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Nuclear pore complex protein RANBP2 and related SUMOylation in solid malignancies

Genes & diseases, 2024-09, p.101407, Article 101407

2024

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Antibody-assisted selective isolation of Purkinje cell nuclei from mouse cerebellar tissue

Cell reports methods, 2024-07, Vol.4 (7), p.100816, Article 100816

2024

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OP-068 Case report of RANBP2 mutation and familial acute necrotizing encephalopathy

BMJ paediatrics open, 2024-07, Vol.8 (Suppl 5), p.A31-A32

Dhariwal, Kuldeep

2024

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Association of RAN and RANBP2 Gene Polymorphisms With Glioma Susceptibility in Chinese Children

Cancer reports, 2024-07, Vol.7 (7), p.e2136-n/a

2024

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Proteostatic Remodeling of Small Heat Shock ChaperonesCrystallins by Ran-Binding Protein 2and the Peptidyl-Prolyl cis–trans Isomerase and Chaperone Activities of Its Cyclophilin Domain

ACS chemical neuroscience, 2024-05, Vol.15 (10), p.1967-1989

2024

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A 5-year-old boy with super-refractory status epilepticus and RANBP2 variant warranting life-saving hemispherotomy

Epilepsia open, 2024-02, Vol.9 (1), p.424-431

2024

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RanBP2/Nup358 Mediates Sumoylation of STAT1 and Antagonizes Interferon-α-Mediated Antiviral Innate Immunity

International journal of molecular sciences, 2023-12, Vol.25 (1), p.299

2023

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Recurrent infection triggered encephalopathy syndrome in a pediatric patient with RANBP2 mutation and severe acute respiratory syndrome coronavirus 2 infection

Pediatric investigation, 2023-12, Vol.7 (4), p.290-296

2023

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Cellular gp96 upregulates AFP expression by blocking NR5A2 SUMOylation and ubiquitination in hepatocellular carcinoma

Journal of molecular cell biology, 2023-11, Vol.15 (5)

2023

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Rapid and inexpensive bedside diagnosis of RAN binding protein 2-associated acute necrotizing encephalopathy

Frontiers in neurology, 2023-11, Vol.14, p.1282059

2023

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Acute necrotizing encephalopathy associated with COVID-19: case series and systematic review

Journal of neurology, 2023-11, Vol.270 (11), p.5171-5181

2023

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Distinct Mitotic Functions of Nucleolar and Spindle-Associated Protein 1 (NuSAP1) Are Controlled by Two Consensus SUMOylation Sites

Cells (Basel, Switzerland), 2023-10, Vol.12 (21), p.2545

2023

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The Clinical, Laboratory, Etiological Profile and Outcome of Acute Necrotizing Encephalitis of Childhood (ANEC) in Tertiary Care Centre from Southern India

Journal of pediatric neurology, 2023-10, Vol.21 (5), p.341-346

2023

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The magnified view: from ancient trinkets to single nuclear pore complexes

FEBS letters, 2023-10, Vol.597 (20), p.2590-2596

2023

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RANBP2 evolution and human disease

FEBS letters, 2023-10, Vol.597 (20), p.2519-2533

2023

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Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

Genetics in medicine, 2023-09, Vol.25 (9), p.100897-100897, Article 100897

2023

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Phosphoproteomics Reveal New Candidates in Abnormal Spermatogenesis of Pseudomales in Cynoglossus semilaevis

International journal of molecular sciences, 2023-07, Vol.24 (14), p.11430

2023

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De novo RANBP2 variant in a fetal demise case with cerebral intraparenchymal hemorrhage

American journal of medical genetics. Part A, 2023-07, Vol.191 (7), p.1973-1977

2023

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Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention

Acta neurologica Belgica, 2023-04, Vol.123 (2), p.571-582

2023

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Aurora B SUMOylation Is Restricted to Centromeres in Early Mitosis and Requires RANBP2

