Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Franco Felix"'
Autor:
Ann E. Collier, Samantha N. Piekos, Angela Liu, Jillian M. Pattison, Franco Felix, Alessandro A. Bailetti, Egor Sedov, Sadhana Gaddam, Hanson Zhen, Anthony E. Oro
Publikováno v:
iScience, Vol 26, Iss 3, Pp 106125- (2023)
Summary: Ectodermal dysplasias including skin abnormalities and cleft lip/palate result from improper surface ectoderm (SE) patterning. However, the connection between SE gene regulatory networks and disease remains poorly understood. Here, we dissec
Externí odkaz:
https://doaj.org/article/afe45ebf4a7949d48c0c76b1a5a59693
Autor:
Barbara Gonzalez-Teran, Maureen Pittman, Franco Felix, Reuben Thomas, Desmond Richmond-Buccola, Ruth Hüttenhain, Krishna Choudhary, Elisabetta Moroni, Mauro W. Costa, Yu Huang, Arun Padmanabhan, Michael Alexanian, Clara Youngna Lee, Bonnie E.J. Maven, Kaitlen Samse-Knapp, Sarah U. Morton, Michael McGregor, Casey A. Gifford, J.G. Seidman, Christine E. Seidman, Bruce D. Gelb, Giorgio Colombo, Bruce R. Conklin, Brian L. Black, Benoit G. Bruneau, Nevan J. Krogan, Katherine S. Pollard, Deepak Srivastava
Publikováno v:
Cell, vol 185, iss 5
Cell
Cell (Cambridge) 185 (2022): 794–814.e30. doi:10.1016/j.cell.2022.01.021
info:cnr-pdr/source/autori:Gonzalez-Teran B.; Pittman M.; Felix F.; Thomas R.; Richmond-Buccola D.; Huttenhain R.; Choudhary K.; Moroni E.; Costa M.W.; Huang Y.; Padmanabhan A.; Alexanian M.; Lee C.Y.; Maven B.E.J.; Samse-Knapp K.; Morton S.U.; McGregor M.; Gifford C.A.; Seidman J.G.; Seidman C.E.; Gelb B.D.; Colombo G.; Conklin B.R.; Black B.L.; Bruneau B.G.; Krogan N.J.; Pollard K.S.; Srivastava D./titolo:Transcription factor protein interactomes reveal genetic determinants in heart disease/doi:10.1016%2Fj.cell.2022.01.021/rivista:Cell (Cambridge)/anno:2022/pagina_da:794/pagina_a:814.e30/intervallo_pagine:794–814.e30/volume:185
Cell
Cell (Cambridge) 185 (2022): 794–814.e30. doi:10.1016/j.cell.2022.01.021
info:cnr-pdr/source/autori:Gonzalez-Teran B.; Pittman M.; Felix F.; Thomas R.; Richmond-Buccola D.; Huttenhain R.; Choudhary K.; Moroni E.; Costa M.W.; Huang Y.; Padmanabhan A.; Alexanian M.; Lee C.Y.; Maven B.E.J.; Samse-Knapp K.; Morton S.U.; McGregor M.; Gifford C.A.; Seidman J.G.; Seidman C.E.; Gelb B.D.; Colombo G.; Conklin B.R.; Black B.L.; Bruneau B.G.; Krogan N.J.; Pollard K.S.; Srivastava D./titolo:Transcription factor protein interactomes reveal genetic determinants in heart disease/doi:10.1016%2Fj.cell.2022.01.021/rivista:Cell (Cambridge)/anno:2022/pagina_da:794/pagina_a:814.e30/intervallo_pagine:794–814.e30/volume:185
Congenital heart disease (CHD) is present in 1% of live births, yet identification of causal mutations remains challenging. We hypothesized that genetic determinants for CHDs may lie in the protein interactomes of transcription factors whose mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bcdf4435eb5987a378294012ffb20d0
https://escholarship.org/uc/item/00m1b8f0
https://escholarship.org/uc/item/00m1b8f0
Autor:
Barbara Gonzalez Teran, Maureen Pittman, Reuben Thomas, Franco Felix, Desmond Richmond-Buccola, Krishna Choudhary, Elisabetta Moroni, Colombo Giorgio, Arun Padmanabhan, Mauro Costa, Yu Huang, Michael Alexanian, Clara Lee, Bonie Cole, Kaitlen Samse-Knapp, Michael McGregor, Casey Gifford, Ruth Huttenhain, Bruce Gelb, Bruce Conklin, Brian L Black, Benoit Bruneau, Nevan Krogan, Katherine Pollard, Deepak Srivastava
Publikováno v:
Circulation, vol 144, iss Suppl_1
Congenital heart disease (CHD) is present in 1% of live births, yet despite large-scale genomic sequencing efforts, identification of causal mutations remains a challenge. We hypothesized that genetic determinants for CHDs may lie in the protein inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da2adc3f664c2fdd53e234c26c9b7c74
https://escholarship.org/uc/item/2pq493zw
https://escholarship.org/uc/item/2pq493zw
Autor:
Reuben Thomas, Desmond Richmond-Buccola, Ruth Hüttenhain, Bruce D. Gelb, Elisabetta Moroni, Giorgio Colombo, Casey A. Gifford, Nevan J. Krogan, Deepak Srivastava, Kaitlen Samse-Knapp, Brian L. Black, Bonnie Cole, Franco Felix, Michael Alexanian, Bárbara González-Terán, Benoit G. Bruneau, Katherine S. Pollard, Maureen Pittman, Michael McGregor, Bruce R. Conklin, Krishna Choudhary
