##   query.q: KMT2A-MLLT1
##   query.defType: edismax
##   query.indent: True
##   query.qf: ac^16 id^16 sy^8 text
##   query.fl: ac
##   query.pf: ac^160 id^160 sy^80 text
##   query.start: 0
##   query.q.op: AND
##   query.sort: score desc
##   query.rows: 1000
##   query.wt: json
##   query.fields: (None)
##   query.format: txt
##   QTime: 1
##   response.numFound: 11

ID   M9-ENL1
AC   CVCL_A8IE
SY   M9 ENL1; M9ENL1
DR   GEO; GSM838434
DR   GEO; GSM838435
DR   GEO; GSM838436
DR   Wikidata; Q107115912
RX   PubMed=22160482;
CC   Characteristics: Expresses a transfected KMT2A-MLLT1 (MLL-ENL) fusion protein. Mimics the features of primary human pro-B cell acute lymphoblastic leukemia (PubMed=22160482).
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:7132; KMT2A (Note=KMT2A-MLLT1 fusion).
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:7134; MLLT1 (Note=KMT2A-MLLT1 fusion).
CC   Genetic integration: Method=Transfection/transduction; Gene=UniProtKB; P00552; Klebsiella pneumoniae transposon Tn5 neo.
CC   Transformant: KMT2A-MLLT1.
CC   Omics: Transcriptomics; Microarray.
CC   Derived from site: In situ; Umbilical cord blood; UBERON=UBERON_0012168.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
AG   <1D
CA   Transformed cell line
DT   Created: 20-05-21; Last updated: 14-08-25; Version: 9
//
ID   PICALM6B
AC   CVCL_B3QW
DR   Wikidata; Q110433137
RX   PubMed=26075887;
CC   Knockout cell: Method=KO mouse; MGI; MGI:2385902; Picalm.
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:7132; KMT2A (Note=KMT2A-MLLT1 fusion).
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:7134; MLLT1 (Note=KMT2A-MLLT1 fusion).
CC   Transformant: KMT2A-MLLT1.
CC   Derived from site: In situ; Embryonic liver; UBERON=UBERON_0002107.
OX   NCBI_TaxID=10090; ! Mus musculus (Mouse)
SX   Sex unspecified
AG   14FD
CA   Transformed cell line
DT   Created: 16-12-21; Last updated: 19-12-24; Version: 6
//
ID   PICALM6D
AC   CVCL_B3QX
DR   Wikidata; Q110433138
RX   PubMed=26075887;
CC   Knockout cell: Method=KO mouse; MGI; MGI:2385902; Picalm.
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:7132; KMT2A (Note=KMT2A-MLLT1 fusion).
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:7134; MLLT1 (Note=KMT2A-MLLT1 fusion).
CC   Transformant: KMT2A-MLLT1.
CC   Derived from site: In situ; Embryonic liver; UBERON=UBERON_0002107.
OX   NCBI_TaxID=10090; ! Mus musculus (Mouse)
SX   Sex unspecified
AG   14FD
CA   Transformed cell line
DT   Created: 16-12-21; Last updated: 19-12-24; Version: 6
//
ID   PICALM6A
AC   CVCL_B3QV
DR   Wikidata; Q110433136
RX   PubMed=26075887;
CC   Knockout cell: Method=KO mouse; MGI; MGI:2385902; Picalm.
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:7132; KMT2A (Note=KMT2A-MLLT1 fusion).
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:7134; MLLT1 (Note=KMT2A-MLLT1 fusion).
CC   Transformant: KMT2A-MLLT1.
CC   Derived from site: In situ; Embryonic liver; UBERON=UBERON_0002107.
CC   Breed/subspecies: fit1 Picalmfit1-5R.
OX   NCBI_TaxID=10090; ! Mus musculus (Mouse)
SX   Sex unspecified
AG   14FD
CA   Transformed cell line
DT   Created: 16-12-21; Last updated: 19-12-24; Version: 6
//
ID   HB11;19
AC   CVCL_8227
SY   HB(11;19); HB11.19; HB 11;19; HB1119
DR   EFO; EFO_0022450
DR   cancercelllines; CVCL_8227
DR   Cell_Model_Passport; SIDM01428
DR   DepMap; ACH-001736
DR   Wikidata; Q54881357
RX   PubMed=1423624;
RX   PubMed=16523483;
CC   Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
CC   Sequence variation: Gene fusion; HGNC; HGNC:7132; KMT2A + HGNC; HGNC:7134; MLLT1; Name(s)=KMT2A-MLLT1, MLL-MLLT1, MLL-ENL (PubMed=1423624; PubMed=16523483; DepMap=ACH-001736).
