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Analysis of vector genome integrations in multicentric lymphoma after AAV gene therapy in a severe hemophilia A dog

Molecular Therapy — Methods & Clinical Development(2023)10.1016/j.omtm.2023.101159Source: DataRank Database

Analysis of vector genome integrations in multicentric lymphoma after AAV gene therapy in a severe hemophilia A dog is a research paper published in Molecular Therapy — Methods & Clinical Development (2023). On theSindex it has a DataRank of 0. It has been cited 8 times.

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Open Access8 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (13 grants)Impact (FWCI 1.69)OA: goldTopics (25)IDs (PubMed, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (11)

Bhavya S. Doshi ORCID,Elinor Willis ORCID,Timothy C. Nichols ORCID,Emma Cook ORCID,J.K. Everett ORCID

Live enrichment

PubMed:38094200 OpenAlex:https://openalex.org/W4388673135

University of Pennsylvania

Grant: HL07439

National Heart, Lung, and Blood Institute

Grant: HL158781

National Heart, Lung, and Blood Institute

Grant: N01_7N92019D00041

National Institutes of Health

Grant: 5UM1AI164570-03

BEAT-HIV: Delaney Collaboratory to Cure HIV-1 Infection by Combination Immunotherapy

National Institutes of Health

Grant: 4U01AI125051-07

Gene Therapy for SCID-X1 with Low Dose Busulfan and a SIN-lentiviral Vector

National Institutes of Health

Grant: 5R01CA241762-05

Linking insertional mutagenesis and cell function to improve CAR T cell therapy

National Institutes of Health

Grant: 1R01HL142791-01A1

A Phase I Clinical Trial Testing Feasibility of Hematopoietic Stem Cell Gene Therapy Using Platelet Factor VIII to Safely Improve Hemostasis for Severe Hemophilia A with Inhibitory Antibodies

National Institutes of Health

Grant: 5T32HL007439-37

Hematology Clinical Research Training Program

National Institutes of Health

Grant: 2P30CA016520-35

Abramson Cancer Center Support Grant

National Institutes of Health

Grant: 5U19AI149680-03

Engineering T cells to Provide Durable Control of HIV-1 Replication

National Institutes of Health

Grant: 5R01HL158781-03

Immune tolerance induction by AAV-FVIII gene therapy for canine hemophilia A with inhibitors

National Institutes of Health

Grant: 5P30AI045008-10

Core--Immunology Facility

National Institutes of Health

Grant: 5R01HL160748-02

Preserving Genome Integrity In AAV-Mediated Gene Therapy

FWCI

1.69

Citation Percentile

0.9%

Citation Trend

2024

2025

2026

goldLicense: cc-by-nc-nd

journalhttps://doi.org/10.1016/j.omtm.2023.101159

publisherhttps://doi.org/10.1016/j.omtm.2023.101159

publisherhttps://api.elsevier.com/content/article/PII:S2329050123001985?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2329050123001985?httpAccept=text/plain

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38094200

Fields of Study

Virus-based gene therapy researchViral Infectious Diseases and Gene Expression in InsectsVector-Borne Animal Diseases0301 basic medicine03 medical and health sciences

Keywords

Genetic enhancementVector (molecular biology)VirologyLymphomaMedicineGenomeGeneComputational biologyBiologyInternal medicineGeneticsQH573-671genotoxicitycancerAAVintegrationOriginal ArticleQH426-470Cytologygene therapy

Sustainable Development Goals

SDG 0: Zero hunger