24/7 Neurocritical Care Nurse Practitioner Coverage Reduced Door-to-Needle Time in Stroke Patients Treated with Tissue Plasminogen Activator

Yazar: Moran, Jennifer L., Nakagawa, Kazuma, Asai, Susan M., Koenig, Matthew A.
Yayımlandı J Stroke Cerebrovasc Dis (2016)

An N-ethyl-N-nitrosourea mutagenesis recessive screen identifies two candidate regions for murine cardiomyopathy that map to chromosomes 1 and 15

Yazar: Fernandez, Liliana, Marchuk, Douglas A., Moran, Jennifer L., Beier, David R., Rockman, Howard A.
Baskı/Yayın Bilgisi 2009

De Novo Exon Duplication in a New Allele of Mouse Glra1 (Spasmodic)

Yazar: Holland, Katherine D., Fleming, Michelle T., Cheek, Susannah, Moran, Jennifer L., Beier, David R., Meisler, Miriam H.
Baskı/Yayın Bilgisi 2006

A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis

Yazar: Tao, Jianning, Koster, Maranke I., Harrison, Wilbur, Moran, Jennifer L., Beier, David R., Roop, Dennis R., Overbeek, Paul A.
Baskı/Yayın Bilgisi 2012

Cholesterol Metabolism Is Required for Intracellular Hedgehog Signal Transduction In Vivo

Yazar: Stottmann, Rolf W., Turbe-Doan, Annick, Tran, Pamela, Kratz, Lisa E., Moran, Jennifer L., Kelley, Richard I., Beier, David R.
Baskı/Yayın Bilgisi 2011

Concurrent Lpin1 and Nrcam Mouse Mutations Result in Severe Peripheral Neuropathy with Transitory Hindlimb Paralysis

Yazar: Douglas, Darlene S., Moran, Jennifer L., Bermingham, John R., Chen, Xiang-Jun, Brindley, David N., Soliven, Betty, Beier, David R., Popko, Brian
Baskı/Yayın Bilgisi 2009

A family-based study of common polygenic variation and risk of schizophrenia

Yazar: Ruderfer, Douglas M, Kirov, George, Chambert, Kimberly, Moran, Jennifer L, Owen, Michael J, O’Donovan, Michael C, Sklar, Pamela, Purcell, Shaun M
Baskı/Yayın Bilgisi 2011

Manic fringe is not required for embryonic development, and fringe family members do not exhibit redundant functions in the axial skeleton, limb, or hindbrain

Yazar: Moran, Jennifer L., Shifley, Emily T., Levorse, John M., Mani, Shyamala, Ostmann, Kristin, Perez-Balaguer, Ariadna, Walker, Dawn M., Vogt, Thomas F., Cole, Susan E.
Baskı/Yayın Bilgisi 2009

Latent TGF-β–binding protein 4 modifies muscular dystrophy in mice

Yazar: Heydemann, Ahlke, Ceco, Ermelinda, Lim, Jackie E., Hadhazy, Michele, Ryder, Pearl, Moran, Jennifer L., Beier, David R., Palmer, Abraham A., McNally, Elizabeth M.
Baskı/Yayın Bilgisi 2009

Latent TGF-β–binding protein 4 modifies muscular dystrophy in mice

Yazar: Heydemann, Ahlke, Ceco, Ermelinda, Lim, Jackie E., Hadhazy, Michele, Ryder, Pearl, Moran, Jennifer L., Beier, David R., Palmer, Abraham A., McNally, Elizabeth M.
Baskı/Yayın Bilgisi 2010

Agouti C57BL/6N embryonic stem cells for mouse genetic resources

Yazar: Pettitt, Stephen J., Liang, Qi, Rairdan, Xin Y., Moran, Jennifer L., Prosser, Haydn M., Beier, David R., Lloyd, Kent, Bradley, Allan, Skarnes, William C.
Baskı/Yayın Bilgisi 2009

ENU Mutagenesis in Mice Identifies Candidate Genes For Hypogonadism

Yazar: Weiss, Jeffrey, Hurley, Lisa A., Harris, Rebecca M., Finlayson, Courtney, Tong, Minghan, Fisher, Lisa A., Moran, Jennifer L., Beier, David R., Mason, Christopher, Jameson, J. Larry
Baskı/Yayın Bilgisi 2012

No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia

Yazar: Ruderfer, Douglas M, Lim, Elaine T, Genovese, Giulio, Moran, Jennifer L, Hultman, Christina M, Sullivan, Patrick F, McCarroll, Steven A, Holmans, Peter, Sklar, Pamela, Purcell, Shaun M
Yayımlandı Eur J Hum Genet (2015)

A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype

Yazar: Dwyer, Noelle D, Manning, Danielle K, Moran, Jennifer L, Mudbhary, Raksha, Fleming, Michael S, Favero, Carlita B, Vock, Vita M, O'Leary, Dennis DM, Walsh, Christopher A, Beier, David R
Baskı/Yayın Bilgisi 2011

De novo CNVs in bipolar affective disorder and schizophrenia

Yazar: Georgieva, Lyudmila, Rees, Elliott, Moran, Jennifer L., Chambert, Kimberly D., Milanova, Vihra, Craddock, Nicholas, Purcell, Shaun, Sklar, Pamela, McCarroll, Steven, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Kirov, George
Yayımlandı Hum Mol Genet (2014)

Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia

Yazar: Genovese, Giulio, Fromer, Menachem, Stahl, Eli A., Ruderfer, Douglas M., Chambert, Kimberly, Landén, Mikael, Moran, Jennifer L., Purcell, Shaun M., Sklar, Pamela, Sullivan, Patrick F., Hultman, Christina M., McCarroll, Steven A.
Yayımlandı Nat Neurosci (2016)

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

Yazar: Pocklington, Andrew J., Rees, Elliott, Walters, James T.R., Han, Jun, Kavanagh, David H., Chambert, Kimberly D., Holmans, Peter, Moran, Jennifer L., McCarroll, Steven A., Kirov, George, O’Donovan, Michael C., Owen, Michael J.
Yayımlandı Neuron (2015)

Structural basis of clade-specific HIV-1 neutralization by humanized anti-V3 monoclonal antibody KD-247

Yazar: Kirby, Karen A., Ong, Yee Tsuey, Hachiya, Atsuko, Laughlin, Thomas G., Chiang, Leslie A., Pan, Yun, Moran, Jennifer L., Marchand, Bruno, Singh, Kamalendra, Gallazzi, Fabio, Quinn, Thomas P., Yoshimura, Kazuhisa, Murakami, Toshio, Matsushita, Shuzo, Sarafianos, Stefan G.
Yayımlandı FASEB J (2015)

Evidence of Common Genetic Overlap Between Schizophrenia and Cognition

Yazar: Hubbard, Leon, Tansey, Katherine E., Rai, Dheeraj, Jones, Peter, Ripke, Stephan, Chambert, Kimberly D., Moran, Jennifer L., McCarroll, Steven A., Linden, David E. J., Owen, Michael J., O’Donovan, Michael C., Walters, James T. R., Zammit, Stanley
Yayımlandı Schizophr Bull (2016)

Analysis of copy number variations at 15 schizophrenia-associated loci

Yazar: Rees, Elliott, Walters, James T. R., Georgieva, Lyudmila, Isles, Anthony R., Chambert, Kimberly D., Richards, Alexander L., Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Steven A., O’Donovan, Michael C., Owen, Michael J., Kirov, George
Baskı/Yayın Bilgisi 2014