Syne1 Function

Syne1 MGI Mouse Gene Detail MGI1927152 spectrin repeat containing

SYNE1 Deficiency Manifesting Primarily With Motor Neuron Disease

Exemplary mechanisms of SYNE1 mutations A An exonic base exchange

CRISPR targeting of 3 end of Syne1 coding sequence disrupts Nesprin1

Generation of mice lacking nesprin 1 CH domains A Schematic of syne1

A Case Report of SYNE1 DeficiencyMimicking Mitochondrial Disease and

SYNE1 is expressed at significantly lower levels in the endometrial

The expression of SYNE1 was inhibited by lncCYP7A11 A Gene

SYNE1 mutations A Graphical overview of the mutations found in this

SYNE1 mutations identified in this study Download Table

Mutation in SYNE1 observed in the present family a Direct nucleotide

SYNE1 identified truncating mutations A Sequence traces of healthy

The expression of SYNE1 was inhibited by lncCYP7A11 A Gene

Downregulation of SYNE1 in Y hBMMSCs decreased cell regenerative

A Pedigree of the family and segregation analysis of the SYNE1

Subcellular SYNE1 The Human Protein Atlas

Plots for association for combined IoPCAMH cohorts across the SYNE1

Comparison of tumor mutation burden TMB between SYNE1 mutated and

SYNE1 mutations A Graphical overview of the mutations found in this

SYNE1 Exonic Variant rs9479297 Contributes to Concurrent Hepatocellular

SYNE1 antibodies Antibody search engine CiteAb

Tumorinfiltrating immune cells associated with SYNE1 mutation in

SYNE1 Exonic Variant rs9479297 Contributes to Concurrent Hepatocellular

Genetic abnormalities and consequent alterations of protein of SYNE1

Downregulation of SYNE1 in OshCYP7A1 hBMMSCs reduced cell

Pedigree structure clinical features and Sanger sequencing of SYNE1

SYNE1 identified truncating mutations A Sequence traces of healthy

Pedigrees of probands showing segregation of SYNE1 and SYNE2 sequence

Cells from the patient carrying a SYNE1 splice site variant display

SYNE1 Mutation Is Associated with Increased Tumor Mutation Burden and

The positions of the SYNE1 and QK1 mutations Download Scientific Diagram

SYNE1 mutation is associated with increased tumor mutation burden and

Pedigrees of probands showing segregation of SYNE1 and SYNE2 sequence

Tumorinfiltrating immune cells associated with SYNE1 mutation in

SYNE1 Recombinant Rabbit mAbKD

Cerebral MRI features of 6 probands with SYNE1 variants T1 sagittal

Pedigree structure clinical features and Sanger sequencing of SYNE1

Comutation of PCLO and SYNE1 defines an immuneactivated endometrial

SYNE1 mutation may enhance the response to immune checkpoint blockade

Frontiers Identifying SYNE1 Ataxia With Novel Mutations in a Chinese

SYNE1 Mutation Is Associated with Increased Tumor Mutation Burden and

Rs9479297 genotypes associated with SYNE1 expression and patients

Cells from the patient carrying a SYNE1 splice site variant display

Clinical features of a family with a novel SYNE1 mutation a Pedigree

CIZ1 and SYNE1 variants in pedigree 14 and pedigree 8 with BEB A

SYNE1 Gene EmeryDreifuss muscular dystrophy type 4 NGS Genetic Test

SYNE1 Mutation Is Associated with Increased Tumor Mutation Burden and

Clinical features of a family with a novel SYNE1 mutation a Pedigree

SYNE1 mutation may enhance the response to immune checkpoint blockade

SYNE1 antibodies Antibody search engine CiteAb

Tissue expression of SYNE1 Staining in colon The Human Protein Atlas

Pedigree structure clinical features and Sanger sequencing of SYNE1

of the pedigree and genotypes of families with SYNE1 variants

Comutation of PCLO and SYNE1 defines an immuneactivated endometrial

Pedigree structure and Sanger sequencing of SYNE1 variant

Cerebral MRI features of 6 probands with SYNE1 variants T1 sagittal

Figure 1 from Syne1 and Syne2 play crucial roles in myonuclear

Development of the NMJ and the role of Syne1 A Left Motor axons

