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Results for
""Smad3 Protein""[mesh_terms]

17 Results

Searching titles within these results

Clinical and genetic data of 22 new patients with SMAD3 pathogenic variants and review of the literature.

Bertrand Chesneau, Thomas Edouard, Yves Dulac, Hélène Colineaux, Maud Langeois, Nadine Hanna, Catherine Boileau, Pauline Arnaud, Nicolas Chassaing, Sophie Julia, Guillaume Jondeau, Aurélie Plancke, Philippe Khau Van Kien, Julie Plaisancié

Molecular genetics & genomic medicine 2021;8(5):e1132

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Novel SMAD3 p.Arg386Thr genetic variant co-segregating with thoracic aortic aneurysm and dissection.

Karolina Engström, Farkas Vánky, Malin Rehnberg, Cecilia Trinks, Jon Jonasson, Anna Green, Cecilia Gunnarsson

Molecular genetics & genomic medicine 2021;8(4):e1089

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Biochemical studies and molecular dynamics simulations of Smad3-Erbin interaction identify a non-classical Erbin PDZ binding.

Nadine Déliot, Matthieu Chavent, Claire Nourry, Patrick Lécine, Camille Arnaud, Aurélie Hermant, Bernard Maigret, Jean-Paul Borg

Biochemical and biophysical research communications 2009;378(3):360-5

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Unravelling the transcriptional responses of TGF-β: Smad3 and EZH2 constitute a regulatory switch that controls neuroretinal epithelial cell fate specification.

Darrell Andrews, Giorgio Oliviero, Letizia De Chiara, Ariane Watson, Emily Rochford, Kieran Wynne, Ciaran Kennedy, Shane Clerkin, Benjamin Doyle, Catherine Godson, Paul Connell, Colm O'Brien, Gerard Cagney, John Crean

FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2020;33(5):6667-6681

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Inhibition of Smad antiproliferative function by CDK phosphorylation.

Fang Liu, Isao Matsuura

Cell cycle (Georgetown, Tex.) 2006;4(1):63-6

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Genotypic Categorization of Loeys-Dietz Syndrome Based on 24 Novel Families and Literature Data.

Letizia Camerota, Marco Ritelli, Anita Wischmeijer, Silvia Majore, Valeria Cinquina, Paola Fortugno, Rosanna Monetta, Laura Gigante, Federica Carla Sangiuolo, Giuseppe Novelli, Marina Colombi, Francesco Brancati

Genes 2020;10(10):764

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The genetic architecture of hip shape and its role in the development of hip osteoarthritis and fracture.

Richard M Aspden, Jennifer S Gregory, Rhona Beynon, Huandong Lin, John P Kemp, Monika Frysz, Xin Gao, Fiona R Saunders, George Davey Smith, Jonathan H Tobias, David M Evans, Sijia Wang, Nicholas C Harvey, Benjamin G Faber, Jaiyi Zheng, Kaitlyn A Flynn, Raja Ebsim, Claudia Lindner, Timothy Cootes

Human molecular genetics 2025;34(3):207-217

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Clinical Exome Sequencing as a Novel Tool for Diagnosing Loeys-Dietz Syndrome Type 3.

A Blinc, A Maver, G Rudolf, J Tasič, J Pretnar Oblak, P Berden, B Peterlin

European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery 2016;50(6):816-21

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Genetic variants underlying vitamin D metabolism and VDR-TGFβ-1-SMAD3 interaction may impact on HCV progression: a study based on dbGaP data from the HALT-C study.

Laura A de Azevedo, Ursula Matte, Themis R da Silveira, Mário R Álvares-da-Silva

Journal of human genetics 2018;62(11):969-977

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DNA methylation map in circulating leukocytes mirrors subcutaneous adipose tissue methylation pattern: a genome-wide analysis from non-obese and obese patients.

A B Crujeiras, A Diaz-Lagares, J Sandoval, F I Milagro, S Navas-Carretero, M C Carreira, A Gomez, D Hervas, M P Monteiro, F F Casanueva, M Esteller, J A Martinez

Scientific reports 2018;7():41903

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Inflammation-related signaling pathways implicating TGFβ are revealed in the expression profiling of MCF7 cell treated with fermented soybean, chungkookjang.

