Skip Header

 

19 results for uniprot:Q0ZCI1Drop in citationmapping

Customize display Download...

Page 1 of 1

Internal IgH class switch region deletions are position-independent and enhanced by AID expression.

Dudley D.D., Manis J.P., Zarrin A.A., Kaylor L., Tian M., Alt F.W.

Proc. Natl. Acad. Sci. U.S.A. 99:9984-9989(2002) GeneRIF 3492 · Mapped (27)
Internal IgH class switch region deletions are position-independent and enhanced by AID expression GeneRIF 3492

The origin of a developmentally regulated Igh replicon is located near the border of regulatory domains for Igh replication and expression.

Zhou J., Ashouian N., Delepine M., Matsuda F., Chevillard C., Riblet R., Schildkraut C.L., Birshtein B.K.

Proc. Natl. Acad. Sci. U.S.A. 99:13693-13698(2002) GeneRIF 3492 · UniProtKB (3) · Mapped (6)
localized an origin of replication in MEL cells to a 3-kb segment located between the 3' Igh regulatory region and Crip GeneRIF 3492

Utilization of Ig heavy chain variable, diversity, and joining gene segments in children with B-lineage acute lymphoblastic leukemia: implications for the mechanisms of VDJ recombination and for pathogenesis.

Dana-Farber Cancer Institute ALL Consortium

Blood 103:4602-4609(2004) GeneRIF 3492 · Mapped (6)
Physical location at the V(H) locus is involved in in different stages of B cell development in b-cell acute lymphoblastic leukemia in children. GeneRIF 3492

Molecular cytogenetic analysis of chromosomal breakpoints in the IGH, MYC, BCL6, and MALT1 gene loci in primary cutaneous B-cell lymphomas.

Hallermann C., Kaune K.M., Gesk S., Martin-Subero J.I., Gunawan B., Griesinger F., Vermeer M.H., Santucci M., Pimpinelli N., Willemze R. et al.

J. Invest. Dermatol. 123:213-219(2004) GeneRIF 3492 · Mapped (23)
Rearrangements of the BCL6 locus were detected in five B-cell lymphomas of the leg and involved IGH (two cases) IGL (one case) and non-IG genes (two cases). GeneRIF 3492

T(3;14)(p14.1;q32) involving IGH and FOXP1 is a novel recurrent chromosomal aberration in MALT lymphoma.

Streubel B., Vinatzer U., Lamprecht A., Raderer M., Chott A.

Leukemia 19:652-658(2005) GeneRIF 3492 · Mapped (18)
This study identifies FOXP1 as a new translocation partner of IGH in a site-dependent subset of MALT lymphomas. GeneRIF 3492

Concurrent translocation of BCL2 and MYC with a single immunoglobulin locus in high-grade B-cell lymphomas.

Knezevich S., Ludkovski O., Salski C., Lestou V., Chhanabhai M., Lam W., Klasa R., Connors J.M., Dyer M.J., Gascoyne R.D. et al.

Leukemia 19:659-663(2005) GeneRIF 3492 · Mapped (18)
frequency and chromosomal features of this der(8)t(8;14;18) in a series of acute leukaemias and malignant lymphomas GeneRIF 3492

Translocation of BCL2 and BCL6 to the same immunoglobulin heavy chain locus in a case of follicular lymphoma.

Rack K., Delannoy A., Ravoet C., Vannuffel P., Hamels J., Gillerot Y.

Leuk. Lymphoma 46:1513-1516(2005) GeneRIF 3492 · Mapped (17)
We present here a case of Follicular Lymphoma with leukemic presentation and a complex translocation involving the IgH BCL2 and BCL6 loci GeneRIF 3492

BCL-2/IgH translocation in peripheral blood cells of healthy Chinese individuals of Han nationality located in Zhejiang area.

Liang Y., Zhou R., Ye Y.F., Xie Y., Mao Z.R.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 22:548-550(2005) GeneRIF 3492 · Mapped (10)
The low frequency of BCL-2/IgH translocation in healthy Chinese individuals of Han nationality located in Zhejiang area may be one of the reasons for the difference in the incidence of follicular lymphoma between China and Western countries. GeneRIF 3492

t(6;14)(p22;q32): a new recurrent IGH@ translocation involving ID4 in B-cell precursor acute lymphoblastic leukemia (BCP-ALL).

Russell L.J., Akasaka T., Majid A., Sugimoto K.J., Loraine Karran E., Nagel I., Harder L., Claviez A., Gesk S., Moorman A.V. et al.

Blood 111:387-391(2008) GeneRIF 3492 · Mapped (6)
translocation t(6;14)(p22;q32) involving IGH@ as a novel recurrent translocation in 13 b-cell precursor acute lymphoblastic leukemia patients GeneRIF 3492

Association of t(14;18) translocation with HCV infection in gastrointestinal MALT lymphomas.

Libra M., Gloghini A., Malaponte G., Gangemi P., De Re V., Cacopardo B., Spandidos D.A., Nicoletti F., Stivala F., Zignego A.L. et al.

