Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Esko A Kautto"'
Autor:
Kathleen M. Schieffer, Alexander Z. Feldman, Esko A. Kautto, Sean McGrath, Anthony R. Miller, Maria Elena Hernandez-Gonzalez, Stephanie LaHaye, Katherine E. Miller, Daniel C. Koboldt, Patrick Brennan, Benjamin Kelly, Amy Wetzel, Vibhuti Agarwal, Margaret Shatara, Suzanne Conley, Diana P. Rodriguez, Rolla Abu-Arja, Ala Shaikhkhalil, Matija Snuderl, Brent A. Orr, Jonathan L. Finlay, Diana S. Osorio, Annie I. Drapeau, Jeffrey R. Leonard, Christopher R. Pierson, Peter White, Vincent Magrini, Elaine R. Mardis, Richard K. Wilson, Catherine E. Cottrell, Daniel R. Boué
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-11 (2021)
Abstract Retinoblastoma is a childhood cancer of the retina involving germline or somatic alterations of the RB Transcriptional Corepressor 1 gene, RB1. Rare cases of sellar-suprasellar region retinoblastoma without evidence of ocular or pineal tumor
Externí odkaz:
https://doaj.org/article/85b8e7d1df914feb8bd8c86c7a9bff75
Autor:
Christopher C. Coss, Mohamed H. Abdel-Rahman, Sameera Ezzat, Esko A. Kautto, James S. Blachly, Anees M. Dauki
This file contains supplementary figures 1-8.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4537db4dd29300625bed7da97b1f3694
https://doi.org/10.1158/0008-5472.22425256.v1
https://doi.org/10.1158/0008-5472.22425256.v1
Autor:
Christopher C. Coss, Mohamed H. Abdel-Rahman, Sameera Ezzat, Esko A. Kautto, James S. Blachly, Anees M. Dauki
Owing to the marked sexual dimorphism of hepatocellular carcinoma (HCC), sex hormone receptor signaling has been implicated in numerous aspects of liver cancer pathogenesis. We sought to reconcile the clear contribution of androgen receptor (AR) acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::115e4238e91716c4ebcf5427f8a03234
https://doi.org/10.1158/0008-5472.c.6511978
https://doi.org/10.1158/0008-5472.c.6511978
Autor:
Christopher C. Coss, Mohamed H. Abdel-Rahman, Sameera Ezzat, Esko A. Kautto, James S. Blachly, Anees M. Dauki
These tables contain relevant patient characteristics, primer sequence information for RT-PCR, whole genome sequencing read statistics, and a tabulation of DEGS from publicly available HCC cell RNA-seq data.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17afa5974ac4f70953a1b376b43eea68
https://doi.org/10.1158/0008-5472.22425259
https://doi.org/10.1158/0008-5472.22425259
Autor:
Esko A, Kautto, Kathleen M, Schieffer, Sean, McGrath, Anthony R, Miller, Maria Elena, Hernandez-Gonzalez, Samantha, Choi, Miriam R, Conces, Esteban, Fernandez-Faith, Mai-Lan, Ho, Kristy, Lee, Anna P, Lillis, Gregory D, Pearson, Stephen G, Kaler, Richard K, Wilson, Elaine R, Mardis, Vincent, Magrini, Jeffrey, Leonard, Catherine E, Cottrell
Publikováno v:
Cold Spring Harbor molecular case studies. 8(2)
Closed spinal dysraphism (SD) is a type of neural tube defect originating during early embryonic development whereby the neural tissue of the spinal defect remains covered by skin, often coinciding with markers of cutaneous stigmata. It is hypothesiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e01ed2f7ce09268dc0ed462075856316
https://pubmed.ncbi.nlm.nih.gov/35149534
https://pubmed.ncbi.nlm.nih.gov/35149534
Autor:
Daniel C. Koboldt, Maria Elena Hernandez-Gonzalez, Vincent Magrini, Peter White, Julie Balch Samora, Theresa Mihalic Mosher, Samuel J Franklin, Sean McGrath, Kim L. McBride, Marilena Melas, Ruthann B. Pfau, Richard K. Wilson, Esko A. Kautto, Mari Mori
