Tumor Necrosis Factor-alpha < Tumor Suppressor Proteins < Tumor Virus Infections

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List of bibliographic references

Number of relevant bibliographic references: 45.
[0-20] [0 - 20][0 - 45][20-40]

Ident.	Authors (with country if any)	Title
000104 (2017)	Francoise Pujol [Suède] ; Tina Hodgson [Suède] ; Ines Martinez-Corral [Suède] ; Anne-Catherine Prats [Suède] ; Danelle Devenport [Suède] ; Masatoshi Takeichi [Suède] ; Elisabeth Genot [Suède] ; Taija M Kinen [Suède] ; Philippa Francis-West [Suède] ; Barbara Garmy-Susini [Suède] ; Florence Tatin [France]	Dachsous1-Fat4 Signaling Controls Endothelial Cell Polarization During Lymphatic Valve Morphogenesis-Brief Report.
000423 (2017)	André Viveiros [Autriche] ; Marion Reiterer [Autriche] ; Benedikt Schaefer [Autriche] ; Armin Finkenstedt [Autriche] ; Stefan Schneeberger [Autriche] ; Hubert Schwaighofer [Autriche] ; Patrizia Moser [Autriche] ; Rudolf Sprenger [Autriche] ; Bernhard Glodny [Autriche] ; Wolfgang Vogel [Autriche] ; Andreas R. Janecke [Autriche] ; Heinz Zoller [Autriche]	CCBE1 mutation causing sclerosing cholangitis: Expanding the spectrum of lymphedema-cholestasis syndrome.
000433 (2017)	Garry Cooper	Genetics and lymphoedema: a future yet to be fully discovered.
000439 (2017)	Daisuke Iwasaki ; Yuhei Yamamoto ; Naoki Murao ; Akihiko Oyama ; Emi Funayama ; Hiroshi Furukawa	Establishment of an Acquired Lymphedema Model in the Mouse Hindlimb: Technical Refinement and Molecular Characteristics.
000A96 (2016)	Carolyn C. Jackson [États-Unis] ; Lucy Best [États-Unis] ; Lazaro Lorenzo [France] ; Jean-Laurent Casanova [États-Unis] ; Jochen Wacker [Allemagne] ; Simone Bertz [Allemagne] ; Abbas Agaimy [Allemagne] ; Thomas Harrer [Allemagne]	A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression.
000D50 (2015)	Jan Kazenwadel ; Kelly L. Betterman ; Chan-Eng Chong ; Philippa H. Stokes ; Young K. Lee ; Genevieve A. Secker ; Yan Agalarov ; Cansaran Saygili Demir ; David M. Lawrence ; Drew L. Sutton ; Sebastien P. Tabruyn ; Naoyuki Miura ; Marjo Salminen ; Tatiana V. Petrova ; Jacqueline M. Matthews ; Christopher N. Hahn ; Hamish S. Scott ; Natasha L. Harvey	GATA2 is required for lymphatic vessel valve development and maintenance.
000F12 (2015)	Sarah F. Pollack [États-Unis] ; Alexandra L. Geffrey [États-Unis] ; Elizabeth A. Thiele [États-Unis] ; Uzma Shah [États-Unis]	Primary intestinal lymphangiectasia treated with rapamycin in a child with tuberous sclerosis complex (TSC).
000F16 (2015)	Patrick Frosk [Canada] ; Bernard Chodirker [Canada] ; Louise Simard [Canada] ; Wael El-Matary [Canada] ; Ana Hanlon-Dearman [Canada] ; Jeremy Schwartzentruber [Canada] ; Jacek Majewski [Canada] ; Cheryl Rockman-Greenberg [Canada]	A novel CCBE1 mutation leading to a mild form of hennekam syndrome: case report and review of the literature.
000F58 (2015)	M Guy Roukens ; Josi Peterson-Maduro ; Yvonne Padberg ; Michael Jeltsch ; Veli-Matti Lepp Nen ; Frank L. Bos ; Kari Alitalo ; Stefan Schulte-Merker ; Dörte Schulte [Allemagne]	Functional Dissection of the CCBE1 Protein: A Crucial Requirement for the Collagen Repeat Domain.
001248 (2015)	Shuqun Qi [République populaire de Chine] ; Jian Pan	Cell-based therapy for therapeutic lymphangiogenesis.
001382 (2014)	Pengchun Yu [États-Unis] ; Joe K. Tung [États-Unis] ; Michael Simons [États-Unis]	Lymphatic fate specification: an ERK-controlled transcriptional program.
001494 (2014)	Mariëlle Alders [Pays-Bas] ; Lihadh Al-Gazali ; Isabelle Cordeiro ; Bruno Dallapiccola ; Livia Garavelli ; Beyhan Tuysuz ; Faranak Salehi ; Martin A. Haagmans ; Olaf R. Mook ; Charles B. Majoie ; Marcel M. Mannens ; Raoul C. Hennekam	Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome.
001599 (2014)	Alexandra L. Geffrey [États-Unis] ; Julianna E. Shinnick ; Brigid A. Staley ; Susana Boronat ; Elizabeth A. Thiele	Lymphedema in tuberous sclerosis complex.
001669 (2014)	Michael Jeltsch [Finlande] ; Sawan Kumar Jha ; Denis Tvorogov ; Andrey Anisimov ; Veli-Matti Lepp Nen ; Tanja Holopainen ; Riikka Kivel ; Sagrario Ortega ; Terhi K Rpanen ; Kari Alitalo	CCBE1 enhances lymphangiogenesis via A disintegrin and metalloprotease with thrombospondin motifs-3-mediated vascular endothelial growth factor-C activation.
001811 (2014)	Andreas Van Impel [Pays-Bas] ; Stefan Schulte-Merker	A fisheye view on lymphangiogenesis.
001815 (2014)	Ying Yang [États-Unis] ; Guillermo Oliver	Transcriptional control of lymphatic endothelial cell type specification.
001898 (2013)	Sohela Shah [États-Unis] ; Laura K. Conlin ; Luis Gomez ; Ystein Aagenaes ; Kristin Eiklid ; A S Knisely ; Michael T. Mennuti ; Randolph P. Matthews ; Nancy B. Spinner ; Laura N. Bull	CCBE1 mutation in two siblings, one manifesting lymphedema-cholestasis syndrome, and the other, fetal hydrops.
001915 (2013)	Lucy A. Truman [États-Unis] ; Noelia A-Gonzalez ; Kevin L. Bentley ; Nancy H. Ruddle	Lymphatic vessel function in head and neck inflammation.
001982 (2013)	Michael Simons [États-Unis] ; Anne Eichmann	Physiology. Lymphatics are in my veins.
001A04 (2013)	Nanhang Lu [République populaire de Chine] ; Yong Zhang ; Zihao Feng ; Fazhi Qi	[A preliminary study on vascular endothelial growth factor C gene modified lymph node transplantation in promoting proliferation of lymphatic endothelial cells].
001C94 (2013)	Zhiying Zou [États-Unis] ; David R. Enis ; Hung Bui ; Eugene Khandros ; Vinayak Kumar ; Zoltan Jakus ; Christopher Thom ; Yiqing Yang ; Veerpal Dhillon ; Mei Chen ; Minmin Lu ; Mitchell J. Weiss ; Mark L. Kahn	The secreted lymphangiogenic factor CCBE1 is essential for fetal liver erythropoiesis.

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