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

par Dao, Maria Carlota, Sen, Sarbattama, Iyer, Chitra, Klebenov, David, Meydani, Simin Nikbin
Publié 2012

Neuromuscular junction transmission failure is a late phenotype in aging mice

par Chugh, Deepti, Iyer, Chitra C., Wang, Xueyong, Bobbili, Prameela, Rich, Mark M., Arnold, W. David
Publié dans Neurobiol Aging (2019)

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

par Iyer, Chitra C., McGovern, Vicki L., Wise, Dawnne O., Glass, David J., Burghes, Arthur H. M.
Publié 2014

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

par Hao le, Thi, Duy, Phan Q., An, Min, Talbot, Jared, Iyer, Chitra C., Wolman, Marc, Beattie, Christine E.
Publié dans J Neurosci (2017)

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

par Nagarajan, Prabakaran, Agudelo Garcia, Paula A., Iyer, Chitra C., Popova, Liudmila V., Arnold, William D., Parthun, Mark R.
Publié dans Aging Cell (2019)

Conditional deletion of SMN in cell culture identifies functional SMN alleles

par Blatnik, Anton J, McGovern, Vicki L, Le, Thanh T, Iyer, Chitra C, Kaspar, Brian K, Burghes, Arthur H M
Publié dans 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

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

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

par 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.
Publié dans Hum Mol Genet (2015)

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

par 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.
Publié dans Hum Mol Genet (2015)

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

par 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
Publié dans Neurobiol Aging (2018)

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

par 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.
Publié dans Muscle Nerve (2018)

SMN blood levels in a Porcine Model of Spinal Muscular Atrophy

par 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.
Publié dans J Neuromuscul Dis (2017)

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

par 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
Publié dans Hum Mol Genet (2020)

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

par 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
Publié dans Neurobiol Aging (2021)

Electrophysiological biomarkers in spinal muscular atrophy: proof of concept

par 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
Publié 2014

SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice

par 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.
Publié dans Hum Mol Genet (2015)

SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice

par 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.
Publié dans Hum Mol Genet (2015)

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

par 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
Publié dans Hum Mol Genet (2018)

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

par 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.
Publié dans PLoS One (2016)