खोज परिणाम - Hoffman, Ellen

  • प्रदर्शित 1 - 13 परिणाम 13
परिणाम को परिष्कृत करें
  1. 1
    Zebrafish: A Translational Model System for Studying Neuropsychiatric Disorders

    Zebrafish: A Translational Model System for Studying Neuropsychiatric Disorders द्वारा Ijaz, Sundas, Hoffman, Ellen J.

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  2. 2
    Zebrafish Models of Neurodevelopmental Disorders: Past, Present, and Future

    Zebrafish Models of Neurodevelopmental Disorders: Past, Present, and Future द्वारा Sakai, Catalina, Ijaz, Sundas, Hoffman, Ellen J.

    प्रकाशित 2018
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  3. 3
    Signaling Pathways and Sex Differential Processes in Autism Spectrum Disorder

    Signaling Pathways and Sex Differential Processes in Autism Spectrum Disorder द्वारा Enriquez, Kristen D., Gupta, Abha R., Hoffman, Ellen J.

    प्रकाशित 2021
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  4. 4
    A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders

    A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders द्वारा Sakurai, Takeshi, Reichert, Jennifer, Hoffman, Ellen J., Cai, Guiqing, Jones, Hywel B., Faham, Malek, Buxbaum, Joseph D.

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  5. 5
    Effects of Ethanol on Axon Outgrowth and Branching in Developing Rat Cortical Neurons

    Effects of Ethanol on Axon Outgrowth and Branching in Developing Rat Cortical Neurons द्वारा Hoffman, Ellen J., Mintz, C. David, Wang, Sophia, McNickle, Daniel G., Salton, Stephen R.J., Benson, Deanna L.

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  6. 6
    Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a novel microduplication in ASMT

    Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a nov... द्वारा Cai, Guiqing, Edelmann, Lisa, Goldsmith, Juliet E, Cohen, Ninette, Nakamine, Alisa, Reichert, Jennifer G, Hoffman, Ellen J, Zurawiecki, Danielle M, Silverman, Jeremy M, Hollander, Eric, Soorya, Latha, Anagnostou, Evdokia, Betancur, Catalina, Buxbaum, Joseph D

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  7. 7
    A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes

    A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes द्वारा Kroll, François, Powell, Gareth T, Ghosh, Marcus, Gestri, Gaia, Antinucci, Paride, Hearn, Timothy J, Tunbak, Hande, Lim, Sumi, Dennis, Harvey W, Fernandez, Joseph M, Whitmore, David, Dreosti, Elena, Wilson, Stephen W, Hoffman, Ellen J, Rihel, Jason

    प्रकाशित 2021
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  8. 8
    PTEN mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets

    PTEN mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets द्वारा DeSpenza, Tyrone, Carlson, Marina, Panchagnula, Shreyas, Robert, Stephanie, Duy, Phan Q., Mermin-Bunnell, Nell, Reeves, Benjamin C., Kundishora, Adam, Elsamadicy, Aladine A., Smith, Hannah, Ocken, Jack, Alper, Seth L., Jin, Sheng Chih, Hoffman, Ellen J., Kahle, Kristopher T.

    प्रकाशित 2021
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  9. 9
    Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2

    Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2 द्वारा Hoffman, Ellen J., Turner, Katherine J., Fernandez, Joseph M., Cifuentes, Daniel, Ghosh, Marcus, Ijaz, Sundas, Jain, Roshan A., Kubo, Fumi, Bill, Brent R., Baier, Herwig, Granato, Michael, Barresi, Michael J. F., Wilson, Stephen W., Rihel, Jason, State, Matthew W., Giraldez, Antonio J.

