152 related articles for article (PubMed ID: 15829267)
1. Adult lupus-prone MRL/MpJ2+ mice express a primary antibody repertoire that differs in CDR-H3 length distribution and hydrophobicity from that expressed in the C3H parental strain.
Zemlin M; Ippolito GC; Zemlin C; Link J; Monestier M; Schroeder HW
Mol Immunol; 2005 May; 42(7):789-98. PubMed ID: 15829267
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Heavy chain revision in MRL mice: a potential mechanism for the development of autoreactive B cell precursors.
Klonowski KD; Monestier M
J Immunol; 2000 Oct; 165(8):4487-93. PubMed ID: 11035088
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. The CDR-H3 repertoire from TdT-deficient adult bone marrow is a close, but not exact, homologue of the CDR-H3 repertoire from perinatal liver.
Schelonka RL; Ivanov II; Vale AM; Szymanska E; Zemlin M; Gartland GL; Schroeder HW
J Immunol; 2010 Nov; 185(10):6075-84. PubMed ID: 20956348
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Categorical selection of the antibody repertoire in splenic B cells.
Schelonka RL; Tanner J; Zhuang Y; Gartland GL; Zemlin M; Schroeder HW
Eur J Immunol; 2007 Apr; 37(4):1010-21. PubMed ID: 17345580
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Fundamental characteristics of the expressed immunoglobulin VH and VL repertoire in different canine breeds in comparison with those of humans and mice.
Steiniger SC; Dunkle WE; Bammert GF; Wilson TL; Krishnan A; Dunham SA; Ippolito GC; Bainbridge G
Mol Immunol; 2014 May; 59(1):71-8. PubMed ID: 24509215
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Repertoire Analysis of Antibody CDR-H3 Loops Suggests Affinity Maturation Does Not Typically Result in Rigidification.
Jeliazkov JR; Sljoka A; Kuroda D; Tsuchimura N; Katoh N; Tsumoto K; Gray JJ
Front Immunol; 2018; 9():413. PubMed ID: 29545810
[TBL] [Abstract][Full Text] [Related]
15. DH and JH usage in murine fetal liver mirrors that of human fetal liver.
Schelonka RL; Szymanska E; Vale AM; Zhuang Y; Gartland GL; Schroeder HW
Immunogenetics; 2010 Oct; 62(10):653-66. PubMed ID: 20714894
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Forced usage of positively charged amino acids in immunoglobulin CDR-H3 impairs B cell development and antibody production.
Ippolito GC; Schelonka RL; Zemlin M; Ivanov II; Kobayashi R; Zemlin C; Gartland GL; Nitschke L; Pelkonen J; Fujihashi K; Rajewsky K; Schroeder HW
J Exp Med; 2006 Jun; 203(6):1567-78. PubMed ID: 16754718
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Structural classification of CDR-H3 revisited: a lesson in antibody modeling.
Kuroda D; Shirai H; Kobori M; Nakamura H
Proteins; 2008 Nov; 73(3):608-20. PubMed ID: 18473362
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