SUMMARYCongenital heart disease (CHD) is present in 1% of live births, yet identification of causal mutations remains a challenge despite large-scale genomic sequencing efforts. We hypothesized that genetic determinants for CHDs may lie in protein in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08cb514f7b4ca318bf306b2c3b24e86a
https://doi.org/10.1101/2021.01.05.423837
https://doi.org/10.1101/2021.01.05.423837
Autor:
Elielton Franco Felix, Fernanda da Silva Barbosa Paz, Aulisângela da Silva Queiroz, Joab de Souza Arouche
Publikováno v:
Tópicos em Fonoaudiologia I: dados literários sobre a fonoaudiologia e algumas de suas áreas de atuação ISBN: 9786580476879
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9b681f656659a7fe3609199d1aaa9ae
https://doi.org/10.36926/editorainovar-978-65-80476-87_014
https://doi.org/10.36926/editorainovar-978-65-80476-87_014
Autor:
Parisha P. Shah, Arun Padmanabhan, Franco Felix, Ricardo Linares-Saldana, Rajan Jain, Andrew J. Connolly, Qiming Duan, Michael Alexanian, Qiaohong Wang, Wonho Kim, Saptarsi M. Haldar, Austin Hsu, Gaia Andreoletti, Yu Huang, Sarah A. B. Winchester, Juan A. Perez-Bermejo, Bárbara González-Terán, Li Li, Deepak Srivastava
Publikováno v:
Circulation, vol 142, iss 24
Background: Gene regulatory networks control tissue homeostasis and disease progression in a cell type–specific manner. Ubiquitously expressed chromatin regulators modulate these networks, yet the mechanisms governing how tissue specificity of thei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d2f901da1e37ad46432723db6cc69f5
https://escholarship.org/uc/item/9592f6t2
https://escholarship.org/uc/item/9592f6t2
Autor:
Arun Padmanabhan, Katherine S. Pollard, Joshua G. Travers, Ricardo Linares-Saldana, Kathryn N. Ivey, Pawel F. Przytycki, Jin Yang, Michael G. Rosenfeld, Barbara Gonzalez Teran, Franco Felix, Gaia Andreoletti, Qiming Duan, Deepak Srivastava, Michael Alexanian, Rudi Micheletti, Sanjeev S. Ranade, Saptarsi M. Haldar, Lin Ye, Yu Huang, Casey A. Gifford, Rajan Jain, Timothy A. McKinsey
In diseased organs, stress-activated signaling cascades alter chromatin, triggering broad shifts in transcription and cell state that exacerbate pathology. Fibroblast activation is a common stress response that worsens lung, liver, kidney and heart d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f822752ed23f4eccecada4498b5950e0
https://doi.org/10.1101/2020.07.21.214874
https://doi.org/10.1101/2020.07.21.214874
Autor:
Rajan Jain, Ricardo Linares-Saldana, Rudi Micheletti, Pawel F. Przytycki, Arun Padmanabhan, Katherine S. Pollard, Sanjeev S. Ranade, Lin Ye, Li Li, Ana C. Silva, Bárbara González-Terán, Angelo Pelonero, Qiming Duan, Saptarsi M. Haldar, Nandhini Sadagopan, Joshua G. Travers, Michael Alexanian, Deepak Srivastava, Clara Youngna Lee, Franco Felix, Michael G. Rosenfeld, Gaia Andreoletti, Timothy A. McKinsey, Yu Huang, Casey A. Gifford
Publikováno v:
Signal Transduction and Targeted Therapy
Nature
Nature, vol 595, iss 7867
Nature
Nature, vol 595, iss 7867
In diseased organs, stress-activated signalling cascades alter chromatin, thereby triggering maladaptive cell state transitions. Fibroblast activation is a common stress response in tissues that worsens lung, liver, kidney and heart disease, yet its
Autor:
Franco Felix, Casey A. Gifford, Kaitlen Samse-Knapp, Elisabetta Moroni, Bonnie Cole, Michael Alexanian, Maureen Pittman, Bruce D. Gelb, Deepak Srivastava, Benoit G. Bruneau, Michael McGregor, Bruce R. Conklin, Bárbara González-Terán, Ruth Hüttenhain, Giorgio Colombo, Katherine S. Pollard, Desmond Richmond-Buccola, Krishna Choudhary, Nevan J. Krogan, Brian L. Black, Reuben Thomas
Publikováno v:
SSRN Electronic Journal.
Congenital heart disease (CHD) is present in 1% of live births, yet identification of causal mutations remains a challenge despite large-scale genomic sequencing efforts. We hypothesized that genetic determinants for CHDs may lie in protein interacto
Autor:
Franco Félix
Maten a Darwin es una desmesurada selva narrativa, desquiciadamente minuciosa y total. Los descendientes de Charles Darwin están obsesionados con encontrar la fórmula de la vida eterna. Sin embargo, y paradójicamente, al ser el resultado de una un