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Volumn 100, Issue 6, 2002, Pages 2145-2152

The immunophenotypic and immunogenotypic B-cell differentiation arrest in bone marrow of RAG-deficient SCID patients corresponds to residual recombination activities of mutated RAG proteins

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN M; RAG1 PROTEIN; RAG2 PROTEIN;

EID: 0037105535     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (77)

References (45)
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    • Primers and protocols for standardized detection of minimal residual disease in acute lymphoblastic leukemia using immunoglobulin and T cell receptor gene rearrangements and TAL1 deletions as PCR targets. Report of the BIOMED-1 Concerted Action: Investigation of minimal residual disease in acute leukemia
    • (1999) Leukemia , vol.13 , pp. 110-118
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    • Flow cytometric diagnosis of the cell lineage and developmental stage of acute lymphoblastic leukemia by novel monoclonal antibodies specific to human pre-B-cell receptor
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  • 42
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    • Mutations in conserved regions of the predicted RAG2 kelch repeats block initiation of V(D)J recombination and result in primary immunodeficiencies
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  • 43
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    • Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome
    • (2001) Blood , vol.97 , pp. 2772-2776
    • Corned, B.1    Moshous, D.2    Gungor, T.3
  • 45
    • 0034662198 scopus 로고    scopus 로고
    • Genetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later stage of pre-B cells in the B-cell differentiation pathway
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.