Michele Studer
Overview
Explore the profile of Michele Studer including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
67
Citations
2006
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Ovsthus M, van Swieten M, Puchades M, Tocco C, Studer M, Bjaalie J, et al.
Sci Data
. 2024 Nov;
11(1):1214.
PMID: 39532918
The cerebral cortex extends axonal projections to several subcortical brain regions, including the striatum, thalamus, superior colliculus, and pontine nuclei. Experimental tract-tracing studies have shown that these subcortical projections are...
2.
Bertacchi M, Maharaux G, Loubat A, Jung M, Studer M
Elife
. 2024 Nov;
13.
PMID: 39485283
The morphogen FGF8 establishes graded positional cues imparting regional cellular responses modulation of early target genes. The roles of FGF signaling and its effector genes remain poorly characterized in human...
3.
Bonzano S, Dallorto E, Bovetti S, Studer M, De Marchis S
Neurobiol Dis
. 2024 Jul;
199:106604.
PMID: 39002810
Mitochondria are essential regulators of cellular energy metabolism and play a crucial role in the maintenance and function of neuronal cells. Studies in the last decade have highlighted the importance...
4.
Cui K, Xia Y, Patnaik A, Salivara A, Lowenstein E, Isik E, et al.
Sci Adv
. 2024 Jun;
10(25):eadj0720.
PMID: 38896627
Mutations in the transcription factors encoded by or correlate with congenital central hypoventilation disorders. These conditions are typically characterized by pronounced hypoventilation, central apnea, and diminished chemoreflexes, particularly to abnormally...
5.
Marino V, Phromkrasae W, Bertacchi M, Cassini P, Chakrabandhu K, DellOrco D, et al.
Protein Sci
. 2024 Mar;
33(4):e4953.
PMID: 38511490
Deciphering the structural effects of gene variants is essential for understanding the pathophysiological mechanisms of genetic diseases. Using a neurodevelopmental disorder called Bosch-Boonstra-Schaaf Optic Atrophy Syndrome (BBSOAS) as a genetic...
6.
Deloulme J, Leclercq M, Deschaux O, Flore G, Capellano L, Tocco C, et al.
Neurobiol Dis
. 2024 Feb;
193:106455.
PMID: 38408685
White matter (WM) tract formation and axonal pathfinding are major processes in brain development allowing to establish precise connections between targeted structures. Disruptions in axon pathfinding and connectivity impairments will...
7.
Di Bonito M, Bourien J, Tizzano M, Harrus A, Puel J, Avallone B, et al.
PLoS Genet
. 2023 Sep;
19(9):e1010933.
PMID: 37738262
Autosomal recessive mutation of HOXB1 and Hoxb1 causes sensorineural hearing loss in patients and mice, respectively, characterized by the presence of higher auditory thresholds; however, the origin of the defects...
8.
Felske T, Tocco C, Peron S, Harb K, Alfano C, Galante C, et al.
PLoS Biol
. 2023 Aug;
21(8):e3002237.
PMID: 37552690
In vivo direct neuronal reprogramming relies on the implementation of an exogenous transcriptional program allowing to achieve conversion of a particular neuronal or glial cell type towards a new identity....
9.
Bonzano S, Dallorto E, Molineris I, Michelon F, Crisci I, Gambarotta G, et al.
Dis Model Mech
. 2023 Jun;
16(6).
PMID: 37260288
The nuclear receptor NR2F1 acts as a strong transcriptional regulator in embryonic and postnatal neural cells. In humans, mutations in the NR2F1 gene cause Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS), a...
10.
Studer M, Rossini L, Spreafico R, Pelliccia V, Tassi L, de Curtis M, et al.
Epilepsia
. 2022 Aug;
63(10):2716-2721.
PMID: 35932101
No abstract available.