182 related articles for article (PubMed ID: 29944758)
1. The sequences encoded by immunoglobulin diversity (D
Khass M; Vale AM; Burrows PD; Schroeder HW
Immunol Rev; 2018 Jul; 284(1):106-119. PubMed ID: 29944758
[TBL] [Abstract][Full Text] [Related]
2. HIV-1 gp140 epitope recognition is influenced by immunoglobulin DH gene segment sequence.
Wang Y; Kapoor P; Parks R; Silva-Sanchez A; Alam SM; Verkoczy L; Liao HX; Zhuang Y; Burrows P; Levinson M; Elgavish A; Cui X; Haynes BF; Schroeder H
Immunogenetics; 2016 Feb; 68(2):145-55. PubMed ID: 26687685
[TBL] [Abstract][Full Text] [Related]
3. Violation of an evolutionarily conserved immunoglobulin diversity gene sequence preference promotes production of dsDNA-specific IgG antibodies.
Silva-Sanchez A; Liu CR; Vale AM; Khass M; Kapoor P; Elgavish A; Ivanov II; Ippolito GC; Schelonka RL; Schoeb TR; Burrows PD; Schroeder HW
PLoS One; 2015; 10(2):e0118171. PubMed ID: 25706374
[TBL] [Abstract][Full Text] [Related]
4. Preferential use of DH reading frame 2 alters B cell development and antigen-specific antibody production.
Schelonka RL; Zemlin M; Kobayashi R; Ippolito GC; Zhuang Y; Gartland GL; Szalai A; Fujihashi K; Rajewsky K; Schroeder HW
J Immunol; 2008 Dec; 181(12):8409-15. PubMed ID: 19050258
[TBL] [Abstract][Full Text] [Related]
5. Replacement of TCR Dβ With Immunoglobulin D
Levinson M; Khass M; Burrows PD; Schroeder HW
Front Immunol; 2020; 11():573413. PubMed ID: 33133088
[TBL] [Abstract][Full Text] [Related]
6. Development of the expressed Ig CDR-H3 repertoire is marked by focusing of constraints in length, amino acid use, and charge that are first established in early B cell progenitors.
Ivanov II; Schelonka RL; Zhuang Y; Gartland GL; Zemlin M; Schroeder HW
J Immunol; 2005 Jun; 174(12):7773-80. PubMed ID: 15944280
[TBL] [Abstract][Full Text] [Related]
7. Alterations in B cell development, CDR-H3 repertoire and dsDNA-binding antibody production among C57BL/6 ΔD-iD mice congenic for the lupus susceptibility loci sle1, sle2 or sle3.
Khass M; Schelonka RL; Liu CR; Elgavish A; Morel L; Burrows PD; Schroeder HW
Autoimmunity; 2017 Feb; 50(1):42-51. PubMed ID: 28166678
[TBL] [Abstract][Full Text] [Related]
8. Recirculating bone marrow B cells in C57BL/6 mice are more tolerant of highly hydrophobic and highly charged CDR-H3s than those in BALB/c mice.
Khass M; Buckley K; Kapoor P; Schelonka RL; Watkins LS; Zhuang Y; Schroeder HW
Eur J Immunol; 2013 Mar; 43(3):629-40. PubMed ID: 23225217
[TBL] [Abstract][Full Text] [Related]
9. In the Absence of Central pre-B Cell Receptor Selection, Peripheral Selection Attempts to Optimize the Antibody Repertoire by Enriching for CDR-H3 Y101.
Khass M; Blackburn T; Elgavish A; Burrows PD; Schroeder HW
Front Immunol; 2018; 9():120. PubMed ID: 29472919
[TBL] [Abstract][Full Text] [Related]
10. Genetic control of DH reading frame and its effect on B-cell development and antigen-specifc antibody production.
Schroeder HW; Zemlin M; Khass M; Nguyen HH; Schelonka RL
Crit Rev Immunol; 2010; 30(4):327-44. PubMed ID: 20666706
[TBL] [Abstract][Full Text] [Related]
11. Preimmune Control of the Variance of TCR CDR-B3: Insights Gained From Germline Replacement of a TCR Dβ Gene Segment With an Ig D
Khass M; Levinson M; Schelonka RL; Kapoor P; Burrows PD; Schroeder HW
Front Immunol; 2020; 11():2079. PubMed ID: 33042119
[TBL] [Abstract][Full Text] [Related]
12. The restricted DH gene reading frame usage in the expressed human antibody repertoire is selected based upon its amino acid content.
Benichou J; Glanville J; Prak ET; Azran R; Kuo TC; Pons J; Desmarais C; Tsaban L; Louzoun Y
J Immunol; 2013 Jun; 190(11):5567-77. PubMed ID: 23630353
[TBL] [Abstract][Full Text] [Related]
13. Despite extensive similarity in germline DH and JH sequence, the adult Rhesus macaque CDR-H3 repertoire differs from human.
Link JM; Larson JE; Schroeder HW
Mol Immunol; 2005 May; 42(8):943-55. PubMed ID: 15829286
[TBL] [Abstract][Full Text] [Related]
14. A single DH gene segment creates its own unique CDR-H3 repertoire and is sufficient for B cell development and immune function.
Schelonka RL; Ivanov II; Jung DH; Ippolito GC; Nitschke L; Zhuang Y; Gartland GL; Pelkonen J; Alt FW; Rajewsky K; Schroeder HW
J Immunol; 2005 Nov; 175(10):6624-32. PubMed ID: 16272317
[TBL] [Abstract][Full Text] [Related]
15. Expressed murine and human CDR-H3 intervals of equal length exhibit distinct repertoires that differ in their amino acid composition and predicted range of structures.
Zemlin M; Klinger M; Link J; Zemlin C; Bauer K; Engler JA; Schroeder HW; Kirkham PM
J Mol Biol; 2003 Dec; 334(4):733-49. PubMed ID: 14636599
[TBL] [Abstract][Full Text] [Related]
16. The role of evolutionarily conserved germ-line DH sequence in B-1 cell development and natural antibody production.
Vale AM; Nobrega A; Schroeder HW
Ann N Y Acad Sci; 2015 Dec; 1362(1):48-56. PubMed ID: 26104486
[TBL] [Abstract][Full Text] [Related]
17. Germline-enforced enrichment for charged amino acids in TCR beta chain (TCRβ) complementarity determining region 3 (CDR-B3) alters T cell development, repertoire content, and antigen recognition.
Levinson M; Khass M; Burrows PD; Schroeder HW
Immunogenetics; 2023 Aug; 75(4):341-353. PubMed ID: 37119386
[TBL] [Abstract][Full Text] [Related]
18. CDR-H3 diversity is not required for antigen recognition by synthetic antibodies.
Persson H; Ye W; Wernimont A; Adams JJ; Koide A; Koide S; Lam R; Sidhu SS
J Mol Biol; 2013 Feb; 425(4):803-11. PubMed ID: 23219464
[TBL] [Abstract][Full Text] [Related]
19. Regulation of repertoire development through genetic control of DH reading frame preference.
Zemlin M; Schelonka RL; Ippolito GC; Zemlin C; Zhuang Y; Gartland GL; Nitschke L; Pelkonen J; Rajewsky K; Schroeder HW
J Immunol; 2008 Dec; 181(12):8416-24. PubMed ID: 19050259
[TBL] [Abstract][Full Text] [Related]
20. Dynamics of heavy chain junctional length biases in antibody repertoires.
Sankar K; Hoi KH; Hötzel I
Commun Biol; 2020 May; 3(1):207. PubMed ID: 32358517
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
