Các bài viết có thể truy cập công khai - Gérard TachdjianTìm hiểu thêm
Không có ở bất kỳ nơi nào: 1
KDM1A genotyping and expression in 146 sporadic somatotroph pituitary adenomas
F Chasseloup, D Regazzo, L Tosca, A Proust, E Kuhn, M Hage, C Jublanc, ...
European Journal of Endocrinology 190 (2), 173-181, 2024
Các cơ quan ủy nhiệm: National Institute of Health and Medical Research, France, Agence Nationale …
Có tại một số nơi: 17
Towards a clinical use of human embryonic stem cell-derived cardiac progenitors: a translational experience
P Menasche, V Vanneaux, JR Fabreguettes, A Bel, L Tosca, S Garcia, ...
European heart journal 36 (12), 743-750, 2015
Các cơ quan ủy nhiệm: National Institute of Health and Medical Research, France
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development
J Young, C Metay, J Bouligand, B Tou, B Francou, L Maione, L Tosca, ...
Human Reproduction 27 (5), 1460-1465, 2012
Các cơ quan ủy nhiệm: National Institute of Health and Medical Research, France
Level of RUNX1 activity is critical for leukemic predisposition but not for thrombocytopenia
I Antony-Debré, VT Manchev, N Balayn, D Bluteau, C Tomowiak, ...
Blood, The Journal of the American Society of Hematology 125 (6), 930-940, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health
Loss of KDM1A in GIP-dependent primary bilateral macronodular adrenal hyperplasia with Cushing's syndrome: a multicentre, retrospective, cohort study
F Chasseloup, I Bourdeau, A Tabarin, D Regazzo, C Dumontet, ...
The lancet Diabetes & endocrinology 9 (12), 813-824, 2021
Các cơ quan ủy nhiệm: Fonds de recherche du Québec - Santé, National Institute of Health and …
Genomic alterations and complex subclonal architecture in sporadic GH-secreting pituitary adenomas
M Hage, S Viengchareun, E Brunet, C Villa, D Pineau, J Bouligand, ...
The Journal of Clinical Endocrinology & Metabolism 103 (5), 1929-1939, 2018
Các cơ quan ủy nhiệm: National Institute of Health and Medical Research, France
Adrenal GIPR expression and chromosome 19q13 microduplications in GIP-dependent Cushing’s syndrome
AL Lecoq, CA Stratakis, S Viengchareun, R Chaligné, L Tosca, ...
JCI insight 2 (18), e92184, 2017
Các cơ quan ủy nhiệm: US National Institutes of Health, National Institute of Health and Medical …
Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player
T Celse, C Cazin, F Mietton, G Martinez, D Martinez, N Thierry-Mieg, ...
Human Genetics 140, 43-57, 2021
Các cơ quan ủy nhiệm: Agence Nationale de la Recherche
Genomic instability of human embryonic stem cell lines using different passaging culture methods
L Tosca, O Feraud, A Magniez, C Bas, F Griscelli, A Bennaceur-Griscelli, ...
Molecular cytogenetics 8, 1-11, 2015
Các cơ quan ủy nhiệm: National Institute of Health and Medical Research, France
Disrupted filamin A/αIIbβ3 interaction induces macrothrombocytopenia by increasing RhoA activity
A Donada, N Balayn, D Sliwa, L Lordier, V Ceglia, F Baschieri, C Goizet, ...
Blood, The Journal of the American Society of Hematology 133 (16), 1778-1788, 2019
Các cơ quan ủy nhiệm: European Commission, Agence Nationale de la Recherche
Stepwise GATA1 and SMC3 mutations alter megakaryocyte differentiation in a Down syndrome leukemia model
B Arkoun, E Robert, F Boudia, S Mazzi, V Dufour, A Siret, Y Mammasse, ...
The Journal of clinical investigation 132 (14), 2023
Các cơ quan ủy nhiệm: National Institute of Health and Medical Research, France, Swiss Cancer League
Hypermethylator phenotype and ectopic GIP receptor in GNAS mutation-negative somatotropinomas
M Hage, R Chaligne, S Viengchareun, C Villa, S Salenave, J Bouligand, ...
The Journal of Clinical Endocrinology & Metabolism 104 (5), 1777-1787, 2019
Các cơ quan ủy nhiệm: National Institute of Health and Medical Research, France
Integration-deficient lentivectors: an effective strategy to purify and differentiate human embryonic stem cell-derived hepatic progenitors
G Yang, K Si-Tayeb, S Corbineau, R Vernet, R Gayon, N Dianat, ...
BMC biology 11, 1-16, 2013
Các cơ quan ủy nhiệm: UK Medical Research Council, Wellcome Trust
Transplantation of Macaca cynomolgus iPS-derived hematopoietic cells in NSG immunodeficient mice
S Abed, A Tubsuwan, P Chaichompoo, IH Park, A Pailleret, A Benyoucef, ...
Haematologica 100 (10), e428, 2015
Các cơ quan ủy nhiệm: National Institute of Health and Medical Research, France
Critical contribution of mitochondria in the development of cardiomyopathy linked to desmin mutation
Y Hovhannisyan, Z Li, D Callon, R Suspène, V Batoumeni, A Canette, ...
Stem cell research & therapy 15 (1), 10, 2024
Các cơ quan ủy nhiệm: National Institute of Health and Medical Research, France, Fondazione …
Improved functionality of hepatic spheroids cultured in acoustic levitation compared to existing 2D and 3D models
L Rabiet, N Jeger-Madiot, DR García, L Tosca, G Tachdjian, S Kellouche, ...
Scientific Reports 14 (1), 21528, 2024
Các cơ quan ủy nhiệm: Agence Nationale de la Recherche
Generation of human induced pluripotent stem cell lines from five patients with Myofibrillar myopathy carrying different heterozygous mutations in the DES gene
P Joanne, Y Hovhannisyan, A Simon, G Revet, R Diot, G Friob, D Calin, ...
Stem Cell Research 76, 103338, 2024
Các cơ quan ủy nhiệm: National Institute of Health and Medical Research, France, Fondazione …
An early onset benign myopathy with glycogen storage caused by a de novo 1.4 Mb-deletion of chromosome 14
G Severa, A Pennisi, C Barnerias, C Fiorillo, M Scala, V Taglietti, ...
Neuromuscular Disorders 33 (10), 817-821, 2023
Các cơ quan ủy nhiệm: Agence Nationale de la Recherche
Chương trình máy tính sẽ tự động xác định thông tin xuất bản và thông tin về nhà tài trợ