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Search Results - Hillin, Lori G.
Search Results - Hillin, Lori G.
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In vivo lentiviral vector gene therapy to cure hereditary tyrosinemia type 1 and prevent development of precancerous and cancerous lesions
by
Nicolas, Clara T.
,
VanLith, Caitlin J.
,
Hickey, Raymond D.
,
Du, Zeji
,
Hillin, Lori G.
,
Guthman, Rebekah M.
,
Cao, William J.
,
Haugo, Benjamin
,
Lillegard, Annika
,
Roy, Diya
,
Bhagwate, Aditya
,
O’Brien, Daniel
,
Kocher, Jean-Pierre
,
Kaiser, Robert A.
,
Russell, Stephen J.
,
Lillegard, Joseph B.
Published in
Nature communications
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Development of a porcine model of phenylketonuria with a humanized R408W mutation for gene editing
by
Kaiser, Robert A
,
Carlson, Daniel F
,
Allen, Kari L
,
Webster, Dennis A
,
VanLith, Caitlin J
,
Nicolas, Clara T
,
Hillin, Lori G
,
Yu, Yue
,
Kaiser, Catherine W
,
Wahoff, William R
,
Hickey, Raymond D
,
Watson, Adrienne L
,
Winn, Shelley R
,
Thöny, Beat
,
Kern, Douglas R
,
Harding, Cary O
,
Lillegard, Joseph B
Published in
PloS one
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Use of an adeno‐associated virus serotype Anc80 to provide durable cure of phenylketonuria in a mouse model
by
Kaiser, Robert A.
,
Weber, Nicholas D.
,
Trigueros‐Motos, Laia
,
Allen, Kari L.
,
Martinez, Michael
,
Cao, William
,
VanLith, Caitlin J.
,
Hillin, Lori G.
,
Douar, Anne
,
González‐Aseguinolaza, Gloria
,
Aldabe, Rafael
,
Lillegard, Joseph B.
Published in
Journal of inherited metabolic disease
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