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Results for

""Receptor, Transforming Growth Factor-beta Type II""[mesh_terms]

16 Results

Searching titles within these results

Arterial tortuosity in pediatric Loeys-Dietz syndrome patients.

Laia Brunet-Garcia, Pirasuja Prabaharan, Luc Bruyndonckx, Ella Field, Felice D'Arco, Claudio Capelli, Elena Cervi

American journal of medical genetics. Part A 2024;194(3):e63465

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Neonatal presentation of Loeys-Dietz syndrome: two case reports and review of the literature.

Laura Travan, Luigi Memo, Yasmin Al Naber, Flavio Faletra, Agnese Feresin, Laura Morra, Francesco Baldo

Italian journal of pediatrics 2022;48(1):85

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Arthrogryposis as neonatal presentation of Loeys-Dietz syndrome due to a novel TGFBR2 mutation.

Eduardo F Tizzano, Teresa Vendrell, Gemma Giralt, Angel Sanchez-Montanez, Paula Fernández-Alvarez, Irene Valenzuela, Francina Munell

European journal of medical genetics 2017;60(6):303-307

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Dysmorphology.

Alexander Youngjoon Kim, Joann Norma Bodurtha

Pediatrics in review 2020;40(12):609-618

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

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

Genes 2020;10(10):764

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Functional validation reveals the novel missense V419L variant in associated with Loeys-Dietz syndrome (LDS) impairs canonical TGF-β signaling.

Margot A Cousin, Michael T Zimmermann, Angela J Mathison, Patrick R Blackburn, Nicole J Boczek, Gavin R Oliver, Gwen A Lomberk, Raul A Urrutia, David R Deyle, Eric W Klee

Cold Spring Harbor molecular case studies 2017;3(4):a001727

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Arterial tortuosity in genetic arteriopathies.

Shaine A Morris

Current opinion in cardiology 2016;30(6):587-93

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Transforming growth factor-β signalling: role and consequences of Smad linker region phosphorylation.

Narin Osman, Peter J Little, Wenhua Zheng, Suowen Xu, Muhamad Ashraf Rostam, Hossein Babaahmadi Rezaei, Micah L Burch, Danielle Kamato, Terrence J Piva

Cellular signalling 2014;25(10):2017-24

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A new sporadic case of early-onset Loeys-Dietz syndrome due to the recurrent mutation p.R528C in the TGFBR2 gene substantiates interindividual clinical variability.

A Jamsheer, C Henggeler, J Wierzba, B Loeys, A De Paepe, Ch Stheneur, A Latos-Bielenska, G Matyas, N Badziag, K Matuszewska

Journal of applied genetics 2010;50(4):405-10

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The Role of Th17/Treg Axis in the Traditional Chinese Medicine Intervention on Immune-Mediated Inflammatory Diseases: A Systematic Review.

Yong-Yue Xu, Dong-Mei Wang, Hua-Sheng Liang, Ze-Hao Liu, Jun-Xia Li, Mao-Jie Wang, Xiu-Min Chen, Deepak M W Balak, Timothy R D J Radstake, Run-Yue Huang, Chuan-Jian Lu

The American journal of Chinese medicine 2020;48(3):535-558

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Localization of recognition site between transforming growth factor-beta1 (TGF-beta1) and TGF beta receptor type II: possible implications in breast cancer.

V Ivanović, M Demajo, N Todorović-Raković, D Nikolić-Vukosavljević, Z Nesković-Konstantinović, K Krtolica, V Veljković, J Prljić, B Dimitrijević

Medical hypotheses 2004;62(5):727-32

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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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Rapamycin induces the fusion-type independent downregulation of the EWS/FLI-1 proteins and inhibits Ewing's sarcoma cell proliferation.

Silvia Mateo-Lozano, Oscar M Tirado, Vicente Notario

Oncogene 2004;22(58):9282-7

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Genetic basis of hereditary thoracic aortic aneurysms and dissections.

Issei Komuro, Norifumi Takeda

Journal of cardiology 2020;74(2):136-143

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Loeys-Dietz syndrome.

Lut Van Laer, Harry Dietz, Bart Loeys

Advances in experimental medicine and biology 2014;802():95-105

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Results: 1 – 15 / 16

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Results for ""Receptor, Transforming Growth Factor-beta Type II""[mesh_terms]

Arterial tortuosity in pediatric Loeys-Dietz syndrome patients.

Neonatal presentation of Loeys-Dietz syndrome: two case reports and review of the literature.

Arthrogryposis as neonatal presentation of Loeys-Dietz syndrome due to a novel TGFBR2 mutation.

Dysmorphology.

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

Functional validation reveals the novel missense V419L variant in associated with Loeys-Dietz syndrome (LDS) impairs canonical TGF-β signaling.

Arterial tortuosity in genetic arteriopathies.

Transforming growth factor-β signalling: role and consequences of Smad linker region phosphorylation.

A new sporadic case of early-onset Loeys-Dietz syndrome due to the recurrent mutation p.R528C in the TGFBR2 gene substantiates interindividual clinical variability.

The Role of Th17/Treg Axis in the Traditional Chinese Medicine Intervention on Immune-Mediated Inflammatory Diseases: A Systematic Review.

Localization of recognition site between transforming growth factor-beta1 (TGF-beta1) and TGF beta receptor type II: possible implications in breast cancer.

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

Rapamycin induces the fusion-type independent downregulation of the EWS/FLI-1 proteins and inhibits Ewing's sarcoma cell proliferation.

Genetic basis of hereditary thoracic aortic aneurysms and dissections.

Loeys-Dietz syndrome.

Results for

""Receptor, Transforming Growth Factor-beta Type II""[mesh_terms]