Found 7 results
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2018
Hernandez N, Melki I, Jing H, Habib T, S Y Huang S, Danielson J, Kula T, Drutman S, Belkaya S, Rattina V et al..  2018.  Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency.. J Exp Med. 215(10):2567-2585.
2017
Wang W, Perens EA, Oikonomou G, Wallace SW, Lu Y, Shaham S.  2017.  IGDB-2, an Ig/FNIII protein, binds the ion channel LGC-34 and controls sensory compartment morphogenesis in C. elegans.. Dev Biol. 430(1):105-112.
2016
Paquet D, Kwart D, Chen A, Sproul A, Jacob S, Teo S, Olsen KMoore, Gregg A, Noggle S, Tessier-Lavigne M.  2016.  Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9.. Nature. 533(7601):125-9.
2015
Zhu Z, Verma N, González F, Shi Z-D, Huangfu D.  2015.  A CRISPR/Cas-Mediated Selection-free Knockin Strategy in Human Embryonic Stem Cells.. Stem Cell Reports. 4(6):1103-11.
2014
González F, Zhu Z, Shi Z-D, Lelli K, Verma N, Li QV, Huangfu D.  2014.  An iCRISPR platform for rapid, multiplexable, and inducible genome editing in human pluripotent stem cells.. Cell Stem Cell. 15(2):215-226.
2012
Cederquist GY, Luchniak A, Tischfield MA, Peeva M, Song Y, Menezes MP, Chan W-M, Andrews C, Chew S, Jamieson RV et al..  2012.  An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.. Hum Mol Genet. 21(26):5484-99.
2001
Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, Lavery T, Kouyoumjian R, Farhadian SF, Ward R et al..  2001.  Linkage disequilibrium in the human genome.. Nature. 411(6834):199-204.