MMG PUBLICATIONS

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Results: 3220  publications found.

Cavodeassi, F.  et al. 2019

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. These range from massive malformations of the brain and ocular primordia,...
- issue: 8-9, SI - volume: 138 - pages: 917-936.

Uboldi, C.  et al. 2019

In Vitro Analysis of the Effects of ITER-Like Tungsten Nanoparticles: Cytotoxicity and Epigenotoxicity in BEAS-2B Cells

Tungsten was chosen as a wall component to interact with the plasma generated by the International Thermonuclear Experimental fusion Reactor (ITER). Nevertheless, during plasma operation tritiated...
Nanomaterials (Basel) - issue: 9 - volume: 9 - pages: .

Zaravinos, A.  et al. 2019

Cytolytic activity correlates with the mutational burden and deregulated expression of immune checkpoints in colorectal cancer

- issue: 1 - volume: 38 - pages: .

Zaravinos, A.  et al. 2019

Cytolytic activity correlates with the mutational burden and deregulated expression of immune checkpoints in colorectal cancer

BackgroundMicrosatellite unstable colorectal cancers (MSI+ CRCs) expressing PD-L1, respond to anti-PD-1 or anti-PD-L1 checkpoint blockade, whereas microsatellite-stable tumors do not respond the same....
- issue: 1 - volume: 38 - pages: .

Chabbert, D.  et al. 2019

Postnatal Tshz3 Deletion Drives Altered Corticostriatal Function and Autism Spectrum Disorder-like Behavior

- issue: 4 - volume: 86 - pages: 274-285.

Chabbert, D.  et al. 2019

Postnatal Tshz3 Deletion Drives Altered Corticostriatal Function and Autism Spectrum Disorder-like Behavior

BACKGROUND: Heterozygous deletion of the TSHZ3 gene, encoding for the teashirt zinc-finger homeobox family member 3 (TSHZ3) transcription factor that is highly expressed in cortical projection neurons...
- issue: 4 - volume: 86 - pages: 274-285.

Francastel, C.  et al. 2019

DNA methylation in satellite repeats disorders

Despite the tremendous progress made in recent years in assembling the human genome, tandemly repeated DNA elements remain poorly characterized. These sequences account for the vast majority of...
Essays Biochem. - issue: - volume: - pages: .

Neumann, HPH.  et al. 2019

Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy.

IMPORTANCE: Large studies investigating long-term outcomes of patients with bilateral pheochromocytomas treated with either total or cortical-sparing adrenalectomies are needed to inform clinical...
JAMA Netw Open - issue: 8 - volume: 2 - pages: e198898.

Mondielli, G.  et al. 2019

TARGETING PI3K-AKT-MTOR AND MAP-KINASE PATHWAYS IN AGGRESSIVE MENINGIOMAS: IN VITRO STUDY

- issue: 3 - volume: 21 - pages: 17.

Mignot, C.  et al. 2019

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients (vol 21, pg 837, 2019)

- issue: 8 - volume: 21 - pages: 1897-1898.

Studen, KB.  et al. 2019

Genetic analysis of adult Slovenian patients with combined pituitary hormone deficiency

- issue: 2 - volume: 65 - pages: 379-385.

Mika, D.  et al. 2019

Synergic PDE3 and PDE4 control intracellular cAMP and cardiac excitation-contraction coupling in a porcine model

- issue: - volume: 133 - pages: 57-66.

Grapperon, A.  et al. 2019

Quantitative Brain Sodium MRI Depicts Corticospinal Impairment in Amyotrophic Lateral Sclerosis

- issue: 2 - volume: 292 - pages: 422-428.

Chatonnet, A.  et al. 2019

An evolutionary perspective on the first disulfide bond in members of the cholinesterase-carboxylesterase (COesterase) family: Possible outcomes for cholinesterase expression in prokaryotes

- issue: - volume: 308 - pages: 179-184.

Theraulaz, G.  et al. 2019

In memoriam Jacques Gervet (1934-2018)

- issue: 3 - volume: 66 - pages: 501-502.

Fabre, A.  et al. 2019

Clinical Aspects of STAT3 Gain-of-Function Germline Mutations: A Systematic Review

- issue: 6 - volume: 7 - pages: 1958+.

Bajuk Studen, K.  et al. 2019

Genetic analysis of adult Slovenian patients with combined pituitary hormone deficiency.

PURPOSE: Among genetic causes of combined pituitary hormone deficiency (CPHD), mutations of genes coding for transcription factors involved in pituitary development have been implicated. Congenital...
Endocrine - issue: 2 - volume: 65 - pages: 379-385.

Mondielli, G.  et al. 2019

TARGETING PI3K-AKT-MTOR AND MAPKINASE PATHWAYS IN AGGRESSIVE MENINGIOMAS: IN VITRO STUDY

- issue: 3 - volume: 21 - pages: 17.

Mignot, C.  et al. 2019

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients (vol 21, pg 837, 2019)

- issue: 8 - volume: 21 - pages: 1897-1898.

Studen, KB.  et al. 2019

Genetic analysis of adult Slovenian patients with combined pituitary hormone deficiency

PurposeAmong genetic causes of combined pituitary hormone deficiency (CPHD), mutations of genes coding for transcription factors involved in pituitary development have been implicated. Congenital CPHD...
- issue: 2 - volume: 65 - pages: 379-385.