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 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 en 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 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 en 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 en 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 en Hum Mol Genet (2020)

Voluntary Wheel Running with and without Follistatin Overexpression Improves NMJ Transmission but not motor unit loss in Late Life of C57BL/6J Mice

por Chugh, Deepti, Iyer, Chitra C., Bobbili, Prameela, Blatnik, Anton J., Kaspar, Brian K., Meyer, Kathrin, Burghes, Arthur HM, Clark, Brian C., Arnold, W. David
Publicado en Neurobiol Aging (2021)

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 en 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 en 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 en 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 en 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 en 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 en Hum Mol Genet (2020)

Follistatin-induced Muscle Hypertrophy in Aged mice Improves Neuromuscular Junction Innervation and Function

por Iyer, Chitra C., Chugh, Deepti, Bobbili, Prameela J., Blatnik, Anton J., Crum, Alexander E., Yi, Allen F., Kaspar, Brian K., Meyer, Kathrin C., Burghes, Arthur H.M., Arnold, W. David
Publicado en Neurobiol Aging (2021)

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 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 en 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 en 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 en 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 en PLoS One (2016)