Natacha Roblot
Overview
Explore the profile of Natacha Roblot including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
589
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Recent Articles
1.
Vali A, Dalle H, Loubaresse A, Gilleron J, Havis E, Garcia M, et al.
Diabetes
. 2023 Nov;
73(2):211-224.
PMID: 37963392
Article Highlights:
2.
Komatsu J, Cico A, Poncin R, Le Bohec M, Morf J, Lipin S, et al.
Sci Rep
. 2023 Mar;
13(1):4866.
PMID: 36964177
Progress in sample preparation for scRNA-seq is reported based on RevGel-seq, a reversible-hydrogel technology optimized for samples of fresh cells. Complexes of one cell paired with one barcoded bead are...
3.
Bourgneuf C, Bailbe D, Lamaziere A, Dupont C, Moldes M, Farabos D, et al.
Nat Commun
. 2021 Feb;
12(1):1064.
PMID: 33594056
Polycystic ovary syndrome (PCOS) is characterized by an oligo-anovulation, hyperandrogenism and polycystic ovarian morphology combined with major metabolic disturbances. However, despite the high prevalence and the human and economic consequences...
4.
Auclair M, Roblot N, Capel E, Feve B, Antoine B
Am J Physiol Endocrinol Metab
. 2020 Nov;
320(2):E219-E233.
PMID: 33252251
Beiging is an attractive therapeutic strategy to fight against obesity and its side metabolic complications. The loss of function of the nuclear transcription factor RORα has been related to a...
5.
Fassier C, Tarrade A, Peris L, Courageot S, Mailly P, Dalard C, et al.
Dis Model Mech
. 2012 Jul;
6(1):72-83.
PMID: 22773755
Mutations in SPG4, encoding the microtubule-severing protein spastin, are responsible for the most frequent form of hereditary spastic paraplegia (HSP), a heterogeneous group of genetic diseases characterized by degeneration of...
6.
Vitte J, Fassier C, Tiziano F, Dalard C, Soave S, Roblot N, et al.
Am J Pathol
. 2007 Aug;
171(4):1269-80.
PMID: 17717146
Spinal muscular atrophy (SMA) is characterized by degeneration of lower motor neurons and caused by mutations of the SMN1 gene. SMN1 is duplicated in a homologous gene called SMN2, which...
7.
Tarrade A, Fassier C, Courageot S, Charvin D, Vitte J, Peris L, et al.
Hum Mol Genet
. 2006 Nov;
15(24):3544-58.
PMID: 17101632
Mutations of the spastin gene (Sp) are responsible for the most frequent autosomal dominant form of spastic paraplegia, a disease characterized by the degeneration of corticospinal tracts. We show that...
8.
Salah-Mohellibi N, Millet G, Andre-Schmutz I, Desforges B, Olaso R, Roblot N, et al.
Stem Cells
. 2006 Aug;
24(12):2723-32.
PMID: 16888281
Bone marrow (BM) transplantation was performed on a muscular mouse model of spinal muscular atrophy that had been created by mutating the survival of motor neuron gene (Smn) in myofibers...
9.
Olaso R, Joshi V, Fernandez J, Roblot N, Courageot S, Bonnefont J, et al.
Physiol Genomics
. 2005 Aug;
24(2):97-104.
PMID: 16118268
Mutations of the survival of motor neuron gene (SMN1) are responsible for spinal muscular atrophies (SMA), a frequent recessive autosomal motor neuron disease. SMN is involved in various processes including...
10.
Billat V, Mouisel E, Roblot N, Melki J
J Appl Physiol (1985)
. 2004 Nov;
98(4):1258-63.
PMID: 15542571
With the generation of mouse models of human cardiovascular or neuromuscular disorders, the development of noninvasive methods to evaluate the physiological responses to exercise presents an important challenge. The possibility...