Separation and Lung Lobation. Dev Cell. 2019 Nov 20. pii: S1534-5807(19)30910-4. doi: 10.1016/j.devcel.2019.11.002. [Epub ahead of print].

The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration

Authors:
Schwenty-Lara J, Nehl D, Borchers A
Citation:
Hum Mol Genet. 2019 Dec 9. pii: ddz284. doi: 10.1093/hmg/ddz284. [Epub ahead of print]
Epub:
Yes
Abstract:
Kabuki syndrome is an autosomal dominant developmental disorder with high similarities to CHARGE syndrome. It is characterized...
Delivery Method:
microinjection
Organism or Cell Type:
Xenopus
Citation Extract:
Schwenty-Lara J, Nehl D, Borchers A. The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration. Hum Mol Genet. 2019 Dec 9. pii: ddz284. doi: 10.1093/hmg/ddz284. [Epub ahead of print].

High-throughput custom capture sequencing identifies novel mutations in coloboma-associated genes: Mutation in DNA-binding domain of retinoic acid receptor beta affects nuclear localization causing ocular coloboma

Authors:
Kalaskar VK, Alur RP, Li LK, Thomas JW, Sergeev YV, Blain D, Hufnagel RB, Cogliati T, Brooks BP
Citation:
Hum Mutat. 2019 Dec 9. doi: 10.1002/humu.23954. [Epub ahead of print]
Epub:
Yes
Abstract:
Uveal coloboma is a potentially blinding congenital ocular malformation caused by the failure of optic fissure closure during...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Kalaskar VK, Alur RP, Li LK, Thomas JW, Sergeev YV, Blain D, Hufnagel RB, Cogliati T, Brooks BP. High-throughput custom capture sequencing identifies novel mutations in coloboma-associated genes: Mutation in DNA-binding domain of retinoic acid receptor beta affects nuclear localization causing ocular coloboma. Hum Mutat. 2019 Dec 9. doi: 10.1002/humu.23954. [Epub ahead of print].

The master transcription factor SOX2, mutated in anophthalmia/microphthalmia, is post-transcriptionally regulated by the conserved RNA-binding protein RBM24 in vertebrate eye development

Authors:
Dash S, Brastrom LK, Patel SD, Scott CA, Slusarski DC, Lachke SA
Citation:
Hum Mol Genet. 2019 Dec 9. pii: ddz278. doi: 10.1093/hmg/ddz278. [Epub ahead of print]
Epub:
Yes
Abstract:
Mutations in the key transcription factor, SOX2, alone account for 20% of anophthalmia (no eye) and microphthalmia (small eye)...
Organism or Cell Type:
zebrafish
Citation Extract:
Dash S, Brastrom LK, Patel SD, Scott CA, Slusarski DC, Lachke SA. The master transcription factor SOX2, mutated in anophthalmia/microphthalmia, is post-transcriptionally regulated by the conserved RNA-binding protein RBM24 in vertebrate eye development. Hum Mol Genet. 2019 Dec 9. pii: ddz278. doi: 10.1093/hmg/ddz278. [Epub ahead of print].

EFTUD2 gene deficiency disrupts osteoblast maturation and inhibits chondrocyte differentiation via activation of the p53 signaling pathway

Authors:
Wu J, Yang Y, He Y, Li Q, Wang X, Sun C, Wang L, An Y, Luo F
Citation:
Hum Genomics. 2019 Dec 5;13(1):63. doi: 10.1186/s40246-019-0238-y
Epub:
Not Epub
Abstract:
BACKGROUND: Mandibulofacial dysostosis with microcephaly (MFDM) is characteristic of multiple skeletal anomalies comprising...
Organism or Cell Type:
zebrafish
Citation Extract:
Wu J, Yang Y, He Y, Li Q, Wang X, Sun C, Wang L, An Y, Luo F. EFTUD2 gene deficiency disrupts osteoblast maturation and inhibits chondrocyte differentiation via activation of the p53 signaling pathway. Hum Genomics. 2019 Dec 5;13(1):63. doi: 10.1186/s40246-019-0238-y.

Glis3 as a critical regulator of thyroid primordium specification

Authors:
Rurale G, Marelli F, Duminuco P, Persani L
Citation:
Thyroid. 2019 Dec 4. doi: 10.1089/thy.2019.0196. [Epub ahead of print]
Epub:
Yes
Abstract:
BACKGROUND: GLIS3 (GLI-Similar protein 3) is a transcription factor involved in several cellular processes. Homozygous...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Rurale G, Marelli F, Duminuco P, Persani L. Glis3 as a critical regulator of thyroid primordium specification. Thyroid. 2019 Dec 4. doi: 10.1089/thy.2019.0196. [Epub ahead of print].

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