In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice
Hutchinson–Gilford progeria syndrome (HGPS or progeria) is typically caused by a
dominant-negative C• G-to-T• A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that …
dominant-negative C• G-to-T• A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that …
In vivo base editing rescues Hutchinson-Gilford progeria syndrome in mice
LW Koblan, MR Erdos, C Wilson, WA Cabral… - …, 2021 - pubmed.ncbi.nlm.nih.gov
Hutchinson-Gilford progeria syndrome (HGPS or progeria) is typically caused by a dominant-
negative C• G-to-T• A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that encodes …
negative C• G-to-T• A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that encodes …
In vivo base editing rescues Hutchinson-Gilford progeria syndrome in mice
LW Koblan, MR Erdos, C Wilson, WA Cabral, JM Levy… - Nature, 2021 - go.gale.com
Hutchinson-Gilford progeria syndrome (HGPS or progeria) is typically caused by a dominant-
negative C* G-to-T* A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that encodes …
negative C* G-to-T* A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that encodes …
In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice
LW Koblan, MR Erdos, C Wilson, WA Cabral… - …, 2021 - pure.johnshopkins.edu
Hutchinson–Gilford progeria syndrome (HGPS or progeria) is typically caused by a
dominant-negative C• G-to-T• A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that …
dominant-negative C• G-to-T• A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that …
In vivo base editing rescues Hutchinson-Gilford progeria syndrome in mice.
LW Koblan, MR Erdos, C Wilson, WA Cabral, JM Levy… - Nature, 2021 - europepmc.org
Hutchinson-Gilford progeria syndrome (HGPS) is typically caused by a dominant-negative
C• G-to-T• A mutation (c. 1824 C> T, G608G) in LMNA, the nuclear lamin A gene. This …
C• G-to-T• A mutation (c. 1824 C> T, G608G) in LMNA, the nuclear lamin A gene. This …
[HTML][HTML] In Vivo Base Editing Rescues Hutchinson-Gilford Progeria Syndrome in Mice
LW Koblan, MR Erdos, C Wilson, WA Cabral, JM Levy… - Nature, 2021 - ncbi.nlm.nih.gov
Hutchinson-Gilford progeria syndrome (HGPS) is typically caused by a dominant-negative
C• G-to-T• A mutation (c. 1824 C> T, G608G) in LMNA, the nuclear lamin A gene. This …
C• G-to-T• A mutation (c. 1824 C> T, G608G) in LMNA, the nuclear lamin A gene. This …
In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice
LW Koblan, MR Erdos, C Wilson, WA Cabral, JM Levy… - Nature, 2021 - ideas.repec.org
Hutchinson–Gilford progeria syndrome (HGPS or progeria) is typically caused by a
dominant-negative C• G-to-T• A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that …
dominant-negative C• G-to-T• A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that …
In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice
LW Koblan, MR Erdos, C Wilson, WA Cabral, JM Levy… - Nature, 2021 - dash.harvard.edu
Hutchinson-Gilford progeria syndrome (HGPS) is typically caused by a dominant-negative
C• G-to-T• A mutation (c. 1824 C> T, G608G) in LMNA, the nuclear lamin A gene. This …
C• G-to-T• A mutation (c. 1824 C> T, G608G) in LMNA, the nuclear lamin A gene. This …
[引用 ][C] In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice
LW Koblan, MR Erdos, C Wilson, WA Cabral, JM Levy… - Nature, 2021 - cir.nii.ac.jp
In vivo base editing rescues Hutchinson-Gilford progeria syndrome in mice
LW Koblan, MR Erdos, C Wilson, WA Cabral… - …, 2021 - ui.adsabs.harvard.edu
Hutchinson-Gilford progeria syndrome (HGPS or progeria) is typically caused by a dominant-
negative C• G-to-T• A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that encodes …
negative C• G-to-T• A mutation (c. 1824 C> T; p. G608G) in LMNA, the gene that encodes …