MMG PUBLICATIONS

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Results: 3193  publications found.

Richart, A.  et al. 2014

MicroRNA-21 Coordinates Human Multipotent Cardiovascular Progenitors Therapeutic Potential

Published clinical trials in patients with ischemic diseases show limited benefit of adult stem cell-based therapy, likely due to their restricted plasticity and commitment toward vascular cell...
Stem Cells - issue: 11 - volume: 32 - pages: 2908-2922.

Lacoste, C.  et al. 2014

Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome

WOS:000344004800017
Clin. Genet. - issue: 5 - volume: 86 - pages: 502-503.

Gorincour, G.  et al. 2014

Fetal skeletal computed tomography: When? How? Why?

Purpose: To study the additional role of fetal skeletal computed tomography in suspected prenatal bone abnormalities. Materials and methods: Two centers included in a retrospective study all fetuses...
Diagn. Interv. Imaging - issue: 11 - volume: 95 - pages: 1045-1053.

Bonello-Palot, N.  et al. 2014

Prelamin A accumulation in endothelial cells induces premature senescence and functional impairment

BACKGROUND: Defects in lamin A maturation result in premature aging syndromes and severe atherosclerosis as observed in the Hutchinson-Gilford Progeria Syndrome. In age-related atherosclerosis,...
Atherosclerosis - issue: 1 - volume: 237 - pages: 45-52.

Mohan, RA.  et al. 2014

A Mutation in the Kozak Sequence of GATA4 Hampers Translation in a Family With Atrial Septal Defects

Atrial septal defect (ASD) is the most common congenital heart defect clinically characterized by an opening in the atrial septum. Mutations in GATA4, TBX5, and NKX2-5 underlie this phenotype. Here,...
Am. J. Med. Genet. A - issue: 11 - volume: 164 - pages: 2732-2738.

Bonello-Palot, N.  et al. 2014

Prelamin A accumulation in endothelial cells induces premature senescence and functional impairment

BACKGROUND: Defects in lamin A maturation result in premature aging syndromes and severe atherosclerosis as observed in the Hutchinson-Gilford Progeria Syndrome. In age-related atherosclerosis,...
Atherosclerosis - issue: 1 - volume: 237 - pages: 45-52.

Mohan, RA.  et al. 2014

A mutation in the Kozak sequence of GATA4 hampers translation in a family with atrial septal defects.

Atrial septal defect (ASD) is the most common congenital heart defect clinically characterized by an opening in the atrial septum. Mutations in GATA4, TBX5, and
Am J Med Genet A - issue: 11 - volume: 164A - pages: 2732-2738.

Griffin, LB.  et al. 2014

Impaired function is a common feature of neuropathy-associated glycyl-tRNA synthetase mutations

Charcot-Marie-Tooth disease type 2D (CMT2D) is an autosomal-dominant axonal peripheral neuropathy characterized by impaired motor and sensory function in the distal extremities. Mutations in the...
Hum. Mutat. - issue: 11 - volume: 35 - pages: 1363-1371.

Gadelha, MR.  et al. 2014

Pasireotide versus continued treatment with octreotide or lanreotide in patients with inadequately controlled acromegaly (PAOLA): a randomised, phase 3 trial

BACKGROUND: Many patients with acromegaly do not achieve biochemical control despite receiving high doses of the first-generation somatostatin analogues octreotide or lanreotide. In the PAOLA trial,...
Lancet Diabetes Endocrinol - issue: 11 - volume: 2 - pages: 875-884.

Richart, A.  et al. 2014

MicroRNA-21 coordinates human multipotent cardiovascular progenitors therapeutic potential

Published clinical trials in patients with ischemic diseases show limited benefit of adult stem cell-based therapy, likely due to their restricted plasticity and commitment toward vascular cell...
Stem Cells - issue: 11 - volume: 32 - pages: 2908-2922.

Falcone, S.  et al. 2014

N-WASP is required for Amphiphysin-2/BIN1-dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy

Mutations in amphiphysin-2/BIN1, dynamin 2, and myotubularin are associated with centronuclear myopathy (CNM), a muscle disorder characterized by myofibers with atypical central nuclear positioning...
EMBO Mol Med - issue: 11 - volume: 6 - pages: 1455-1475.

Lacoste, C.  et al. 2014

Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome

Clin. Genet. - issue: 5 - volume: 86 - pages: 502-503.

Lacoste, C.  et al. 2014

Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome

Clin. Genet. - issue: 5 - volume: 86 - pages: 502-503.

Bonello-Palot, N.  et al. 2014

Prelamin A accumulation in endothelial cells induces premature senescence and functional impairment

Background: Defects in lamin A maturation result in premature aging syndromes and severe atherosclerosis as observed in the Hutchinson-Gilford Progeria Syndrome. In age-related atherosclerosis,...
Atherosclerosis - issue: 1 - volume: 237 - pages: 45-52.

Sussman, MA.  et al. 2014

Response to Letter Regarding Article, "Embryonic Stem Cell-Derived Cardiac Myocytes Are Not Ready for Human Trials"

WOS:000343762700002
Circ.Res. - issue: 10 - volume: 115 - pages: E30-E31.

Sussman, MA.  et al. 2014

Response to letter regarding article, "Embryonic stem cell-derived cardiac myocytes are not ready for human trials"

Circ. Res. - issue: 10 - volume: 115 - pages: e30-31.

Sussman, MA.  et al. 2014

Response to letter regarding article, "Embryonic stem cell-derived cardiac myocytes are not ready for human trials"

Circ. Res. - issue: 10 - volume: 115 - pages: e30-31.

Sussman, MA.  et al. 2014

Response to letter regarding article, "Embryonic stem cell-derived cardiac myocytes are not ready for human trials"

Circ Res - issue: 10 - volume: 115 - pages: e30-31.

Rana, MS.  et al. 2014

Tbx1 Coordinates Addition of Posterior Second Heart Field Progenitor Cells to the Arterial and Venous Poles of the Heart

Rationale: Cardiac progenitor cells from the second heart field (SHF) contribute to rapid growth of the embryonic heart, giving rise to right ventricular and outflow tract (OFT) myocardium at the...
Circ.Res. - issue: 9 - volume: 115 - pages: 790-U118.

Rana, MS.  et al. 2014

Tbx1 coordinates addition of posterior second heart field progenitor cells to the arterial and venous poles of the heart

RATIONALE: Cardiac progenitor cells from the second heart field (SHF) contribute to rapid growth of the embryonic heart, giving rise to right ventricular and outflow tract (OFT) myocardium at the...
Circ Res - issue: 9 - volume: 115 - pages: 790-799.