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SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system developmentSmall Supernumerary Marker Chromosomes in Human InfertilityLevel of RUNX1 activity is critical for leukemic predisposition but not for thrombocytopenia.Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and SyndactylyTowards a clinical use of human embryonic stem cell-derived cardiac progenitors: a translational experience.Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent diseaseGenomic instability of human embryonic stem cell lines using different passaging culture methods.Induced pluripotent stem cell generation from a man carrying a complex chromosomal rearrangement as a genetic model for infertility studiesSmall supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions.Risk of tumorigenicity in mesenchymal stromal cell-based therapies--bridging scientific observations and regulatory viewpoints.Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23In Vitro Gamete Differentiation from Pluripotent Stem Cells as a Promising Therapy for Infertility.An atypical human induced pluripotent stem cell line with a complex, stable, and balanced genomic rearrangement including a large de novo 1q uniparental disomy.Messenger RNA- versus retrovirus-based induced pluripotent stem cell reprogramming strategies: analysis of genomic integrity.Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: a two-hit case with more severe clinical manifestations.Modeling the influence of stromal microenvironment in the selection of ENU-induced BCR-ABL1 mutants by tyrosine kinase inhibitors.Transplantation of Macaca cynomolgus iPS-derived hematopoietic cells in NSG immunodeficient mice.Different routes lead to apoptosis in unfertilized sea urchin eggs.SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplication.Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts.Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertility.Human embryonic stem cell-derived cardiac progenitors for severe heart failure treatment: first clinical case report: Figure 1Disrupted filamin A/αβ interaction induces macrothrombocytopenia by increasing RhoA activityTetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformationsConfined blood chimerism in a monochorionic dizygotic sex discordant twin pregnancy conceived after induced ovulation
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Q24307518-83486AE2-1791-434F-9D66-82D10CBD0B74Q26781835-73A35D5D-3EAA-4C88-B86F-83352B0DCF40Q33419236-87493896-BFB1-4686-B9C9-906663E12D5FQ33560972-354531FC-DCE9-4E7B-8734-B60BB5C7BFDAQ34041000-3A938570-490F-4505-8365-0E0116FA51C2Q35066451-D623EB1B-60F1-45B7-A5FD-4704A375BF39Q35686581-8EAF1BBF-0F1D-4E93-AF93-379FB8BE831DQ37550143-7CE9D635-51AA-4718-BB8A-0C41D45E5C0DQ38047092-0FDA1395-5B15-49AC-B44E-BBDC2374EFB0Q38100464-FB03CE92-94A9-4490-ABE6-D5213A873588Q38617714-70D58E70-9D44-4630-B443-E66F1880E46AQ38731826-BC5A4F63-4A77-4A8C-9978-9C59C2165347Q38913129-2B1C15E1-0DAA-4874-A3A1-14FEC676ABA5Q40095667-EA7C37CA-E617-4E3C-AEB6-F433B3442C13Q40750345-29196086-DDEB-4CE8-BD40-2FFD5B4A6580Q41575103-2D44BAE6-F532-4248-986F-BA594ACF1CE6Q43234206-FEDC2835-B25C-4ACC-9DB8-5D549D7A10B9Q44148988-035DFF19-8F41-4702-85DA-9D6FA57D93D7Q50691673-130F9BDF-5908-4ADE-A108-80330A521B33Q52663696-51E680D8-0C00-4770-94BE-EBE267D727CFQ54337258-8663C0B3-BD9F-4F3C-A135-AE3A1CDB5902Q61484561-23FAE39B-19BB-40AF-A590-149CA5236DA9Q64101652-71182D92-F4B5-43D1-AC54-844DEB185CCCQ83655176-426C6A71-F2FC-4D68-897B-25CB05C82F68Q95557309-2B591DDE-03BD-472D-9BD6-C9B00D1B7973
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description
researcher ORCID ID = 0000-0003-2766-8265
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wetenschapper
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name
Lucie Tosca
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Lucie Tosca
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Lucie Tosca
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Lucie Tosca
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type
label
Lucie Tosca
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Lucie Tosca
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Lucie Tosca
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Lucie Tosca
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Tosca L
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Lucie Tosca
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Lucie Tosca
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Lucie Tosca
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Lucie Tosca
@nl
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P31
P496
0000-0003-2766-8265