Obesity during Pregnancy and Fetal Iron Status: is Hepcidin the link?

Por Dao, Maria Carlota, Sen, Sarbattama, Iyer, Chitra, Klebenov, David, Meydani, Simin Nikbin
Publicado em 2012

Neuromuscular junction transmission failure is a late phenotype in aging mice

Por Chugh, Deepti, Iyer, Chitra C., Wang, Xueyong, Bobbili, Prameela, Rich, Mark M., Arnold, W. David
Publicado no Neurobiol Aging (2019)

Deletion of atrophy enhancing genes fails to ameliorate the phenotype in a mouse model of spinal muscular atrophy

Por Iyer, Chitra C., McGovern, Vicki L., Wise, Dawnne O., Glass, David J., Burghes, Arthur H. M.
Publicado em 2014

HuD and the Survival Motor Neuron Protein Interact in Motoneurons and Are Essential for Motoneuron Development, Function, and mRNA Regulation

Por Hao le, Thi, Duy, Phan Q., An, Min, Talbot, Jared, Iyer, Chitra C., Wolman, Marc, Beattie, Christine E.
Publicado no J Neurosci (2017)

Early‐onset aging and mitochondrial defects associated with loss of histone acetyltransferase 1 (Hat1)

Por Nagarajan, Prabakaran, Agudelo Garcia, Paula A., Iyer, Chitra C., Popova, Liudmila V., Arnold, William D., Parthun, Mark R.
Publicado no Aging Cell (2019)

Conditional deletion of SMN in cell culture identifies functional SMN alleles

Por Blatnik, Anton J, McGovern, Vicki L, Le, Thanh T, Iyer, Chitra C, Kaspar, Brian K, Burghes, Arthur H M
Publicado no Hum Mol Genet (2020)

SMN expression is required in motor neurons to rescue electrophysiological deficits in the SMNΔ7 mouse model of SMA

Por McGovern, Vicki L., Iyer, Chitra C., Arnold, W. David, Gombash, Sara E., Zaworski, Phillip G., Blatnik, Anton J., Foust, Kevin D., Burghes, Arthur H.M.
Publicado no Hum Mol Genet (2015)

Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMA

Por Iyer, Chitra C., McGovern, Vicki L., Murray, Jason D., Gombash, Sara E., Zaworski, Phillip G., Foust, Kevin D., Janssen, Paul M.L., Burghes, Arthur H.M.
Publicado no Hum Mol Genet (2015)

Muscle strength and size are associated with motor unit connectivity in aged mice

Por Sheth, Kajri A., Iyer, Chitra C., Wier, Christopher G., Crum, Alexander E., Bratasz, Anna, Kolb, Stephen J., Clark, Brian C., Burghes, Arthur H.M., Arnold, W. David
Publicado no Neurobiol Aging (2018)

Muscle contractility dysfunction precedes loss of motor unit connectivity in SOD1(G93A) mice

Por Wier, Christopher G., Crum, Alexander E., Reynolds, Anthony B., Iyer, Chitra C., Chugh, Deepti, Palettas, Marilly S., Heilman, Patrick L., Kline, David M., David Arnold, W., Kolb, Stephen J.
Publicado no Muscle Nerve (2018)

SMN blood levels in a Porcine Model of Spinal Muscular Atrophy

Por Iyer, Chitra, Wang, Xueqian, Renusch, Samantha R., Duque, Sandra I., Wehr, Allison M., Mo, Xiaokui-Molly, McGovern, Vicki L., Arnold, W. David, Burghes, Arthur H.M., Kolb, Stephen J.
Publicado no J Neuromuscul Dis (2017)

Intragenic complementation of amino and carboxy terminal SMN missense mutations can rescue Smn null mice

Por McGovern, Vicki L, Kray, Kaitlyn M, Arnold, W David, Duque, Sandra I, Iyer, Chitra C, Massoni-Laporte, Aurélie, Workman, Eileen, Patel, Aalapi, Battle, Daniel J, Burghes, Arthur H M
Publicado no Hum Mol Genet (2020)

Electrophysiological biomarkers in spinal muscular atrophy: proof of concept

Por David Arnold, W, Porensky, Paul N, McGovern, Vicki L, Iyer, Chitra C, Duque, Sandra, Li, Xiaobai, Meyer, Kathrin, Schmelzer, Leah, Kaspar, Brian K, Kolb, Stephen J, Kissel, John T, Burghes, Arthur H M
Publicado em 2014

SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice

Por Gombash, Sara E., Cowley, Christopher J., Fitzgerald, Julie A., Iyer, Chitra C., Fried, David, McGovern, Vicki L., Williams, Kent C., Burghes, Arthur H.M., Christofi, Fedias L., Gulbransen, Brian D., Foust, Kevin D.
Publicado no Hum Mol Genet (2015)

SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice

Por Gombash, Sara E., Cowley, Christopher J., Fitzgerald, Julie A., Iyer, Chitra C., Fried, David, McGovern, Vicki L., Williams, Kent C., Burghes, Arthur H.M., Christofi, Fedias L., Gulbransen, Brian D., Foust, Kevin D.
Publicado no Hum Mol Genet (2015)

Mild SMN missense alleles are only functional in the presence of SMN2 in mammals

Por Iyer, Chitra C, Corlett, Kaitlyn M, Massoni-Laporte, Aurélie, Duque, Sandra I, Madabusi, Narasimhan, Tisdale, Sarah, McGovern, Vicki L, Le, Thanh T, Zaworski, Phillip G, Arnold, W David, Pellizzoni, Livio, Burghes, Arthur H M
Publicado no Hum Mol Genet (2018)

Normalization of Patient-Identified Plasma Biomarkers in SMNΔ7 Mice following Postnatal SMN Restoration

Por Arnold, W. David, Duque, Sandra, Iyer, Chitra C., Zaworski, Phillip, McGovern, Vicki L., Taylor, Shannon J., von Herrmann, Katharine M., Kobayashi, Dione T., Chen, Karen S., Kolb, Stephen J., Paushkin, Sergey V., Burghes, Arthur H. M.
Publicado no PLoS One (2016)