PUBLICATIONS MMG

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Résultats : 1707  publications trouvées.

Guinde, J.  et al. 2018

Lamins in Lung Cancer: Biomarkers and Key Factors for Disease Progression through miR-9 Regulation?

Lung cancer represents the primary cause of cancer death in the world. Malignant cells identification and characterization are crucial for the diagnosis and management of patients with primary or...
- issue: 7 - volume: 7 - pages: .


Metzler-Guillemain, C.  et al. 2018

The nuclear envelope: an unknown actor of human spermiogenesis

- issue: 1 - volume: 33 - pages: 77-78.


Paci, M.  et al. 2018

The involvement of the nuclear lamina in human and rodent spermiogenesis: a systematic review

The nuclear lamina (NL) is a filamentous protein meshwork, composed essentially of lamins, situated between the inner nuclear membrane and the chromatin. The NL is a component of the nuclear envelope,...
- issue: - volume: 28 - pages: .


Cuny, T.  et al. 2018

Role of the tumor microenvironment in digestive neuroendocrine tumors

Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) represent a group of heterogeneous tumors whose incidence increased over the past few years. Around half of patients already present with...
- issue: 11 - volume: 25 - pages: R519-R544.


Jonghe, P.  et al. 2018

PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease

Background Charcot-Marie-Tooth type 2 (CMT2) neuropathy is characterised by a vast clinical and genetic heterogeneity complicating its diagnosis and therapeutic intervention. Identification of...
- issue: 8 - volume: 89 - pages: 870-878.


Ku, CR.  et al. 2018

Long-acting FC-fusion rhGH (GX-H9) shows potential for up to twice-monthly administration in GH-deficient adults

Objective: Hybrid Fc-fused rhGH (GX-H9) is a long-acting recombinant human growth hormone (GH) under clinical development for both adults and children with GH deficiency (GHD). We compared the safety,...
- issue: 3 - volume: 179 - pages: 169-179.


Matagne, V.  et al. 2018

Correcting deregulated Fxydl expression rescues deficits in neuronal arborization and potassium homeostasis in MeCP2 deficient male mice

Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the MECP2 gene. In the absence of MeCP2, expression of FXYD domain-containing transport regulator 1 (FXYD1) is deregulated...
- issue: - volume: 1697 - pages: 45-52.


Payan, S.  et al. 2018

By promoting cardiac regeneration FGF10 preserves cardiac remodeling and function after myocardial infarction

- issue: 1 - volume: 114 - pages: S78.


Neumann, HP.  et al. 2018

65 YEARS OF THE DOUBLE HELIX Genetics informs precision practice in the diagnosis and management of pheochromocytoma

Although the authors of the present review have contributed to genetic discoveries in the field of pheochromocytoma research, we can legitimately ask whether these advances have led to improvements in...
- issue: 8 - volume: 25 - pages: T201-T219.


Puceat, M.  et al. 2018

A brief overview on iPSC and embryonic stem cell technology

- issue: 12 - volume: 29 - pages: A5.


Albarel, F.  et al. 2018

Pre-surgical medical treatment, a major prognostic factor for long-term remission in acromegaly

PurposeTo determine whether pre-surgical medical treatment (PSMT) using long-acting Somatostatin analogues in acromegaly may improve long-term surgical outcome and to determine decision making...
- issue: 6 - volume: 21 - pages: 615-623.


Cavodeassi, F.  et al. 2018

The hedgehog pathway and ocular developmental anomalies

Mutations in effectors of the Hedgehog signaling pathway are responsible for a wide variety of ocular developmental anomalies (ODA). These range from massive malformations of the brain and ocular...
- issue: - volume: - pages: .


Perrin, A.  et al. 2018

Towards an harmonization of diagnosis by NGS of neuromuscular diseases

- issue: Hors-série 2 - volume: 34 - pages: 20-22.


Castinetti, F.  et al. 2018

Introduction to expert opinion on endocrine complications of new anticancer therapies

Over the last 10 years, cancer treatment has progressed, with increasing use of tyrosine kinase inhibitors, mTOR inhibitors and, most recently, immunotherapy. These molecules, however, also incur...
- issue: 5 - volume: 79 - pages: 535-538.


Pinard, A.  et al. 2018

Analysis of HOXB1 gene in a cohort of patients with sporadic ventricular septal defect

Ventricular septal defect (VSD) including outlet VSD of double outlet right ventricle (DORV) and perimembranous VSD are among the most common congenital heart diseases found at birth. HOXB1 encodes a...
- issue: 5 - volume: 45 - pages: 1507-1513.


Le Roy, A.  et al. 2018

Immunomodulatory Drugs Exert Anti-Leukemia Effects in Acute Myeloid Leukemia by Direct and Immunostimulatory Activities

Immunomodulatory drugs (IMiDs) are anticancer drugs with immunomodulatory, anti-angiogenesis, anti-proliferative, and pro-apoptotic properties. IMiDs are currently used for the treatment of multiple...
- issue: - volume: 9 - pages: 977.


Lo Cicero, A.  et al. 2018

Pathological modelling of pigmentation disorders associated with Hutchinson-Gilford Progeria Syndrome (HGPS) revealed an impaired melanogenesis pathway in iPS-derived melanocytes

Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic disorder that leads to premature aging. In this study, we used induced pluripotent stem cells to investigate the hypopigmentation...
- issue: 1 - volume: 8 - pages: .


Amouroux, M.  et al. 2018

Are men ready to use thermal male contraception? Acceptability in two French populations: New fathers and new providers

Background Since the 1970s, international research has actively pursued hormonal male contraception (HMC) and, to a lesser extent, thermal male contraception (TMC). Although the efficacy of TMC has...
- issue: 5 - volume: 13 - pages: e0195824.


Bahougne, T.  et al. 2018

Functioning Mediastinal Paraganglioma Associated with a Germline Mutation of von Hippel-Lindau Gene

We report the case of a 21-year old woman presenting with high blood pressure and raised normetanephrine levels. Indium-111-pentetreotide single photon-emission computed tomography with computed...
- issue: 6 - volume: 7 - pages: .


Balducci, E.  et al. 2018

Interphase FISH for BCR-ABL1 rearrangement on neutrophils: A decisive tool to discriminate a lymphoid blast crisis of chronic myeloid leukemia from a de novo BCR-ABL1 positive acute lymphoblastic leukemia

Discrimination between lymphoid blast crisis of chronic myeloid leukemia (CML) and de novo BCR-ABL1 positive acute lymphoblastic leukemia (ALL) represents a diagnostic challenge because this...
- issue: 1 - volume: 36 - pages: 344-348.