Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Melisa Ruiz-Gutierrez"'
Autor:
Claire A. Ostertag-Hill, MD, Steven J. Fishman, MD, Melisa Ruiz-Gutierrez, MD, PhD, Rush H. Chewning, MD
Publikováno v:
Journal of Vascular Surgery Cases and Innovative Techniques, Vol 9, Iss 2, Pp 101158- (2023)
Externí odkaz:
https://doaj.org/article/59a0b5d081cb49feb85bba261cadb920
Autor:
Antonio R. Perez-Atayde, Larisa Debelenko, Alyaa Al-Ibraheemi, Whitney Eng, Melisa Ruiz-Gutierrez, Meghan O’Hare, Stacy E. Croteau, Cameron C. Trenor, Debra Boyer, Daniel M. Balkin, Sarah F. Barclay, Belinda Hsi Dickie, Marilyn G. Liang, Gulraiz Chaudry, Ahmad I. Alomari, John B. Mulliken, Denise M. Adams, Kyle C. Kurek, Steven J. Fishman, Harry P.W. Kozakewich
Publikováno v:
American Journal of Surgical Pathology. 46:963-976
Autor:
Antonio R, Perez-Atayde, Larisa, Debelenko, Alyaa, Al-Ibraheemi, Whitney, Eng, Melisa, Ruiz-Gutierrez, Meghan, O'Hare, Stacy E, Croteau, Cameron C, Trenor, Debra, Boyer, Daniel M, Balkin, Sarah F, Barclay, Belinda, Hsi Dickie, Marilyn G, Liang, Gulraiz, Chaudry, Ahmad I, Alomari, John B, Mulliken, Denise M, Adams, Kyle C, Kurek, Steven J, Fishman, Harry P W, Kozakewich
Publikováno v:
The American journal of surgical pathology. 46(7)
Kaposiform lymphangiomatosis is an uncommon generalized lymphatic anomaly with distinctive clinical, radiologic, histopathologic, and molecular findings. Herein, we document the pathology in 43 patients evaluated by the Boston Children's Hospital Vas
Autor:
Chad Nusbaum, Melisa Ruiz-Gutierrez, Akiko Shimamura, Cailin E. Joyce, Colin A. Sieff, Inga Hofmann, Assieh Saadatpour, Dolly D. Thomas, Jennifer Whangbo, Kasiani C. Myers, Guo-Cheng Yuan, Towia A. Libermann, Özge Vargel Bölükbaşı, Sarah Young, Lan Jiang, Carl D. Novina
Publikováno v:
Journal of Clinical Investigation. 129:3821-3826
Shwachman-Diamond syndrome (SDS) is a rare and clinically heterogeneous bone marrow (BM) failure syndrome caused by mutations in the Shwachman-Bodian-Diamond syndrome (SBDS) gene. Although SDS was described more than 50 years ago, its molecular patho
Autor:
Mohammed H. Alomari, Mohamed M. Shahin, Steven J. Fishman, Cindy L. Kerr, Edward R. Smith, Whitney Eng, Melisa Ruiz-Gutierrez, Denise M. Adams, Darren B. Orbach, Gulraiz Chaudry, Raja Shaikh, Rush Chewning, Ahmad I. Alomari
Publikováno v:
Journal of neurosurgery. Spine.
OBJECTIVE Clinical manifestations of blue rubber bleb nevus syndrome (BRBNS) and multifocal venous malformation (MVM) vary depending on the location of the lesions. The aim of this study was to assess the risk of developing CSF leaks in patients with
Autor:
Vivian L. MacKay, Nicholas Burwick, Abdel Kareem Azab, Tomoka Nakamura, Melisa Ruiz-Gutierrez, Marilyn Sanchez-Bonilla, Michael Y. Zhang, Pilar de la Puente, Teresa S. Hyun, Akiko Shimamura, Jeffrey J. Delrow
Publikováno v:
Leukemia Research. 55:23-32
Dexamethasone (dex) induces apoptosis in multiple myeloma (MM) cells and is a frontline treatment for this disease. However resistance to dex remains a major challenge and novel treatment approaches are needed. We hypothesized that dex utilizes trans
Autor:
Kaitlyn Ballotti, Melisa Ruiz-Gutierrez, Eirini P. Papapetrou, Gabriela Alexe, Kimberly Stegmaier, Özge Vargel Bölükbaşı, Cailin E. Joyce, David W. Russell, Akiko Shimamura, Carl D. Novina, Kasiani C. Myers, Adriana G Kotini
Monosomy 7 and deletion of 7q, known as del(7q), are common clonal cytogenetic abnormalities associated with high-grade myelodysplastic syndrome (MDS) arising in inherited and acquired bone marrow failure. Current nontransplant approaches to treat ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eb971277c16044e296ce57708557cb2
https://europepmc.org/articles/PMC6629156/
https://europepmc.org/articles/PMC6629156/
Autor:
Melisa Ruiz-Gutierrez, Andriana Kotini, Özge Vargel Bölükbaşı, Gabriela Alexe, Cailin E. Joyce, Eirini P. Papapetrou, Jennifer Whangbo, David W. Russell, Akiko Shimamura, Kimberly Stegmaier, Carl D. Novina
Publikováno v:
Blood. 130:875-875
Monosomy 7 or deletion of 7q (del(7q)) are common cytogenetic abnormalities in pediatric MDS. Monosomy 7/del(7q) frequently arises in the context of inherited bone marrow failure (BMF) syndromes such as Shwachman Diamond Syndrome (SDS), an autosomal
Autor:
Ivan Topisirovic, Katherine L. B. Borden, Melisa Ruiz-Gutierrez, Biljana Culjkovic, Lucy Skrabanek
Publikováno v:
The Journal of Cell Biology
This study demonstrates that the eukaryotic translation initiation factor eIF4E is a critical node in an RNA regulon that impacts nearly every stage of cell cycle progression. Specifically, eIF4E coordinately promotes the messenger RNA (mRNA) export
Autor:
Melisa Ruiz-Gutierrez, Katherine L. B. Borden, Ivan Topisirovic, Biljana Culjkovic, Lucy Skrabanek
Publikováno v:
The Journal of Cell Biology
The eukaryotic translation initiation factor eIF4E is a critical modulator of cellular growth with functions in the nucleus and cytoplasm. In the cytoplasm, recognition of the 5′ m7G cap moiety on all mRNAs is sufficient for their functional intera