Cells (Basel, Switzerland), 2023-01, Vol.12 (3), p.372

2023

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Pediatric recurrent acute necrotizing encephalomyelitis, RANBP2 genotype and Sars-CoV-2 infection: Diagnosis, pathogenesis and targeted treatments from a case study

European journal of paediatric neurology, 2023-01, Vol.42, p.117-121

2023

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Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy

Nucleus (Austin, Tex.), 2022-12, Vol.13 (1), p.156-171

2022

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In vitro characterization of the full-length human dynein-1 cargo adaptor BicD2

Structure (London), 2022-11, Vol.30 (11), p.1470-1478.e3

2022

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First case with RANBP2 biallelic mutation and severe acute necrotizing encephalopathy phenotype

Clinical neurology and neurosurgery, 2022-10, Vol.221, p.107418, Article 107418

2022

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COVID-19 related acute necrotizing encephalopathy with extremely high interleukin-6 and RANBP2 mutation in a patient with recently immunized inactivated virus vaccine and no pulmonary involvement

BMC infectious diseases, 2022-07, Vol.22 (1), p.1-640, Article 640

2022

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Nuclear pore complex protein RANBP2 and related SUMOylation in solid malignancies

Antibody-assisted selective isolation of Purkinje cell nuclei from mouse cerebellar tissue

OP-068 Case report of RANBP2 mutation and familial acute necrotizing encephalopathy

Association of RAN and RANBP2 Gene Polymorphisms With Glioma Susceptibility in Chinese Children

Proteostatic Remodeling of Small Heat Shock ChaperonesCrystallins by Ran-Binding Protein 2and the Peptidyl-Prolyl cis–trans Isomerase and Chaperone Activities of Its Cyclophilin Domain

A 5-year-old boy with super-refractory status epilepticus and RANBP2 variant warranting life-saving hemispherotomy

RanBP2/Nup358 Mediates Sumoylation of STAT1 and Antagonizes Interferon-α-Mediated Antiviral Innate Immunity

Recurrent infection triggered encephalopathy syndrome in a pediatric patient with RANBP2 mutation and severe acute respiratory syndrome coronavirus 2 infection

Cellular gp96 upregulates AFP expression by blocking NR5A2 SUMOylation and ubiquitination in hepatocellular carcinoma

Rapid and inexpensive bedside diagnosis of RAN binding protein 2-associated acute necrotizing encephalopathy

Acute necrotizing encephalopathy associated with COVID-19: case series and systematic review

Distinct Mitotic Functions of Nucleolar and Spindle-Associated Protein 1 (NuSAP1) Are Controlled by Two Consensus SUMOylation Sites

The Clinical, Laboratory, Etiological Profile and Outcome of Acute Necrotizing Encephalitis of Childhood (ANEC) in Tertiary Care Centre from Southern India

The magnified view: from ancient trinkets to single nuclear pore complexes

RANBP2 evolution and human disease

Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

Phosphoproteomics Reveal New Candidates in Abnormal Spermatogenesis of Pseudomales in Cynoglossus semilaevis

De novo RANBP2 variant in a fetal demise case with cerebral intraparenchymal hemorrhage

Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention

Aurora B SUMOylation Is Restricted to Centromeres in Early Mitosis and Requires RANBP2

Pediatric recurrent acute necrotizing encephalomyelitis, RANBP2 genotype and Sars-CoV-2 infection: Diagnosis, pathogenesis and targeted treatments from a case study

Workshop on RanBP2/Nup358 and acute necrotizing encephalopathy

In vitro characterization of the full-length human dynein-1 cargo adaptor BicD2

First case with RANBP2 biallelic mutation and severe acute necrotizing encephalopathy phenotype

COVID-19 related acute necrotizing encephalopathy with extremely high interleukin-6 and RANBP2 mutation in a patient with recently immunized inactivated virus vaccine and no pulmonary involvement

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