Search Results - "Moody, Tania"

Corrigendum to “ACVR1R206H extends inflammatory responses in human induced pluripotent stem cell-derived macrophages” [Bone. 153 2021 Dec; 116129. doi:10.1016/j.bone.2021.116129. Epub 2021 Jul 24. PMID: 34311122] by Matsuo, Koji, Lepinski, Abigail, Chavez, Robert D., Barruet, Emilie, Pereira, Ashley, Moody, Tania A., Ton, Amy N., Sharma, Aditi, Hellman, Judith, Tomoda, Kiichiro, Nakamura, Mary C., Hsiao, Edward C.

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ACVR1R206H extends inflammatory responses in human induced pluripotent stem cell-derived macrophages by Matsuo, Koji, Lepinski, Abigail, Chavez, Robert D., Barruet, Emilie, Pereira, Ashley, Moody, Tania A., Ton, Amy N., Sharma, Aditi, Hellman, Judith, Tomoda, Kiichiro, Nakamura, Mary C., Hsiao, Edward C.

“…Macrophages play crucial roles in many human disease processes. However, obtaining large numbers of primary cells for study is often difficult. We describe 2D…”
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NF-κB/MAPK activation underlies ACVR1-mediated inflammation in human heterotopic ossification by Barruet, Emilie, Morales, Blanca M, Cain, Corey J, Ton, Amy N, Wentworth, Kelly L, Chan, Tea V, Moody, Tania A, Haks, Mariëlle C, Ottenhoff, Tom Hm, Hellman, Judith, Nakamura, Mary C, Hsiao, Edward C

“…Inflammation helps regulate normal growth and tissue repair. Although bone morphogenetic proteins (BMPs) and inflammation are known contributors to abnormal…”
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Modeling the ACVR1R206H mutation in human skeletal muscle stem cells by Barruet, Emilie, Garcia, Steven M, Wu, Jake, Morales, Blanca M, Tamaki, Stanley, Moody, Tania, Pomerantz, Jason H, Hsiao, Edward C

“…Abnormalities in skeletal muscle repair can lead to poor function and complications such as scarring or heterotopic ossification (HO). Here, we use…”
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Modeling the ACVR1.sup.R206H mutation in human skeletal muscle stem cells by Barruet, Emilie, Garcia, Steven M, Wu, Jake, Morales, Blanca M, Tamaki, Stanley, Moody, Tania, Pomerantz, Jason H, Hsiao, Edward C

“…Abnormalities in skeletal muscle repair can lead to poor function and complications such as scarring or heterotopic ossification (HO). Here, we use…”
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Functional Testing of Bone Morphogenetic Protein (BMP) Pathway Variants Identified on Whole‐Exome Sequencing in a Patient with Delayed‐Onset Fibrodysplasia Ossificans Progressiva (FOP) Using ACVR1R206H‐Specific Human Cellular and Zebrafish Models by Wentworth, Kelly L., Lalonde, Robert L., Groppe, Jay C., Brewer, Niambi, Moody, Tania, Hansberry, Steven, Taylor, Kimberly E., Shore, Eileen M., Kaplan, Frederick S., Pignolo, Robert J., Yelick, Pamela C., Hsiao, Edward C.

“…ABSTRACT Bone morphogenetic protein (BMP) signaling is critical in skeletal development. Overactivation can trigger heterotopic ossification (HO) as in…”
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Wnt pathway inhibition with the porcupine inhibitor LGK974 decreases trabecular bone but not fibrosis in a murine model with fibrotic bone by Lung, Hsuan, Wentworth, Kelly L, Moody, Tania, Zamarioli, Ariane, Ram, Apsara, Ganesh, Gauri, Kang, Misun, Ho, Sunita, Hsiao, Edward C

“…G protein-coupled receptors (GPCRs) mediate a wide spectrum of physiological functions, including the development, remodeling, and repair of the skeleton…”
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Global Wnt Inhibition With a Porcupine Inhibitor Decreases Established Trabecular Bone in a Mouse Model of Fibrous Dysplasia by Lung, Hsuan, Moody, Tania, Wentworth, Kelly, Kang, Misun, Ho, Sunita, Hsiao, Edward

“…Abstract Background: G protein-coupled receptors (GPCRs) mediate a wide spectrum of physiological functions, including bone development and remodeling. Fibrous…”
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Modeling the ACVR1 R206H mutation in human skeletal muscle stem cells by Barruet, Emilie, Garcia, Steven M, Wu, Jake, Morales, Blanca M, Tamaki, Stanley, Moody, Tania, Pomerantz, Jason H, Hsiao, Edward C

“…Abnormalities in skeletal muscle repair can lead to poor function and complications such as scarring or heterotopic ossification (HO). Here, we use…”
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SUN-368 Wnt Inhibition Decreases Trabecular Bone in a Mouse Model of Fibrous Dysplasia by Lung, Hsuan, Wentworth, Kelly, Moody, Tania, Kang, Misun, Ho, Sunita, Hsiao, Edward

“…Abstract Background: G protein-coupled receptor (GPCR) signaling mediates a wide spectrum of physiological functions, including bone development and…”
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Functional Testing of Bone Morphogenetic Protein (BMP) Pathway Variants Identified on Whole-Exome Sequencing in a Patient with Delayed-Onset Fibrodysplasia Ossificans Progressiva (FOP) Using ACVR1 R206H -Specific Human Cellular and Zebrafish Models by Wentworth, Kelly L, Lalonde, Robert L, Groppe, Jay C, Brewer, Niambi, Moody, Tania, Hansberry, Steven, Taylor, Kimberly E, Shore, Eileen M, Kaplan, Frederick S, Pignolo, Robert J, Yelick, Pamela C, Hsiao, Edward C

“…Bone morphogenetic protein (BMP) signaling is critical in skeletal development. Overactivation can trigger heterotopic ossification (HO) as in fibrodysplasia…”
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MON-710 ACVR1 Activation in Primary and iPS-Derived Human Skeletal Muscle Stem Cells Impairs Myogenic Transcriptional Signature and Function by Barruet, Emilie, Garcia, Steven, Tamaki, Stanley, Morales, Blanca M, Wu, Jake, Moody, Tania, Pomerantz, Jason H, Hsiao, Edward Chiaming

“…Abstract Developing optimal strategies for skeletal muscle regeneration and repair requires a detailed understanding of how these processes are regulated. The…”
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Corrigendum to "ACVR1 R206H extends inflammatory responses in human induced pluripotent stem cell-derived macrophages" [Bone. 153 2021 Dec; 116129. doi:10.1016/j.bone.2021.116129. Epub 2021 Jul 24. PMID: 34311122] by Matsuo, Koji, Lepinski, Abigail, Chavez, Robert D, Barruet, Emilie, Pereira, Ashley, Moody, Tania A, Ton, Amy N, Sharma, Aditi, Hellman, Judith, Tomoda, Kiichiro, Nakamura, Mary C, Hsiao, Edward C

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ACVR1 R206H extends inflammatory responses in human induced pluripotent stem cell-derived macrophages by Matsuo, Koji, Lepinski, Abigail, Chavez, Robert D, Barruet, Emilie, Pereira, Ashley, Moody, Tania A, Ton, Amy N, Sharma, Aditi, Hellman, Judith, Tomoda, Kiichiro, Nakamura, Mary C, Hsiao, Edward C

“…Macrophages play crucial roles in many human disease processes. However, obtaining large numbers of primary cells for study is often difficult. We describe 2D…”
Get full text