Cardiovascular Involvement in SYNE Variants A Case Series and

Syne1 A Dystrophin and Klarsichtrelated Protein Associated with

Decitabine Enhances Sorafenib Sensitivity in Renal Cell Carcinoma by

Syne proteins anchor muscle nuclei at the neuromuscular junction PNAS

The location and distribution of 10 variants in a 2D schematic

Syne1 is required for both formation and maintenance of synaptic

Golgi Localization of Syne1 Molecular Biology of the Cell

Identification of nesprin1 variants in DCM patients Mutation

Figure 5 from Genomic mapping and cellular expression of human CPG2

Heterogeneity in clinical features and disease severity in ataxia

Golgi Localization of Syne1 Molecular Biology of the Cell

The generation of Syne1 and Syne2 KASHdomaindeletion mice AB

SUN12 and SyneNesprin12 Complexes Connect Centrosome to the Nucleus

Frontiers DownRegulation of LncCYP7A11 Rejuvenates Aged Human

Schematic diagram for enhancing photosynthesis of Syne and regulating

Specificity Protein 1 Sp1dependent Activation of the Synapsin I Gene

Synapsin 1 General Information Sino Biological

The generation of Syne1 and Syne2 KASHdomaindeletion mice AB

SYNE1QK1 SNPs G G and G E interactions on the risk of

Syne1 A Dystrophin and Klarsichtrelated Protein Associated with

Increased expression of Syne1nesprin1 facilitates nuclear envelope

Extended phenotypes of autosomal recessive cerebellar ataxia type 1

Case Report LateOnset Autosomal Recessive Cerebellar Ataxia

The gene structures of SYNE1 ESR2 and AHNAK Download Scientific Diagram

Analysis of SYNE1 at the DNA and RNA level in AMC patient and control

Golgi Localization of Syne1 Molecular Biology of the Cell

Increased expression of Syne1nesprin1 facilitates nuclear envelope

Circ Res 上海交通大学医学院附属新华医院李毅刚教授团队揭示NUAK1-SYNE1-HERC2-LINC-YAP1轴保护缺血再灌注心肌 ...

Circ Res NUAK1SYNE1HERC2LINCYAP1

Is there a potential role for SyneANC1 in Muscular Dystrophy This

SUN12 and SyneNesprin12 Complexes Connect Centrosome to the Nucleus

Nonsynaptic nuclei are disorganized in Syne1 mice AC A single

Syne1 A Dystrophin and Klarsichtrelated Protein Associated with

A Syn1 hippocampal neurons were transduced at 4 DIV with

CategoryStructural proteins Wikimedia Commons

Golgi Localization of Syne1 Molecular Biology of the Cell

Extended phenotypes of autosomal recessive cerebellar ataxia type 1

Is there a potential role for SyneANC1 in Muscular Dystrophy This

JCI Insight Exome sequencing implicates ancestryrelated Mendelian

Electropherogram of the index patient showing the CC11975G in the

Long noncoding RNANONMMMUT0045522 regulates the unloadinginduced

SYNE16q251 regional association results with five distinct signals

PDF Syne1 and Syne2 play crucial roles In myonuclear anchorage and

SUN12 and SyneNesprin12 complexes connect centrosome to the nucleus

Nesprin1Syne1 ab241403 Abcam

Golgi Localization of Syne1 Molecular Biology of the Cell

Sequence analysis of the SYNE1 transcripts in AMC patient and control

Different types of interaction dendrogram The strongly interacting

Intrafamilial Phenotypic Variability in SYNE1Related Disorder

Circ Res NUAK1SYNE1HERC2LINCYAP1

Familial SYN1 variants related neurodevelopmental disorders in Asian

Increased expression of Syne1nesprin1 facilitates nuclear envelope

Syne1 A Dystrophin and Klarsichtrelated Protein Associated with

Porcine synapsin 1 SYN1 gene analysis and functional characterization

Syne1 A Dystrophin and Klarsichtrelated Protein Associated with

Extended phenotypes of autosomal recessive cerebellar ataxia type 1

SynOne Test CND Life Sciences

SUN12 and SyneNesprin12 Complexes Connect Centrosome to the Nucleus

Synapse analysis using double and triple staining for SYN1 GluNR1 and

Elevated expression of cellular SYNE1 MMP10 and GTPase1 and their

A Syne1 Nup37 Nup43 and Nup188 transcripts were detected in

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