Decreased bone mineralization in Children with Noonan Syndrome: Another Consequence of Dysregulated RAS MAPKinase Pathway?

Por Choudhry, Kiran S., Grover, Monica, Tran, Alyssa, O'Brian Smith, E., Ellis, Kenneth J., Lee, Brendan H.
Publicado em 2012

The Impact of Frequency and Tone of Parent–Youth Communication on Type 1 Diabetes Management

Por DeBoer, Mark D., Valdez, Rupa, Chernavvsky, Daniel R., Grover, Monica, Burt Solorzano, Christine, Herbert, Kirabo, Patek, Stephen
Publicado no Diabetes Ther (2017)

Osteogenesis imperfecta without features of type V caused by a mutation in the IFITM5 gene

Por Grover, Monica, Campeau, Philippe M., Lietman, Caressa Dee, Lu, James T., Gibbs, Richard A., Schlesinger, Alan E., Lee, Brendan H.
Publicado em 2013

Assessment of Bone Mineral Status in Children With Marfan Syndrome

Por Grover, Monica, Brunetti-Pierri, Nicola, Belmont, John, Phan, Kelly, Tran, Alyssa, Shypailo, Roman J, Ellis, Kenneth J, Lee, Brendan H
Publicado em 2012

Losartan increases bone mass and accelerates chondrocyte hypertrophy in developing skeleton

Por Chen, Shan, Grover, Monica, Sibai, Tarek, Black, Jennifer, Rianon, Nahid, Rajagopal, Abbhirami, Munivez, Elda, Bertin, Terry, Dawson, Brian, Chen, Yuqing, Jiang, Ming-Ming, Lee, Brendan, Yang, Tao, Bae, Yangjin
Publicado no Mol Genet Metab (2015)

Hypercalcemia in Children Using the Ketogenic Diet: A Multicenter Study

Por Hawkes, Colin P, Roy, Sani M, Dekelbab, Bassem, Frazier, Britney, Grover, Monica, Haidet, Jaime, Listman, James, Madsen, Sarianne, Roan, Marian, Rodd, Celia, Sopher, Aviva, Tebben, Peter, Levine, Michael A
Publicado no J Clin Endocrinol Metab (2020)

Nitric oxide modulates bone anabolism through regulation of osteoblast glycolysis and differentiation

Por Jin, Zixue, Kho, Jordan, Dawson, Brian, Jiang, Ming-Ming, Chen, Yuqing, Ali, Saima, Burrage, Lindsay C., Grover, Monica, Palmer, Donna J., Turner, Dustin L., Ng, Philip, Nagamani, Sandesh C.S., Lee, Brendan
Publicado no J Clin Invest (2021)

Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an IFITM5 Mutation

Por Shapiro, Jay R, Lietman, Caressa, Grover, Monica, Lu, James T, Nagamani, Sandesh CS, Dawson, Brian C, Baldridge, Dustin M, Bainbridge, Matthew N, Cohn, Dan H, Blazo, Maria, Roberts, Timothy T, Brennen, Feng-Shu, Wu, Yimei, Gibbs, Richard A, Melvin, Pamela, Campeau, Philippe M, Lee, Brendan H
Publicado em 2013

Next-generation sequencing for disorders of low and high bone mineral density

Por Sule, Gautam, Campeau, Philippe M., Zhang, Victor Wei, Nagamani, Sandesh C.S., Dawson, Brian C., Grover, Monica, Bacino, Carlos A., Sutton, V. Reid, Brunetti-Pierri, Nicola, Lu, James T., Lemire, Edmond, Gibbs, Richard A., Cohn, Dan H., Cui, Hong, Wong, Lee-Jun C., Lee, Brendan H.
Publicado em 2013

WNT1 Mutations in Early-onset Osteoporosis and Osteogenesis Imperfecta

Por Laine, Christine M., Joeng, Kyu Sang, Campeau, Philippe M., Kiviranta, Riku, Tarkkonen, Kati, Grover, Monica, Lu, James T., Pekkinen, Minna, Wessman, Maija, Heino, Terhi J., Nieminen-Pihala, Vappu, Aronen, Mira, Laine, Tero, Kröger, Heikki, Cole, William G., Lehesjoki, Anna-Elina, Nevarez, Lisette, Krakow, Deborah, Curry, Cynthia J.R., Cohn, Daniel H., Gibbs, Richard A., Lee, Brendan H., Mäkitie, Outi
Publicado em 2013