Publikováno v:
Human mutationREFERENCES. 43(2)
Synpolydactyly 1 (SPD; MIM# 186000), also called syndactyly type II (SDTY2), is a genetic limb malformation characterized by polydactyly with syndactyly involving the webbing of the third and fourth fingers, and the fourth and fifth toes. It is cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::055a2c598febf55e3d7ab3bec4e4a35a
https://pubmed.ncbi.nlm.nih.gov/34859533
https://pubmed.ncbi.nlm.nih.gov/34859533
Autor:
Sherri Z. Millis, Amanda E. Toland, John L. Hays, Christian F. Meyer, James L. Chen, Nathan D. Seligson, Esko A. Kautto, Colin W. Stets, Edward N. Passen
Publikováno v:
The Oncologist. 24:973-979
Background Soft-tissue sarcomas (STS) describe a heterogeneous group of mesenchymal tumors with limited treatment options. Targeted therapies exist for BRCA1/2 gene alterations, but their prevalence and role have not been fully described in STS. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be2315056d9d737b7b7d9741f3dcc4e5
https://doi.org/10.1634/theoncologist.2018-0448
https://doi.org/10.1634/theoncologist.2018-0448
Autor:
Alexander Z. Feldman, Jeffrey R. Leonard, Catherine E. Cottrell, Brent A. Orr, Peter White, Ala K. Shaikhkhalil, Amy Wetzel, Rolla Abu-Arja, Vibhuti Agarwal, Jonathan L. Finlay, Diana S Osorio, Richard K. Wilson, Annie I. Drapeau, Christopher R. Pierson, Sean McGrath, Stephanie LaHaye, Daniel C. Koboldt, Katherine E. Miller, Diana P Rodriguez, Matija Snuderl, Patrick J. Brennan, Kathleen M. Schieffer, Esko A. Kautto, Elaine R. Mardis, Maria Elena Hernandez-Gonzalez, Margaret Shatara, Vincent Magrini, Benjamin J. Kelly, Suzanne Conley, Anthony R. Miller, Daniel R. Boue
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-11 (2021)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Retinoblastoma is a childhood cancer of the retina involving germline or somatic alterations of the RB Transcriptional Corepressor 1 gene, RB1. Rare cases of sellar-suprasellar region retinoblastoma without evidence of ocular or pineal tumors have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ce215653b77265a80b41866077407cc
https://pubmed.ncbi.nlm.nih.gov/33827698
https://pubmed.ncbi.nlm.nih.gov/33827698
Autor:
Charles Thomas Gregory, James S. Blachly, Esko A. Kautto, Jennifer A. Woyach, Apollinaire Ngankeu, John C. Byrd, Shelley Orwick
Publikováno v:
Nar Genomics and Bioinformatics
High-throughput short-read sequencing relies on fragmented DNA for optimal sampling of input nucleic acid. Several vendors now offer proprietary enzyme cocktails as a cheaper and more streamlined method of fragmentation when compared to acoustic shea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b2aba60098482ea475268943ae52917
Autor:
Esko A Kautto, Kathleen M Schieffer, Sean McGrath, Anthony R Miller, Maria Elena Hernandez Gonzalez, Samantha Choi, Miriam R Conces, Esteban Fernandez-Faith, Mai-Lan Ho, Kristy Lee, Anna P Lillis, Gregory D Pearson, Stephen G Kaler, Richard K Wilson, Elaine R Mardis, Vincent Magrini, Jeffrey Leonard, Catherine E Cottrell
Publikováno v:
Molecular Case Studies. :mcs.a006174
Closed spinal dysraphism (SD) is a type of neural tube defect originating during early embryonic development whereby the neural tissue of the spinal defect remains covered by skin, often coinciding with markers of cutaneous stigmata. It is hypothesiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2620ad0a5150db2803886011e4974327
https://doi.org/10.1101/mcs.a006174
https://doi.org/10.1101/mcs.a006174