S. Cuvertino

发表

SOX7 promotes the maintenance and proliferation of B cell precursor acute lymphoblastic cells

V. Kouskoff, V. Saha, G. Lacaud, 2016, Oncotarget.

Germline intergenic duplications at Xq26.1 underlie Bazex–Dupré–Christol basal cell carcinoma susceptibility syndrome *

S. Eyre, Z. Miedzybrodzka, J. Lear, 2022, The British journal of dermatology.

Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidine

Carol J. Saunders, C. Saunders, W. Newman, 2021, Nature communications.

SOX7-enforced expression promotes the expansion of adult blood progenitors and blocks B-cell development

V. Kouskoff, G. Lacaud, S. Cuvertino, 2016, Open Biology.

ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder

K. Devriendt, J. Clayton-Smith, S. Bhaskar, 2017, American journal of human genetics.

In Vivo Repopulating Activity Emerges at the Onset of Hematopoietic Specification during Embryonic Stem Cell Differentiation

V. Kouskoff, S. Pearson, G. Lacaud, 2015, Stem cell reports.

Haploinsufficiency of ATP6V0C possibly underlies 16p13.3 deletions that cause microcephaly, seizures, and neurodevelopmental disorder

S. Garg, S. Banka, G. Burghel, 2020, American journal of medical genetics. Part A.

Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidine

C. Saunders, A. Fry, V. Faundes, 2021, Nature Communications.

Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia

S. Lovell, S. Ferdinandusse, H. van Lenthe, 2019, Brain : a journal of neurology.

The MET oncogene transforms human primary bone‐derived cells into osteosarcomas by targeting committed osteo‐progenitors

K. Scotlandi, R. Calogero, F. Fagioli, 2012, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Germline intergenic duplications at Xq26.1 underlie Bazex-Dupre-Christol syndrome, an inherited basal cell carcinoma susceptibility condition

S. Eyre, W. Newman, Z. Miedzybrodzka, 2022, medRxiv.

Emerging concepts for the in vitro derivation of murine haematopoietic stem and progenitor cells

V. Kouskoff, Kiran Batta, Magdalena Florkowska, 2016, FEBS letters.

A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome

Colin A. Johnson, Vagheesh M. Narasimhan, A. Barton, 2020, Genetics in Medicine.

KMT2D haploinsufficiency in Kabuki syndrome disrupts neuronal function through transcriptional and chromatin rewiring independent of H3K4-monomethylation

P. Germain, T. Kleefstra, G. Merla, 2021, bioRxiv.

Effect of a retinoic acid analogue on BMP-driven pluripotent stem cell chondrogenesis

M. Domingos, Steven Woods, S. Kimber, 2023, bioRxiv.