Jae Sung Hwang, Hyung Jae Yoo, Hye Jung Song, Kyu Kwang Kim, Young Jin Chun, Toshiro Matsui, Han Bok Kim

Nutrition and cancer 2011;63(4):645-52

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Bifidobacterium breve enhances transforming growth factor beta1 signaling by regulating Smad7 expression in preterm infants.

Tohru Fujii, Yoshikazu Ohtsuka, Tsubasa Lee, Takahiro Kudo, Hiromichi Shoji, Hiroaki Sato, Satoru Nagata, Toshiaki Shimizu, Yuichiro Yamashiro

Journal of pediatric gastroenterology and nutrition 2007;43(1):83-8

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Fine-mapping inflammatory bowel disease loci to single-variant resolution.

Hailiang Huang, Ming Fang, Luke Jostins, Maša Umićević Mirkov, Gabrielle Boucher, Carl A Anderson, Vibeke Andersen, Isabelle Cleynen, Adrian Cortes, François Crins, Mauro D'Amato, Valérie Deffontaine, Julia Dmitrieva, Elisa Docampo, Mahmoud Elansary, Kyle Kai-How Farh, Andre Franke, Ann-Stephan Gori, Philippe Goyette, Jonas Halfvarson, Talin Haritunians, Jo Knight, Ian C Lawrance, Charlie W Lees, Edouard Louis, Rob Mariman, Theo Meuwissen, Myriam Mni, Yukihide Momozawa, Miles Parkes, Sarah L Spain, Emilie Théâtre, Gosia Trynka, Jack Satsangi, Suzanne van Sommeren, Severine Vermeire, Ramnik J Xavier, Rinse K Weersma, Richard H Duerr, Christopher G Mathew, John D Rioux, Dermot P B McGovern, Judy H Cho, Michel Georges, Mark J Daly, Jeffrey C Barrett

Nature 2017;547(7662):173-178

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Inhaled corticosteroid normalizes some but not all airway vascular remodeling in COPD.

Amir Soltani, Eugene Haydn Walters, David W Reid, Shakti Dhar Shukla, Kaosia Nowrin, Chris Ward, H Konrad Muller, Sukhwinder Singh Sohal

International journal of chronic obstructive pulmonary disease 2017;11():2359-2367

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Non-syndromic thoracic aortic aneurysms and dissections--a genetic review.

Pengyu Zhang, Eryong Zhang, Jingxiu Fan, Jun Gu

Frontiers in bioscience (Landmark edition) 2013;18(1):305-11

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Results: 1 – 15 / 17

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Results for ""Smad3 Protein""[mesh_terms]

Clinical and genetic data of 22 new patients with SMAD3 pathogenic variants and review of the literature.

Novel SMAD3 p.Arg386Thr genetic variant co-segregating with thoracic aortic aneurysm and dissection.

Biochemical studies and molecular dynamics simulations of Smad3-Erbin interaction identify a non-classical Erbin PDZ binding.

Unravelling the transcriptional responses of TGF-β: Smad3 and EZH2 constitute a regulatory switch that controls neuroretinal epithelial cell fate specification.

Inhibition of Smad antiproliferative function by CDK phosphorylation.

Genotypic Categorization of Loeys-Dietz Syndrome Based on 24 Novel Families and Literature Data.

The genetic architecture of hip shape and its role in the development of hip osteoarthritis and fracture.

Clinical Exome Sequencing as a Novel Tool for Diagnosing Loeys-Dietz Syndrome Type 3.

Genetic variants underlying vitamin D metabolism and VDR-TGFβ-1-SMAD3 interaction may impact on HCV progression: a study based on dbGaP data from the HALT-C study.

DNA methylation map in circulating leukocytes mirrors subcutaneous adipose tissue methylation pattern: a genome-wide analysis from non-obese and obese patients.

Inflammation-related signaling pathways implicating TGFβ are revealed in the expression profiling of MCF7 cell treated with fermented soybean, chungkookjang.

Bifidobacterium breve enhances transforming growth factor beta1 signaling by regulating Smad7 expression in preterm infants.

Fine-mapping inflammatory bowel disease loci to single-variant resolution.

Inhaled corticosteroid normalizes some but not all airway vascular remodeling in COPD.

Non-syndromic thoracic aortic aneurysms and dissections--a genetic review.

Results for
""Smad3 Protein""[mesh_terms]