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Results for
""Latent TGF-beta Binding Proteins""[mesh_terms]

6 Results

Searching titles within these results

Weill-Marchesani syndrome: natural history and genotype-phenotype correlations from 18 news cases and review of literature.

Pauline Marzin, Klaus Dieterich, Gianmaria Miolo, Valerie Cormier-Daire, Caroline Michot, Massimiliano Rossi, Christine Francannet, Sophie Rondeau, Carine le Goff, Matthieu P Robert, Jean-Luc Alessandri, Clémentine Mahaut, Céline Huber, Jean-Philippe Jaïs, Julien Van-Gils, Oana Moldovan, Sandra Mercier

Journal of medical genetics 2024;61(2):109-116

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First report of a short in-frame biallelic deletion removing part of the EGF-like domain calcium-binding motif in LTBP4 and causing autosomal recessive cutis laxa type 1C.

Margot Comel, Jean-Marie Ravel, Marion Wandzel, Myriam Bronner, Aurélie Tatopoulos, Mathilde Renaud, Laëtitia Lambert, Anne-Claire Bursztejn, Céline Bonnet

American journal of medical genetics. Part A 2022;188(11):3343-3349

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Evolution of distinct EGF domains with specific functions.

Merridee A Wouters, Isidore Rigoutsos, Carmen K Chu, Lina L Feng, Duncan B Sparrow, Sally L Dunwoodie

Protein science : a publication of the Protein Society 2005;14(4):1091-103

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Identification of the thiol isomerase-binding peptide, mastoparan, as a novel inhibitor of shear-induced transforming growth factor β1 (TGF-β1) activation.

Barry S Coller, Teresa M Brophy, Jasimuddin Ahamed

The Journal of biological chemistry 2013;288(15):10628-39

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Sphingosine kinase 1 isoform-specific interactions in breast cancer.

Daniel Yagoub, Marc R Wilkins, Angelina J Lay, Dominik C Kaczorowski, Diana Hatoum, Sarah Bajan, Gyorgy Hutvagner, Jack H Lai, Wengen Wu, Rosetta Martiniello-Wilks, Pu Xia, Eileen M McGowan

Molecular endocrinology (Baltimore, Md.) 2015;28(11):1899-915

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Syndromic and non-syndromic aneurysms of the human ascending aorta share activation of the Smad2 pathway.

Delphine Gomez, Ayman Al Haj Zen, Luciano F Borges, Monique Philippe, Paulo Sampaio Gutierrez, Guillaume Jondeau, Jean-Baptiste Michel, Roger Vranckx

The Journal of pathology 2009;218(1):131-42

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Results: 1 – 6 / 6

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Results for ""Latent TGF-beta Binding Proteins""[mesh_terms]

Weill-Marchesani syndrome: natural history and genotype-phenotype correlations from 18 news cases and review of literature.

First report of a short in-frame biallelic deletion removing part of the EGF-like domain calcium-binding motif in LTBP4 and causing autosomal recessive cutis laxa type 1C.

Evolution of distinct EGF domains with specific functions.

Identification of the thiol isomerase-binding peptide, mastoparan, as a novel inhibitor of shear-induced transforming growth factor β1 (TGF-β1) activation.

Sphingosine kinase 1 isoform-specific interactions in breast cancer.

Syndromic and non-syndromic aneurysms of the human ascending aorta share activation of the Smad2 pathway.

Results for
""Latent TGF-beta Binding Proteins""[mesh_terms]