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Mutations in the PRRT2 and the TMEM151A gene. A Schematic drawing of ...
Locations of the seven mutations in the PRRT2 sequence. (a) DNA ...
PCR gel results of four PRRT2 gene exons. M, DNA marker; lanes 1-5 ...
Diagram of the PRRT2 and missense variants. PRRT2 contains four exons ...
PRRT2 missense mutations cluster near C‐terminus and frequently lead to ...
Prrt2 expression throughout the developing mouse brain and spinal cord ...
Mutations of the PRRT2 gene. (A) Sanger sequencing of codons 214-220 of ...
Expression pattern of PRRT2 mRNA. A. Schematic representation of the ...
PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental ...
Genetic and phenotypic analyses of PRRT2 positive and negative ...
PRRT2 is a synaptic and epilepsy network hub a Human brain ...
Quantitative PCR validation of whole PRRT2 gene deletion. Y‐axes ...
PRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and ...
The intramembrane COOH-terminal domain of PRRT2 regulates voltage ...
PRRT2 Is a Key Component of the Ca2+-Dependent Neurotransmitter Release ...
PRRT2 is enriched in the growth cones of in vitro developing neurons ...
PRRT2 Mutant Leads to Dysfunction of Glutamate Signaling
PRRT2 variants identified in individuals from worldwide populations. A ...
Functional study and pathogenicity classification of PRRT2 missense ...
Functional Characterization and Pathogenicity Classification of PRRT2 ...
PRRT2 Mutations in Paroxysmal Kinesigenic Dyskinesia with Infantile ...
PRRT2 regulates SNARE complex formation and vesicle docking. (A ...
Prrt2 knockout alters Purkinje cell short-term facilitation and ...
| PRRT2 gene structure and locations of PRRT2 mutations in the PRRT2 ...
Prrt2 colocalized with presynaptic and postsynaptic markers of ...
PRRT2 Gene - GeneCards | PRRT2 Protein | PRRT2 Antibody
Interaction of Prrt2 with the GluA1 subunit in vivo and in vitro. (A ...
Presynaptic PRRT2 Deficiency Causes Cerebellar Dysfunction and ...
PRRT2 modulates presynaptic Ca2+ influx by interacting with P/Q-type ...
A Novel Truncation Mutation of the PRRT2 Gene Resulting in a 16‐Amino ...
Molecular analysis of PRRT2 gene in a case of paroxysmal kinesigenic ...
Five PRRT2 identified mutations in PKD/IC patients. (a)... | Download ...
PRRT2 coding variants identified in this study. Schematic diagram of ...
PRRT2 gene variant in a child with dysmorphic features, congenital ...
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype ...
PRRT2 Blocks Ca 2+-Regulated Exocytosis under Both Reconstituted and ...
Frontiers | PRRT2 gene mutations associated with infantile convulsions ...
PRRT2 Regulates Synaptic Fusion by Directly Modulating SNARE Complex ...
Schematic diagram showing effects of PRRT2 mutation on neuronal ...
PRRT2 gene structure and locations of PRRT2 mutations in the PRRT2 gene ...
The predicted protein consequence of mutations in the PRRT2 gene. Red ...
Expression and localization of PRRT2 in hippocampal neurons (A ...
PRRT2 KO growth cones had an increased local actin and pTyr397FAK ...
Intronic PRRT2 mutation generates novel splice acceptor site and causes ...
(PDF) Molecular analysis of PRRT2 gene in a case of paroxysmal ...
PRRT2 is mutated in familial and non-familial benign infantile seizures ...
PRRT2 and the β4-subunit have opposite effects on the expression of the ...
Cerebellar cortex vesical localization in Prrt2 +/+ and Prrt2 À/À mice ...
Functional characterization of a novel PRRT2 variant found in a ...
PRRT2 and β4-subunit independently modulate the NaV1.2 persistent and ...
A novel PRRT2 pathogenic variant in a family with paroxysmal ...
Figure 1 from Novel mutation of the PRRT2 gene in two cases of ...
Downregulation of PRRT2 in glioblastoma. (A) Real-time PCR was used to ...
(PDF) The Spectrum of PRRT2 mutations experience from a Pediatric ...
Mutation effect in PRRT2 and PNKD frameshift mutations. (A) Schematic ...
PRRT2 and the NaV β4-subunit have opposite effects on membrane ...
Novel and de novo point and large microdeletion mutation in PRRT2 ...
Role of PRRT2 in common paroxysmal neurological disorders: a gene with ...
(a) Schematic diagram of the mutations identified in the PRRT2 gene ...
Table 1 from Molecular analysis of PRRT2 gene in a case of paroxysmal ...
PRRT2 and the NaV β4-subunit do not interact or compete for binding to ...
PRRT2 frameshift mutation reduces its mRNA stability resulting loss of ...
Mutations in PRRT2 result in paroxysmal dyskinesias with marked ...
PRRT2 - Wikipedia
PRRT2 deficiency reduces the Ca 2+ -induced enhancement of eEPSC ...
Schematic diagram of proline-rich transmembrane protein 2 (PRRT2 ...
PRRT2: from Paroxysmal Disorders to Regulation of Synaptic Function ...
Expression, function and interaction network of PRRT2. ( A ) Expression ...
Protein levels of wild‐type and mutant PRRT2. A, Western blot analysis ...
Frontiers | Clinical characteristics and genetics of ten Chinese ...
Compound heterozygosity with PRRT2: Pushing the phenotypic envelope in ...
【进展】Prrt2基因缺失如何导致PKD运动障碍？
Frontiers | The Spectrum of PRRT2-Associated Disorders: Update on ...
Cell Research ︱Prrt2 基因缺失如何导致 PKD 运动障碍？ - 丁香园
A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2 ...
Exploring epileptic phenotypes in PRRT2-related disorders: A report of ...
Proline-rich transmembrane protein 2 (PRRT2) regulates the actin ...
The Tissue Expression Patterns of Mouse Prrt2; Related to Figure 5 ...
PRRT2-KO cortical networks display heightened excitability under basal ...
A Novel Topology of Proline-rich Transmembrane Protein 2 (PRRT2): HINTS ...
