Zobrazeno 1 - 10
of 209
pro vyhledávání: '"A. E. Rubenstein"'
Autor:
Lisa Brauer Oliveira, Mauro Geller, Karin Soares Cunha, Alessandra Santos, Allan Bernacchi, Allan E. Rubenstein, Sanyu Takirambudde, Spyros Mezitis, Carolina de Almeida Ito Brum, Luiz Guilherme Darrigo, Jr., Marcia Gonçalves Ribeiro
Publikováno v:
Heliyon, Vol 7, Iss 3, Pp e06518- (2021)
Background: Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder with a prevalence of 1:3000 births and a wide variety of clinical manifestations. Cutaneous neurofibromas (cNF) are among the most common visible manifestations of N
Externí odkaz:
https://doaj.org/article/e95f9d36d332450080eff3f7ff96a63f
Publikováno v:
The Journal of Prosthetic Dentistry. 129:247-250
Osteopetrosis (marble bone disease) is a family of rare genetic disorders characterized by impaired osteoclast function leading to hyperdense, hypovascular, brittle bone. Typical imaging shows increased bone mass and thickened cortical and trabecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d893cc8652403b551033ea80e1ab1f74
https://doi.org/10.1016/j.prosdent.2021.06.024
https://doi.org/10.1016/j.prosdent.2021.06.024
Autor:
Mutlu Özcan, Jeffrey E. Rubenstein, Mohammed M. Methani, Marta Revilla-León, Wael Att, Wenceslao Piedra-Cascón
Publikováno v:
The Journal of Prosthetic Dentistry. 129:160-165
Photogrammetry technology has been used for the digitalization of multiple dental implants, but its trueness and precision remain uncertain.The purpose of this in vitro investigation was to compare the accuracy (trueness and precision) of multisite i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8527cb7b4235c845261519f24904d50f
https://doi.org/10.1016/j.prosdent.2021.05.019
https://doi.org/10.1016/j.prosdent.2021.05.019
Autor:
Alessandra Santos, Mauro Geller, Spyros Mezitis, Allan E Rubenstein, Lisa Oliveira, Daniel JM Medeiros Lima, Mendel Suchmacher Neto, Rafael Nigri, Karin Gonçalves Soares Cunha, Sanyu Takirambudde, Marcia Gonçalves Ribeiro
Publikováno v:
Clinical Pathology, Vol 13 (2020)
Introduction: Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant genetic disorders. Some clinical manifestations are present at birth, while some develop during childhood, and others can occur at any age. Given the early age
Externí odkaz:
https://doaj.org/article/5ee9f8927324419a9a417b2b782e36f8
Autor:
Marco Giovannini, Allan E. Rubenstein, Stanley F. Nelson, Zahara M. Jaffer, Jeremie Vitte, Cory H. White, Ruihong Chen, Michiko Niwa-Kawakita, Jan Manent, Walter J. Jessen, Fabrice Chareyre, Ascia Eskin, Karo Tanaka
Supplementary Materials - PDF files 113K, Materials and Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1babe054ff3e0ba7cfc7046cf73aafb1
https://doi.org/10.1158/1078-0432.22450142.v1
https://doi.org/10.1158/1078-0432.22450142.v1
Autor:
Marco Giovannini, Allan E. Rubenstein, Stanley F. Nelson, Zahara M. Jaffer, Jeremie Vitte, Cory H. White, Ruihong Chen, Michiko Niwa-Kawakita, Jan Manent, Walter J. Jessen, Fabrice Chareyre, Ascia Eskin, Karo Tanaka
Purpose: The growth and survival of neurofibromatosis type 2 (NF2)–deficient cells are enhanced by the activation of multiple signaling pathways including ErbBs/IGF-1R/Met, PI3K/Akt, and Ras/Raf/Mek/Erk1/2. The chaperone protein HSP90 is essential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::992944eb4a6ab43c00b7bc780e26e4a6
https://doi.org/10.1158/1078-0432.c.6521864.v1
https://doi.org/10.1158/1078-0432.c.6521864.v1
Autor:
Marco Giovannini, Allan E. Rubenstein, Stanley F. Nelson, Zahara M. Jaffer, Jeremie Vitte, Cory H. White, Ruihong Chen, Michiko Niwa-Kawakita, Jan Manent, Walter J. Jessen, Fabrice Chareyre, Ascia Eskin, Karo Tanaka
Supplementary Figure Legends - PDF files 65K, Figure Legends
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28b71ef6047acebf262e7fbc0441cbd2
https://doi.org/10.1158/1078-0432.22450145
https://doi.org/10.1158/1078-0432.22450145
Autor:
Marco Giovannini, Allan E. Rubenstein, Stanley F. Nelson, Zahara M. Jaffer, Jeremie Vitte, Cory H. White, Ruihong Chen, Michiko Niwa-Kawakita, Jan Manent, Walter J. Jessen, Fabrice Chareyre, Ascia Eskin, Karo Tanaka
Supplementary Figure 1 - PDF files 5795K, Induction of apoptosis by NXD30001 in NF2-deficient cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46eea79d50f8b5c5c4fe418fbe72402a
https://doi.org/10.1158/1078-0432.22450151
https://doi.org/10.1158/1078-0432.22450151
Autor:
Marco Giovannini, Allan E. Rubenstein, Stanley F. Nelson, Zahara M. Jaffer, Jeremie Vitte, Cory H. White, Ruihong Chen, Michiko Niwa-Kawakita, Jan Manent, Walter J. Jessen, Fabrice Chareyre, Ascia Eskin, Karo Tanaka
Supplementary Table 2 - XLS file 40K, qPCR validation of transcriptome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ea9981d94ba93d3b2f214cdbe4f736b
https://doi.org/10.1158/1078-0432.22450136
https://doi.org/10.1158/1078-0432.22450136
Autor:
Marco Giovannini, Allan E. Rubenstein, Stanley F. Nelson, Zahara M. Jaffer, Jeremie Vitte, Cory H. White, Ruihong Chen, Michiko Niwa-Kawakita, Jan Manent, Walter J. Jessen, Fabrice Chareyre, Ascia Eskin, Karo Tanaka
Supplementary Figure 2 - PDF files 4552K, Global transcriptome profiling of NXD30001 efficacy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa1d0b5563c6a75fb734926441a5a876
https://doi.org/10.1158/1078-0432.22450148
https://doi.org/10.1158/1078-0432.22450148