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Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation.

Cell reports

Ulferts R, Marcassa E, Timimi L, Lee LC, Daley A, Montaner B, Turner SD, Florey O, Baillie JK, Beale R.
PMID: 34706226
Cell Rep. 2021 Oct 26;37(4):109899. doi: 10.1016/j.celrep.2021.109899.

Although commonly associated with autophagosomes, LC3 can also be recruited to membranes by covalent lipidation in a variety of non-canonical contexts. These include responses to ionophores such as the M2 proton channel of influenza A virus. We report a...

Cite
Ulferts R, Marcassa E, Timimi L, et al. Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation. Cell Rep. 2021;37(4):109899doi: 10.1016/j.celrep.2021.109899.
Ulferts, R., Marcassa, E., Timimi, L., Lee, L. C., Daley, A., Montaner, B., Turner, S. D., Florey, O., Baillie, J. K., & Beale, R. (2021). Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation. Cell reports, 37(4), 109899. https://doi.org/10.1016/j.celrep.2021.109899
Ulferts, Rachel, et al. "Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation." Cell reports vol. 37,4 (2021): 109899. doi: https://doi.org/10.1016/j.celrep.2021.109899
Ulferts R, Marcassa E, Timimi L, Lee LC, Daley A, Montaner B, Turner SD, Florey O, Baillie JK, Beale R. Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation. Cell Rep. 2021 Oct 26;37(4):109899. doi: 10.1016/j.celrep.2021.109899. PMID: 34706226; PMCID: PMC8567314.
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Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation.

Cell reports

Ulferts R, Marcassa E, Timimi L, Lee LC, Daley A, Montaner B, Turner SD, Florey O, Baillie JK, Beale R.
PMID: 34706226
Cell Rep. 2021 Oct 26;37(4):109899. doi: 10.1016/j.celrep.2021.109899.

Although commonly associated with autophagosomes, LC3 can also be recruited to membranes by covalent lipidation in a variety of non-canonical contexts. These include responses to ionophores such as the M2 proton channel of influenza A virus. We report a...

Cite
Ulferts R, Marcassa E, Timimi L, et al. Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation. Cell Rep. 2021;37(4):109899doi: 10.1016/j.celrep.2021.109899.
Ulferts, R., Marcassa, E., Timimi, L., Lee, L. C., Daley, A., Montaner, B., Turner, S. D., Florey, O., Baillie, J. K., & Beale, R. (2021). Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation. Cell reports, 37(4), 109899. https://doi.org/10.1016/j.celrep.2021.109899
Ulferts, Rachel, et al. "Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation." Cell reports vol. 37,4 (2021): 109899. doi: https://doi.org/10.1016/j.celrep.2021.109899
Ulferts R, Marcassa E, Timimi L, Lee LC, Daley A, Montaner B, Turner SD, Florey O, Baillie JK, Beale R. Subtractive CRISPR screen identifies the ATG16L1/vacuolar ATPase axis as required for non-canonical LC3 lipidation. Cell Rep. 2021 Oct 26;37(4):109899. doi: 10.1016/j.celrep.2021.109899. PMID: 34706226; PMCID: PMC8567314.
Copy Download .nbib Format: NLM
Showing 1 to 2 of 2 entries