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  10. 10
    De novo damaging DNA coding mutations are associated with obsessive-compulsive disorder and overlap with Tourette’s disorder and autism

    De novo damaging DNA coding mutations are associated with obsessive-compulsive disorder and overlap with Tourette’s disorder and autism द्वारा Cappi, Carolina, Oliphant, Melody E., Péter, Zsanett, Zai, Gwyneth, do Rosário, Maria Conceição, Sullivan, Catherine A. W., Gupta, Abha R., Hoffman, Ellen J., Virdee, Manmeet, Olfson, Emily, Abdallah, Sarah B., Willsey, A. Jeremy, Shavitt, Roseli G., Miguel, Euripedes C., Kennedy, James L., Richter, Margaret A., Fernandez, Thomas V.

    प्रकाशित 2019
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  11. 11
    Selection-Free Zinc-Finger Nuclease Engineering by Context-Dependent Assembly (CoDA)

    Selection-Free Zinc-Finger Nuclease Engineering by Context-Dependent Assembly (CoDA) द्वारा Sander, Jeffry D., Dahlborg, Elizabeth J., Goodwin, Mathew J., Cade, Lindsay, Zhang, Feng, Cifuentes, Daniel, Curtin, Shaun J., Blackburn, Jessica S., Thibodeau-Beganny, Stacey, Qi, Yiping, Pierick, Christopher J., Hoffman, Ellen, Maeder, Morgan L., Khayter, Cyd, Reyon, Deepak, Dobbs, Drena, Langenau, David M., Stupar, Robert M., Giraldez, Antonio J., Voytas, Daniel F., Peterson, Randall T., Yeh, Jing-Ruey J., Joung, J. Keith

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  12. 12
    Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

    Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism द्वारा Willsey, A. Jeremy, Sanders, Stephan J., Li, Mingfeng, Dong, Shan, Tebbenkamp, Andrew T., Muhle, Rebecca A., Reilly, Steven K., Lin, Leon, Fertuzinhos, Sofia, Miller, Jeremy A., Murtha, Michael T., Bichsel, Candace, Niu, Wei, Cotney, Justin, Ercan-Sencicek, A. Gulhan, Gockley, Jake, Gupta, Abha, Han, Wenqi, He, Xin, Hoffman, Ellen, Klei, Lambertus, Lei, Jing, Liu, Wenzhong, Liu, Li, Lu, Cong, Xu, Xuming, Zhu, Ying, Mane, Shrikant M., Lein, Edward S., Wei, Liping, Noonan, James P., Roeder, Kathryn, Devlin, Bernie, Šestan, Nenad, State, Matthew W.

    प्रकाशित 2013
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  13. 13
    Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus

    Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus द्वारा Jin, Sheng Chih, Dong, Weilai, Kundishora, Adam J., Panchagnula, Shreyas, Moreno-De-Luca, Andres, Furey, Charuta G., Allocco, August A., Walker, Rebecca L., Nelson-Williams, Carol, Smith, Hannah, Dunbar, Ashley, Conine, Sierra, Lu, Qiongshi, Zeng, Xue, Sierant, Michael C., Knight, James R., Sullivan, William, Duy, Phan Q., DeSpenza, Tyrone, Reeves, Benjamin C., Karimy, Jason K., Marlier, Arnaud, Castaldi, Christopher, Tikhonova, Irina R., Li, Boyang, Peña, Helena Perez, Broach, James R., Kabachelor, Edith M., Ssenyonga, Peter, Hehnly, Christine, Ge, Li, Keren, Boris, Timberlake, Andrew T., Goto, June, Mangano, Francesco T., Johnston, James M., Butler, William E., Warf, Benjamin C., Smith, Edward R., Schiff, Steven J., Limbrick, David D., Heuer, Gregory, Jackson, Eric M., Iskandar, Bermans J., Mane, Shrikant, Haider, Shozeb, Guclu, Bulent, Bayri, Yasar, Sahin, Yener, Duncan, Charles C., Apuzzo, Michael L. J., DiLuna, Michael L., Hoffman, Ellen J., Sestan, Nenad, Ment, Laura R., Alper, Seth L., Bilguvar, Kaya, Geschwind, Daniel H., Günel, Murat, Lifton, Richard P., Kahle, Kristopher T.

    प्रकाशित 2020
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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