Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Rene L Galindo"'
This book presents new insights into the etiology and pathogenesis of systemic diseases recently discovered to be due to specific defects in molecular assemblies, organelles, or other subcellular structures. This new information, of great importance
Autor:
Rene L. Galindo, Priya Mahajan, Kathleen A. Galindo, Samuel R. Scarborough, Pooja Dalal, Usha Avirneni-Vadlamudi, Valerie A. Granados
Rhabdomyosarcoma (RMS) is an aggressive soft tissue malignancy comprised histologically of skeletal muscle lineage precursors that fail to exit the cell cycle and fuse into differentiated syncytial muscle—for which the underlying pathogenetic mecha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cca5ffd45c6074f4bb27991739933e5
https://doi.org/10.1158/0008-5472.c.6511167.v1
https://doi.org/10.1158/0008-5472.c.6511167.v1
Autor:
Usha Avirneni-Vadlamudi, Kathleen A. Galindo, Samuel R. Scarborough, Pooja Dalal, Valerie A. Granados, Rene L. Galindo, Priya Mahajan
Publikováno v:
Cancer Research. 79:4585-4591
Rhabdomyosarcoma (RMS) is an aggressive soft tissue malignancy comprised histologically of skeletal muscle lineage precursors that fail to exit the cell cycle and fuse into differentiated syncytial muscle—for which the underlying pathogenetic mecha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::900357d62a819686c72847145049c082
https://doi.org/10.1158/0008-5472.can-18-2096
https://doi.org/10.1158/0008-5472.can-18-2096
Publikováno v:
Journal of Pediatric Hematology/Oncology. 37:402-405
Infantile myofibromatosis (IM) is most commonly limited to cutaneous lesions that resolve spontaneously. However, generalized IM with visceral involvement, which has a reported mortality rate as high as 73%, has been successfully treated with a combi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a93793ad2b78edbb7dc116660e8288c5
https://doi.org/10.1097/mph.0000000000000132
https://doi.org/10.1097/mph.0000000000000132
Publikováno v:
G3: Genes|Genomes|Genetics
Rhabdomyosarcoma (RMS) is an aggressive childhood malignancy of neoplastic muscle-lineage precursors that fail to terminally differentiate into syncytial muscle. The most aggressive form of RMS, alveolar-RMS, is driven by misexpression of the PAX-FOX
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f6a9391cef2d3c016c8a7015776ed8a
https://doi.org/10.1534/g3.114.015818
https://doi.org/10.1534/g3.114.015818
Publikováno v:
New-Opathies. :i-xvii
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45992a0f892426846ee06afd716e54bb
https://doi.org/10.1142/9789814355698_fmatter
https://doi.org/10.1142/9789814355698_fmatter
Autor:
Dinesh Rakheja, Kathleen S. Wilson, James F. Amatruda, Scott Cameron, Rene L. Galindo, Garvin L. Chandler, Vera Paulson
Publikováno v:
Genes, Chromosomes and Cancer. 50:397-408
Pediatric rhabdomyosarcoma occurs as two biologically distinct histological variants, embryonal (ERMS) and alveolar (ARMS). To identify genomic changes that drive ERMS pathogenesis, we used a new array comparative genomic hybridization (aCGH) platfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50c29161edce445e9749a8e86f4f11a0
https://doi.org/10.1002/gcc.20864
https://doi.org/10.1002/gcc.20864
Rhabdomyosarcoma (RMS) is a mesenchymal malignancy composed of neoplastic primitive precursor cells that exhibit histological features of myogenic differentiation. Despite intensive conventional multimodal therapy, patients with high-risk RMS typical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aeb60087a2af38da7f9a2e2c3cfe3f6
https://europepmc.org/articles/PMC4599785/
https://europepmc.org/articles/PMC4599785/
Autor:
David M. Steinberg, William H. Westra, Syed Z. Ali, Rene L. Galindo, Anil V. Parwani, Martha A. Zeiger
Publikováno v:
Diagnostic Cytopathology. 28:213-216
Solitary fibrous tumor (SFT) is an uncommon mesenchymal neoplasm that arises primarily from the pleura. Extrapleural occurrences are rare. To our knowledge, there is no published account of this entity in the thyroid in the cytopathology literature.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b645dad36550c631dafd465bdc046552
https://doi.org/10.1002/dc.10264
https://doi.org/10.1002/dc.10264
Publikováno v:
New-Opathies. :289-291
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b8185bde3429d573a43726eaaa52ff1
https://doi.org/10.1142/9789814355698_bmatter
https://doi.org/10.1142/9789814355698_bmatter