J. Hepatol. 49:170-174(2008) GeneRIF 3492 · Mapped (10)
among gastrointestinal MALT lymphomas t(14;18)-(IgH;Bcl-2) translocation clusters in hepatitis C-positive patients sustaining the role of HCV infection in the lymphoma development GeneRIF 3492

Novel IGHalpha translocations, t(2;14)(q14.3;q32) and t(14;17)(q32;q21), in B-cell precursor acute lymphoblastic leukemia.

Aventin A., Sanchez J., Nomdedeu J.F., Estany C., Forcada P., La Starza R., Mecucci C.

Cancer Genet. Cytogenet. 185:57-59(2008) GeneRIF 3492 · Mapped (6)
Novel IGH translocations t(2;14)(q14.3;q2) and t(14;17)(q32;q21) in B-cell precursor acute lymphoblastic leukemia are reported. GeneRIF 3492

Serum bactericidal activity against Neisseria meningitidis in patients with C3 nephritic factors is dependent on IgG allotypes.

Skattum L., Gullstrand B., Holmstrom E., Oxelius V.A., Truedsson L.

Clin. Immunol. 129:123-131(2008) GeneRIF 3492 · Mapped (6)
IGHG genotype is important in defense against meningococci in individuals with low complement function and possibly in combination with other immunodeficiencies. GeneRIF 3492

A novel translocation, t(14;19)(q32;p13), involving IGH@ and the cytokine receptor for erythropoietin.

Russell L.J., De Castro D.G., Griffiths M., Telford N., Bernard O., Panzer-Grumayer R., Heidenreich O., Moorman A.V., Harrison C.J.

Leukemia 23:614-617(2009) GeneRIF 3492 · Mapped (8)
2 BCP-ALL patients had a novel recurrent reciprocal translocation involving IGH@ & EPOR. EPOR mRNA expression was increased at diagnosis and relapse. GeneRIF 3492

JAK2V617F-positive essential thrombocythemia and multiple myeloma with IGH/CCND1 gene translocation coexist, but originate from separate clones.

Kuroda J., Matsumoto Y., Tanaka R., Kurita K., Kobayashi T., Shimizu D., Kimura S., Ashihara E., Horiike S., Shimazaki C. et al.

Acta Haematol. 120:177-181(2008) GeneRIF 3492 · Mapped (18)
JAK2V617F-positive essential thrombocythemia and multiple myeloma with IGH/CCND1 gene translocation coexist but originate from separate clones GeneRIF 3492

Splenic marginal zone lymphoma: Clinical clustering of immunoglobulin heavy chain repertoires.

Arcaini L., Zibellini S., Passamonti F., Rattotti S., Lucioni M., Invernizzi R., Merli M., Rizzi S., Boveri E., Rumi E. et al.

Blood Cells Mol. Dis. 42:286-291(2009) GeneRIF 3492 · Mapped (6)
IGHV rearrangement analysis in splenic marginal zone B-cell lymphoma reveals a non-random preference for use of IGHV1-2 IGHV3-23 and IGHV3-30 genes whose presence differs according to clinical features and prognostic category. GeneRIF 3492

Frequency of 5'IGH deletions in B-cell chronic lymphocytic leukemia.

Quintero-Rivera F., Nooraie F., Rao P.N.

Cancer Genet. Cytogenet. 190:33-39(2009) GeneRIF 3492 · Mapped (6)
Deletion of 5'IGH corresponding to the variable IGH segment (IGH(V)) was the most recurrent aberration observed in 82% (the second most common finding among our patients). GeneRIF 3492

Chronic lymphocytic leukemia With t(2;14)(p16;q32) involves the BCL11A and IgH genes and is associated with atypical morphologic features and unmutated IgVH genes.

Yin C.C., Lin K.I., Ketterling R.P., Knudson R.A., Medeiros L.J., Barron L.L., Huh Y.O., Luthra R., Keating M.J., Abruzzo L.V.

Am. J. Clin. Pathol. 131:663-670(2009) GeneRIF 3492 · Mapped (14)
Chronic lymphocytic leukemia With t(2;14)(p16;q32) involves the BCL11A and IgH genes and is associated with atypical morphologic features and unmutated IgVH genes. GeneRIF 3492

Mutation analysis of IgVH genes in splenic marginal zone lymphomas: correlation with clinical characteristics and outcome.

Kalpadakis C., Pangalis G.A., Dimitriadou E., Angelopoulou M.K., Siakantaris M.P., Kyrtsonis M.C., Ximeris M., Tzenou T., Sahanas S., Yiakoumis X. et al.

Anticancer Res. 29:1811-1816(2009) GeneRIF 3492 · Mapped (6)
significant fraction of splenic marginal zone lymphomas derive from naive B-cells with unmutated IgVH genes indicating heterogeneous group of diseases with respect to cell origin; prognostic significance of mutation status was not observed in this study GeneRIF 3492

Identification of the gene encoding cyclin E1 (CCNE1) as a novel IGH translocation partner in t(14;19)(q32;q12) in diffuse large B-cell lymphoma.

Nagel I., Akasaka T., Klapper W., Gesk S., Bottcher S., Ritgen M., Harder L., Kneba M., Dyer M.J., Siebert R.

Haematologica 94:1020-1023(2009) GeneRIF 3492 · Mapped (6)
CCNE1 is a novel IGH translocation partner in t(14;19)(q32;q12) in diffuse large B-cell lymphoma GeneRIF 3492

Page 1 of 1