Dupain C, Harttrampf A, Urbinati G, Geoerger B, Massaad-Massade L
Mol Ther Nucleic Acids. 2017; 6:315-326.
PMID: 28325298
PMC: 5363511.
DOI: 10.1016/j.omtn.2017.01.005.
Smith C
Oncogene. 2016; 36(15):2045-2053.
PMID: 27669440
PMC: 5395699.
DOI: 10.1038/onc.2016.343.
Schlegelberger B
Mol Cytogenet. 2013; 6(1):20.
PMID: 23693023
PMC: 3660208.
DOI: 10.1186/1755-8166-6-20.
Toyota S, Nakamura N, Dan K
Int J Hematol. 2005; 81(1):66-8.
PMID: 15717692
DOI: 10.1532/ijh97.04129.
Toyota S, Nakamura N, Dan K
Int J Hematol. 2002; 75(3):314-7.
PMID: 11999363
DOI: 10.1007/BF02982049.
Mantle cell lymphoma is characterized by inactivation of the ATM gene.
Schaffner C, Idler I, Stilgenbauer S, Dohner H, Lichter P
Proc Natl Acad Sci U S A. 2000; 97(6):2773-8.
PMID: 10706620
PMC: 16005.
DOI: 10.1073/pnas.050400997.
Inversion (14)(q12qter) or (q11.2q32.3): the most frequently acquired rearrangement in lymphocytes.
Aurias A, Couturier J, Dutrillaux A, Dutrillaux B, Herpin F, Lamoliatte E
Hum Genet. 1985; 71(1):19-21.
PMID: 4029952
DOI: 10.1007/BF00295660.
New data on clonal anomalies of chromosome 14 in ataxia telangiectasia: tct(14;14) and inv(14).
Aurias A, Croquette M, NUYTS J, Griscelli C, Dutrillaux B
Hum Genet. 1986; 72(1):22-4.
PMID: 3943860
DOI: 10.1007/BF00278811.
Molecular cloning of a DNA fragment from human chromosome 14(14q11) involved in T-cell malignancies.
Caubet J, Bernheim A, Mauchauffe M, Palmer E, Berger R, Larsen C
EMBO J. 1985; 4(13A):3427-33.
PMID: 3912169
PMC: 554680.
DOI: 10.1002/j.1460-2075.1985.tb04100.x.
The chromosomal location of T-cell receptor genes and a T cell rearranging gene: possible correlation with specific translocations in human T cell leukaemia.
Rabbitts T, Lefranc M, Stinson M, Sims J, Schroder J, Steinmetz M
EMBO J. 1985; 4(6):1461-5.
PMID: 3875483
PMC: 554368.
DOI: 10.1002/j.1460-2075.1985.tb03803.x.
T cell receptor alpha chain genes are located on chromosome 14 at 14q11-14q12 in humans.
Caccia N, BRUNS G, Kirsch I, Hollis G, Bertness V, Mak T
J Exp Med. 1985; 161(5):1255-60.
PMID: 3872924
PMC: 2187598.
DOI: 10.1084/jem.161.5.1255.
Cytogenetic markers in hematoproliferative disorders.
Fonatsch C
Blut. 1985; 51(5):315-28.
PMID: 3864500
DOI: 10.1007/BF00320042.
DNA rearrangements in human B- and T-cell malignancies.
Smith C, Hammarstrom L
Med Oncol Tumor Pharmacother. 1986; 3(3-4):153-7.
PMID: 3543528
DOI: 10.1007/BF02934991.
T-cell receptor alpha-chain gene is split in a human T-cell leukemia cell line with a t(11;14)(p15;q11).
Le Beau M, McKeithan T, Shima E, Chan S, Bell G, Rowley J
Proc Natl Acad Sci U S A. 1986; 83(24):9744-8.
PMID: 3540949
PMC: 387217.
DOI: 10.1073/pnas.83.24.9744.
Molecular cloning of the breakpoint junction of a human chromosomal 8;14 translocation involving the T-cell receptor alpha-chain gene and sequences on the 3' side of MYC.
McKeithan T, Shima E, Le Beau M, Minowada J, Rowley J, Diaz M
Proc Natl Acad Sci U S A. 1986; 83(17):6636-40.
PMID: 3529089
PMC: 386559.
DOI: 10.1073/pnas.83.17.6636.
Gene encoding the alpha chain of the T-cell receptor is moved immediately downstream of c-myc in a chromosomal 8;14 translocation in a cell line from a human T-cell leukemia.
Shima E, Le Beau M, McKeithan T, Minowada J, Showe L, Mak T
Proc Natl Acad Sci U S A. 1986; 83(10):3439-43.
PMID: 3517860
PMC: 323530.
DOI: 10.1073/pnas.83.10.3439.
Growth of large chromosomally abnormal T cell clones in ataxia telangiectasia patients is associated with translocation at 14q11. A model for other T cell neoplasia.
Hollis R, Kennaugh A, Butterworth S, Taylor A
Hum Genet. 1987; 76(4):389-95.
PMID: 3497086
DOI: 10.1007/BF00272451.
A subpopulation of t(2;14)(p11;q32) cells in ataxia telangiectasia B lymphocytes.
Butterworth S, Taylor A
Hum Genet. 1986; 73(4):346-9.
PMID: 3488948
DOI: 10.1007/BF00279098.
The chromosome breakpoint at 14q32 in an ataxia telangiectasia t(14;14) T cell clone is different from the 14q32 breakpoint in Burkitts and an inv(14) T cell lymphoma.
Kennaugh A, Butterworth S, Hollis R, Baer R, Rabbitts T, Taylor A
Hum Genet. 1986; 73(3):254-9.
PMID: 3488254
DOI: 10.1007/BF00401239.
T-lymphocytes with 7;14 translocations: frequency of occurrence, breakpoints, and clinical and biological significance.
Dewald G, Noonan K, Spurbeck J, Johnson D
Am J Hum Genet. 1986; 38(4):520-32.
PMID: 3486591
PMC: 1684808.