Zobrazeno 1 - 10
of 69
pro vyhledávání: '"FGF pathway"'
Autor:
Pingali M. Shivapriya, Anirudh Singh, Priyanshu Pandey, Nandini Chhabra, Amaresh Kumar Sahoo, Biswaranjan Paital, Pritish Kumar Varadwaj, Sintu Kumar Samanta
Publikováno v:
Frontiers in Bioscience-Landmark, Vol 26, Iss 12, Pp 1668-1678 (2021)
Small cell lung cancer (SCLC) is known for its rapid growth with high metastatic spread. Its treatment remains a major challenge for oncologists due to the high mutation rate and other clinical disadvantages. The survival rate of these patients is ve
Externí odkaz:
https://doaj.org/article/8f4e1982031d40739cd57f9944598742
Autor:
Iuliu Sbiera, Stefan Kircher, Barbara Altieri, Kerstin Lenz, Constanze Hantel, Martin Fassnacht, Silviu Sbiera, Matthias Kroiss
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Adrenocortical carcinoma (ACC) is a rare endocrine malignancy and treatment of advanced disease is challenging. Clinical trials with multi-tyrosine kinase inhibitors in the past have yielded disappointing results. Here, we investigated fibroblast gro
Externí odkaz:
https://doaj.org/article/9e83a1edfae5460297374a0abbff6473
Akademický článek
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Publikováno v:
eLife, Vol 8 (2019)
Coordinated migration of cell collectives is important during embryonic development and relies on cells integrating multiple mechanical and chemical cues. Recently, we described that focal activation of the FGF pathway promotes the migration of the p
Externí odkaz:
https://doaj.org/article/f2984a701c614690b817a4bd34d82bfa
Autor:
Virginia Albiñana, Guillermo Giménez-Gallego, Angela García-Mato, Patricia Palacios, Lucia Recio-Poveda, Angel-M Cuesta, José-Luis Patier, Luisa-María Botella
Publikováno v:
TH Open, Vol 03, Iss 03, Pp e230-e243 (2019)
Hereditary hemorrhagic telangiectasia (HHT) is a vascular dysplasia characterized by recurrent and spontaneous epistaxis (nose bleeds), telangiectases on skin and mucosa, internal organ arteriovenous malformations, and dominant autosomal inheritance.
Externí odkaz:
https://doaj.org/article/02fb504621504e31997fc759d8991017
Publikováno v:
Genes; Volume 14; Issue 4; Pages: 838
Hemifacial microsomia (HFM), a rare disorder of first- and second-pharyngeal arch development, has been linked to a point mutation in VWA1 (von Willebrand factor A domain containing 1), encoding the protein WARP in a five-generation pedigree. However
Autor:
Peter F. Renz, Daniel Spies, Panagiota Tsikrika, Anton Wutz, Tobias A. Beyer, Constance Ciaudo
Publikováno v:
Biology, Vol 9, Iss 12, p 470 (2020)
The fibroblast growth factor (FGF) and the transforming growth factor-β (TGF-β) pathways are both involved in the maintenance of human embryonic stem cells (hESCs) and regulate the onset of their differentiation. Their converging functions have sug
Externí odkaz:
https://doaj.org/article/922a131c6b584b38a2bf5ebbc370ace8
Akademický článek
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Autor:
Guillermo Giménez-Gallego, Luisa María Botella, Ángela García-Mato, José-Luis Patier, Virginia Albiñana, Angel Cuesta, Lucía Recio-Poveda, Patricia Palacios
Publikováno v:
TH Open, Vol 03, Iss 03, Pp e230-e243 (2019)
Digital.CSIC. Repositorio Institucional del CSIC
instname
TH Open: Companion Journal to Thrombosis and Haemostasis
Digital.CSIC. Repositorio Institucional del CSIC
instname
TH Open: Companion Journal to Thrombosis and Haemostasis
14 p.-8 fig.-1 tab
Hereditary hemorrhagic telangiectasia (HHT) is a vascular dysplasia characterized by recurrent and spontaneous epistaxis (nose bleeds), telangiectases on skin and mucosa, internal organ arteriovenous malformations, and dominan
Hereditary hemorrhagic telangiectasia (HHT) is a vascular dysplasia characterized by recurrent and spontaneous epistaxis (nose bleeds), telangiectases on skin and mucosa, internal organ arteriovenous malformations, and dominan
Autor:
Constance Ciaudo, Tobias A. Beyer, Panagiota Tsikrika, Peter F. Renz, Daniel Spies, Anton Wutz
Publikováno v:
Biology, Vol 9, Iss 470, p 470 (2020)
Biology, 9 (12)
Biology
Volume 9
Issue 12
Biology, 9 (12)
Biology
Volume 9
Issue 12
The fibroblast growth factor (FGF) and the transforming growth factor-&beta
(TGF-&beta
) pathways are both involved in the maintenance of human embryonic stem cells (hESCs) and regulate the onset of their differentiation. Their converging f
(TGF-&beta
) pathways are both involved in the maintenance of human embryonic stem cells (hESCs) and regulate the onset of their differentiation. Their converging f