Ngā hua rapu kaituhi :: APM

1

Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect mā Pascal Brouillard

I whakaputaina 2005

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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2

Genetics of lymphatic anomalies mā Pascal Brouillard, Laurence M. Boon, Miikka Vikkula

I whakaputaina 2014

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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3

Loss of ADAMTS3 activity causes Hennekam lymphangiectasia–lymphedema syndrome 3 mā Pascal Brouillard, Laura Dupont, Raphaël Helaers, Richard Coulie, George E. Tiller, Joseph Peeden, Alain Colige, Miikka Vikkula

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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4

Efficient activation of the lymphangiogenic growth factor VEGF-C requires the C-terminal domain of VEGF-C and the N-terminal domain of CCBE1 mā Sawan Kumar Jha, Khushbu Rauniyar, Terhi Kärpänen, Veli‐Matti Leppänen, Pascal Brouillard, Miikka Vikkula, Kari Alitalo, Michael Jeltsch

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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5

KRAS-driven model of Gorham-Stout disease effectively treated with trametinib mā Nassim Homayun Sepehr, Anna McCarter, Raphaël Helaers, Christine Galant, Laurence M. Boon, Pascal Brouillard, Miikka Vikkula, Michael T. Dellinger

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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6

A Gene for Inherited Cutaneous Venous Anomalies (“Glomangiomas”) Localizes to Chromosome 1p21-22 mā Laurence M. Boon, Pascal Brouillard, Alexandre Irrthum, Leena Karttunen, Matthew L. Warman, Ross Rudolph, John B. Mulliken, Bjørn R. Olsen, Miikka Vikkula

I whakaputaina 1999

Whiwhi kuputuhi katoa
Artigo

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7

Mutations in a Novel Factor, Glomulin, Are Responsible for Glomuvenous Malformations (“Glomangiomas”) mā Pascal Brouillard, Laurence M. Boon, John B. Mulliken, O Enjolras, Michella Ghassibe‐Sabbagh, Matthew L. Warman, Oon Tian Tan, Bjørn R. Olsen, Miikka Vikkula

I whakaputaina 2002

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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8

Association of <i>PDGFRB</i> Mutations With Pediatric Myofibroma and Myofibromatosis mā Guillaume Dachy, Ronald R. de Krijger, Sylvie Fraïtag, Ivan Théate, Bénédicte Brichard, Suma B. Hoffman, Louis Libbrecht, Florence A. Arts, Pascal Brouillard, Miikka Vikkula, Nisha Limaye, Jean‐Baptiste Demoulin

I whakaputaina 2019

Whiwhi kuputuhi katoa
Artigo

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9

Somatic Uniparental Isodisomy Explains Multifocality of Glomuvenous Malformations mā Mustapha Amyere, Virginie Aerts, Pascal Brouillard, Brendan A.S. McIntyre, François P. Duhoux, Michel Wassef, O Enjolras, John B. Mulliken, Olivier Devuyst, Hélène Antoine‐Poirel, Laurence M. Boon, Miikka Vikkula

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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10

Blockade of VEGF-C signaling inhibits lymphatic malformations driven by oncogenic PIK3CA mutation mā Inés Martínez‐Corral, Yan Zhang, Milena Petkova, Henrik Ortsäter, Sofie Sjöberg, Sandra D. Castillo, Pascal Brouillard, Louis Libbrecht, Dieter Saur, Mariona Graupera, Kari Alitalo, Laurence M. Boon, Miikka Vikkula, Taija Mäkinen

I whakaputaina 2020

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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11

Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema mā Antonella Mendola, Matthieu J. Schlögel, Arash Ghalamkarpour, Alexandre Irrthum, Ha‐Long Nguyen, Elodie Fastré, Anette Bygum, Cees van der Vleuten, Christina Fagerberg, Eulàlia Baselga, I. Quéré, John B. Mulliken, Laurence M. Boon, Pascal Brouillard, Miikka Vikkula

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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12

Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations mā Pascal Brouillard, Matthieu J. Schlögel, Nassim Homayun Sepehr, Raphaël Helaers, Angela Queisser, Elodie Fastré, Simon Boutry, Sandra Schmitz, Philippe Clapuyt, Frank Hammer, A. Dompmartin, Annamaria Weitz-Tuoretmaa, Jussi Laranne, L. Pasquesoone, Catheline Vilain, Laurence M. Boon, Miikka Vikkula

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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13

Preliminary results of the European multicentric phase III trial regarding sirolimus in slow-flow vascular malformations mā Emmanuel Seront, An Van Damme, Catherine Legrand, Annouk Bisdorff-Bresson, Philippe Orcel, Thomas Funck‐Brentano, Marie‐Antoinette Sevestre, A. Dompmartin, I. Quéré, Pascal Brouillard, Nicole Revençu, Martina De Bortoli, Frank Hammer, Philippe Clapuyt, Dana Dumitriu, Miikka Vikkula, Laurence M. Boon

I whakaputaina 2023

Whiwhi kuputuhi katoa
Artigo

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14

Genotypes and Phenotypes of 162 Families with a <b><i>Glomulin</i></b> Mutation mā Pascal Brouillard, Laurence M. Boon, Nicole Revençu, J. Berg, A. Dompmartin, Josée Dubois, Maria C. Garzón, Simon Holden, Loshan Kangesu, Christine Labrèze, Sally Ann Lynch, C McKeown, Raimundas Meškauskas, I. Quéré, Samira Syed, P. Vabres, Michel Wassef, John B. Mulliken, Miikka Vikkula

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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15

An endothelial SOX18-mevalonate pathway axis enables repurposing of statins for infantile hemangioma mā Annegret Holm, Matthew S. Graus, Jill Wylie‐Sears, J. Tan, Maya Alvarez-Harmon, Luke Borgelt, Sana Nasim, Long Hoa Chung, Ashish Jain, Mingwei Sun, Liang Sun, Pascal Brouillard, Ramrada Lekwuttikarn, Yanfei Qi, Joyce Teng, Miikka Vikkula, Harry P. Kozakewich, John B. Mulliken, Mathias François, Joyce Bischoff

I whakaputaina 2025

Whiwhi kuputuhi katoa
Artigo

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