Hasil Pencarian - Jan Hoeber

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  1. 1
    Sensory regeneration in dorsal root avulsion

    Sensory regeneration in dorsal root avulsion oleh Jan Hoeber

    Diterbitkan 2015-01-01
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  2. 2
    Generation of a human Neurochondrin deficient iPSC line KICRi002-A-3 using CRISPR/Cas9

    Generation of a human Neurochondrin deficient iPSC line KICRi002-A-3 using CRISPR/Cas9 oleh Ambrin Fatima, Jens Schuster, Talia Akram, Maria Sobol, Jan Hoeber, Niklas Dahl

    Diterbitkan 2020-04-01
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  3. 3
    Generation of two human iPSC lines (UUIGPi013-A and UUIPGi014-A) from cases with Down syndrome and full trisomy for chromosome 21 (T21)

    Generation of two human iPSC lines (UUIGPi013-A and UUIPGi014-A) from cases with Down syndrome and full trisomy for chromosome 21 (T21) oleh Jens Schuster, Jan Hoeber, Maria Sobol, Ambrin Fatima, Göran Annerén, Niklas Dahl

    Diterbitkan 2020-12-01
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  4. 4
    Incontinentia pigmenti: Generation of an IKBKG deficient human iPSC line (KICRi002-A-1) on a 46,XY background using CRISPR/Cas9

    Incontinentia pigmenti: Generation of an IKBKG deficient human iPSC line (KICRi002-A-1) on a 46,XY background using CRISPR/Cas9 oleh Ambrin Fatima, Jens Schuster, Talia Akram, Carolina Maya González, Maria Sobol, Jan Hoeber, Niklas Dahl

    Diterbitkan 2020-04-01
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  5. 5
    Mover is a homomeric phospho-protein present on synaptic vesicles.

    Mover is a homomeric phospho-protein present on synaptic vesicles. oleh Saheeb Ahmed, Nina Wittenmayer, Thomas Kremer, Jan Hoeber, Asha Kiran Akula, Henning Urlaub, Markus Islinger, Joachim Kirsch, Camin Dean, Thomas Dresbach

    Diterbitkan 2013-01-01
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  6. 6
    A VDAC1-Derived N-Terminal Peptide Inhibits Mutant SOD1-VDAC1 Interactions and Toxicity in the SOD1 Model of ALS

    A VDAC1-Derived N-Terminal Peptide Inhibits Mutant SOD1-VDAC1 Interactions and Toxicity in the SOD1 Model of ALS oleh Anna Shteinfer-Kuzmine, Shirel Argueti, Rajeev Gupta, Neta Shvil, Salah Abu-Hamad, Yael Gropper, Jan Hoeber, Andrea Magrì, Angela Messina, Elena N. Kozlova, Varda Shoshan-Barmatz, Adrian Israelson

    Diterbitkan 2019-08-01
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  7. 7
    ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function

    ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function oleh Jens Schuster, Joakim Klar, Ayda Khalfallah, Loora Laan, Jan Hoeber, Ambrin Fatima, Velin Marita Sequeira, Zhe Jin, Sergiy V. Korol, Mikael Huss, Ann Nordgren, Ann Nordgren, Britt Marie Anderlid, Britt Marie Anderlid, Caroline Gallant, Bryndis Birnir, Niklas Dahl

    Diterbitkan 2022-10-01
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