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Literature DB >> 11269227

Primary T-lymphocyte immunodeficiencies.

A Fischer¹.

Abstract

Entities: Disease

Mesh：

Year: 2001 PMID： 11269227 DOI： 10.1385/CRIAI:20:1:3

Source DB: PubMed Journal: Clin Rev Allergy Immunol ISSN： 1080-0549 Impact factor: 8.667

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121 in total

1. A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients.

Authors: K Masternak; E Barras; M Zufferey; B Conrad; G Corthals; R Aebersold; J C Sanchez; D F Hochstrasser; B Mach; W Reith
Journal: Nat Genet Date: 1998-11 Impact factor: 38.330

2. Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency.

Authors: M E Conley; A Lavoie; C Briggs; P Brown; C Guerra; J M Puck
Journal: Proc Natl Acad Sci U S A Date: 1988-05 Impact factor: 11.205

3. Limited T cell receptor diversity of transplacentally acquired maternal T cells in severe combined immunodeficiency.

Authors: C Knobloch; S F Goldmann; W Friedrich
Journal: J Immunol Date: 1991-06-15 Impact factor: 5.422

4. Nonsense mutation at Tyr-4046 in the DNA-dependent protein kinase catalytic subunit of severe combined immune deficiency mice.

Authors: R Araki; A Fujimori; K Hamatani; K Mita; T Saito; M Mori; R Fukumura; M Morimyo; M Muto; M Itoh; K Tatsumi; M Abe
Journal: Proc Natl Acad Sci U S A Date: 1997-03-18 Impact factor: 11.205

10. Preferential utilization of the immature JH segment and absence of somatic mutation in the CDR3 junction of the Ig H chain gene in three X-linked severe combined immunodeficiency patients.

Authors: Y Minegishi; H Okawa; K Sugamura; J Yata
Journal: Int Immunol Date: 1994-11 Impact factor: 4.823

1 in total

1. Hematopoietic cell transplantation for treatment of primary immune deficiencies.

Authors: Lauri Burroughs; Ann Woolfrey
Journal: Cell Ther Transplant Date: 2010-08-31

1 in total

Primary T-lymphocyte immunodeficiencies.

1. A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients.

2. Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency.

3. Limited T cell receptor diversity of transplacentally acquired maternal T cells in severe combined immunodeficiency.

4. Nonsense mutation at Tyr-4046 in the DNA-dependent protein kinase catalytic subunit of severe combined immune deficiency mice.

5. Treatment of X-linked severe combined immunodeficiency by in utero transplantation of paternal bone marrow.

6. Normal T cell receptor V beta usage in a primary immunodeficiency associated with HLA class II deficiency.

7. Interaction of IL-2R beta and gamma c chains with Jak1 and Jak3: implications for XSCID and XCID.

Review 8. DNA double-strand break repair and V(D)J recombination: involvement of DNA-PK.

9. Mismatched bone marrow transplantation for Omenn syndrome: a variant of severe combined immunodeficiency.

10. Preferential utilization of the immature JH segment and absence of somatic mutation in the CDR3 junction of the Ig H chain gene in three X-linked severe combined immunodeficiency patients.

1. Hematopoietic cell transplantation for treatment of primary immune deficiencies.