受强制性开放获取政策约束的文章 - Pierre Vabres了解详情
无法在其他位置公开访问的文章：9 篇
查看
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma
C Bertolotto, F Lesueur, S Giuliano, T Strub, M De Lichy, K Bille, P Dessen, ...
Nature 480 (7375), 94-98, 2011
强制性开放获取政策： National Institute of Health and Medical Research, France, Government of Spain
查看
First-line rituximab combined with short-term prednisone versus prednisone alone for the treatment of pemphigus (Ritux 3): a prospective, multicentre, parallel-group, open …
P Joly, M Maho-Vaillant, C Prost-Squarcioni, V Hebert, E Houivet, S Calbo, ...
The Lancet 389 (10083), 2031-2040, 2017
强制性开放获取政策： National Institute of Health and Medical Research, France
查看
Mosaic‐activating FGFR2 mutation in two fetuses with papillomatous pedunculated sebaceous naevus
P Kuentz, S Fraitag, M Gonzales, F Dhombres, J St‐Onge, Y Duffourd, ...
British Journal of Dermatology 176 (1), 204-208, 2017
强制性开放获取政策： US National Institutes of Health
查看
Clinical and neuroimaging findings in 33 patients with MCAP syndrome: a survey to evaluate relevant endpoints for future clinical trials
A Garde, L Guibaud, A Goldenberg, F Petit, R Dard, J Roume, ...
Clinical Genetics 99 (5), 650-661, 2021
强制性开放获取政策： Agence Nationale de la Recherche
查看
Congenital plaque‐type glomuvenous malformations associated with fetal pleural effusion and ascites
E Goujon, KM Cordoro, M Barat, T Rousseau, P Brouillard, M Vikkula, ...
Pediatric dermatology 28 (5), 528-531, 2011
强制性开放获取政策： US National Institutes of Health
查看
Mosaicism due to postzygotic mutations in women with focal dermal hypoplasia
L Heinz, E Bourrat, P Vabres, J Thevenon, A Hotz, S Hörer, J Küsel, ...
British Journal of Dermatology 180 (3), 657-661, 2019
强制性开放获取政策： German Research Foundation
查看
Low risk of embryonic and other cancers in PIK3CA‐related overgrowth spectrum: Impact on screening recommendations
L Faivre, JC Crépin, M Réda, S Nambot, V Carmignac, C Abadie, ...
Clinical Genetics 104 (5), 554-563, 2023
强制性开放获取政策： Agence Nationale de la Recherche
查看
Clinical phenotype of the PIK3R1-related vascular overgrowth syndrome
P Kuentz, C Engel, M Laeng, M Chevarin, Y Duffourd, J Martel, J Piard, ...
British Journal of Dermatology, ljae167, 2024
强制性开放获取政策： Agence Nationale de la Recherche
查看
Expanding the clinical spectrum of mosaic BRAF skin phenotypes
A Sorlin, V Carmignac, J Amiel, O Boccara, S Fraitag, A Maruani, ...
Journal of the European Academy of Dermatology and Venereology 35 (10), e690 …, 2021
强制性开放获取政策： National Institute of Health and Medical Research, France, Agence Nationale …
可在其他位置公开访问的文章：36 篇
查看
Autoantibodies neutralizing type I IFNs are present in~ 4% of uninfected individuals over 70 years old and account for~ 20% of COVID-19 deaths
P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, J Manry, ...
Science immunology 6 (62), eabl4340, 2021
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, National …
查看
X-linked recessive TLR7 deficiency in~ 1% of men under 60 years old with life-threatening COVID-19
T Asano, B Boisson, F Onodi, D Matuozzo, M Moncada-Velez, ...
Science immunology 6 (62), eabl4348, 2021
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, National …
查看
Germline loss-of-function mutations in EPHB4 cause a second form of capillary malformation-arteriovenous malformation (CM-AVM2) deregulating RAS-MAPK signaling
M Amyere, N Revencu, R Helaers, E Pairet, E Baselga, M Cordisco, ...
Circulation 136 (11), 1037-1048, 2017
强制性开放获取政策： US National Institutes of Health, National Fund for Scientific Research, Belgium
查看
Mosaic activating mutations in GNA11 and GNAQ are associated with phakomatosis pigmentovascularis and extensive dermal melanocytosis
AC Thomas, Z Zeng, JB Rivière, R O’shaughnessy, L Al-Olabi, JS Onge, ...
Journal of Investigative Dermatology 136 (4), 770-778, 2016
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
查看
Safety and efficacy of low-dose sirolimus in the PIK3CA-related overgrowth spectrum
VER Parker, KM Keppler-Noreuil, L Faivre, M Luu, NL Oden, L De Silva, ...
Genetics in Medicine 21 (5), 1189-1198, 2019
强制性开放获取政策： US National Institutes of Health, National Institute for Health Research, UK …
查看
The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies
J Manry, P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, ...
Proceedings of the National Academy of Sciences 119 (21), 2022
强制性开放获取政策： Fundação de Amparo à Pesquisa do Estado de São Paulo, US National Institutes …
查看
In-frame mutations in exon 1 of SKI cause dominant Shprintzen-Goldberg syndrome
V Carmignac, J Thevenon, L Adès, B Callewaert, S Julia, ...
The American Journal of Human Genetics 91 (5), 950-957, 2012
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders)
查看
Lysosomal signaling licenses embryonic stem cell differentiation via inactivation of Tfe3
F Villegas, D Lehalle, D Mayer, M Rittirsch, MB Stadler, M Zinner, ...
Cell stem cell 24 (2), 257-270. e8, 2019
强制性开放获取政策： European Commission
查看
Dacarbazine-mediated upregulation of NKG2D ligands on tumor cells activates NK and CD8 T cells and restrains melanoma growth
A Hervieu, C Rébé, F Végran, F Chalmin, M Bruchard, P Vabres, L Apetoh, ...
Journal of Investigative Dermatology 133 (2), 499-508, 2013
强制性开放获取政策： National Institute of Health and Medical Research, France
查看
Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas
E Bal, HS Park, Z Belaid-Choucair, H Kayserili, M Naville, M Madrange, ...
Nature medicine 23 (10), 1226-1233, 2017
强制性开放获取政策： Swiss National Science Foundation
查看
Genotypes and phenotypes of 162 families with a glomulin mutation
P Brouillard, LM Boon, N Revencu, J Berg, A Dompmartin, J Dubois, ...
Molecular syndromology 4 (4), 157-164, 2013
强制性开放获取政策： US National Institutes of Health
出版信息和资助信息由计算机程序自动确定