CC   Sequence variation: Mutation; HGNC; HGNC:1787; CDKN2A; Simple; p.Arg80Ter (c.237_238CC>TT) (c.237_238delinsTT) (p.Pro94Leu, c.280_281CC>TT); Zygosity=Homozygous (DepMap=ACH-001736).
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Thr125Met (c.374C>T); ClinVar=VCV000183748; Zygosity=Unspecified (DepMap=ACH-001736).
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg248Trp (c.742C>T); ClinVar=VCV000012347; Zygosity=Unspecified (DepMap=ACH-001736).
CC   Omics: Genomics; Whole exome sequencing.
CC   Omics: Variations; Array-based CGH.
DI   NCIt; C80342; B acute lymphoblastic leukemia with t(v;11q23.3) MLL rearranged
DI   ORDO; Orphanet_585918; B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Age unspecified
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 14-08-25; Version: 22
//
ID   Kasumi-10
AC   CVCL_8485
SY   KASUMI-10
DR   GEO; GSM4254138
DR   GEO; GSM5137757
DR   JCRB; JCRB1410
DR   PRIDE; PXD023662
DR   Wikidata; Q54899515
RX   PubMed=32180206;
RX   PubMed=35354797;
CC   Population: Japanese and Korean.
CC   Karyotypic information: While originating from a female patient, it has a XXY karyotype that could be explained by a disorder of sexual development (PubMed=32180206).
CC   Sequence variation: Gene fusion; HGNC; HGNC:7132; KMT2A + HGNC; HGNC:7134; MLLT1; Name(s)=KMT2A-MLLT1, MLL-MLLT1, MLL-ENL (PubMed=32180206; PubMed=35354797).
CC   Sequence variation: Mutation; HGNC; HGNC:3765; FLT3; Unexplicit; Internal tandem duplication (FLT3-ITD); ClinVar=VCV000016270; Zygosity=Unspecified (PubMed=32180206).
CC   Omics: Proteomics; Quantitative.
CC   Omics: Transcriptomics; RNAseq.
CC   Omics: Variations; SNP array analysis.
CC   Miscellaneous: STR profile from personal communication of Leo, Isabelle Rose.
ST   Source(s): JCRB=JCRB1410; Direct_author_submission
ST   Amelogenin: X,Y
ST   CSF1PO: 11,12
ST   D10S1248: 12,15
ST   D12S391: 18,22
ST   D13S317: 8,11
ST   D16S539: 9,10
ST   D18S51: 13
ST   D19S433: 15.2,16
ST   D1S1656: 15,17
ST   D21S11: 30
ST   D22S1045: 15,17
ST   D2S1338: 19,24
ST   D2S441: 11,11.3
ST   D3S1358: 15,16
ST   D5S818: 10,12
ST   D7S820: 8,10
ST   D8S1179: 13,14
ST   DYS391: 9
ST   FGA: 22,27.2
ST   SE33: 20,26.2
ST   TH01: 6,9
ST   TPOX: 11,12
ST   vWA: 17,19
DI   NCIt; C9140; Childhood B acute lymphoblastic leukemia
DI   NCIt; C80342; B acute lymphoblastic leukemia with t(v;11q23.3) MLL rearranged
DI   ORDO; Orphanet_585918; B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   6M
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 10-04-25; Version: 22
//
ID   KOCL-51
AC   CVCL_6865
SY   KOCL51
DR   Cosmic; 1037749
DR   Cosmic; 2391173
DR   IARC_TP53; 28413
DR   Wikidata; Q54900283
RX   DOI=10.1016/B978-0-12-221970-2.50457-5;
RX   PubMed=1465024;
RX   PubMed=8180386;
RX   PubMed=9529133;
RX   PubMed=9738977;
RX   PubMed=10360377;
RX   PubMed=10995006;
RX   PubMed=14671638;
RX   PubMed=20519628;
RX   PubMed=20575032;
RX   PubMed=28569787;
RX   PubMed=29786757;
RX   PubMed=35124168;
CC   Population: Japanese.
CC   Sequence variation: Gene fusion; HGNC; HGNC:7132; KMT2A + HGNC; HGNC:7134; MLLT1; Name(s)=KMT2A-MLLT1, MLL-MLLT1, MLL-ENL (PubMed=28569787).
DI   NCIt; C9140; Childhood B acute lymphoblastic leukemia
DI   NCIt; C80342; B acute lymphoblastic leukemia with t(v;11q23.3) MLL rearranged
DI   ORDO; Orphanet_585918; B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   3M
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 19-12-24; Version: 22
//
ID   KOPN-1
AC   CVCL_3937
SY   Kopn-1; KOPN1
DR   BTO; BTO_0004944
DR   cancercelllines; CVCL_3937
DR   Cosmic; 996302
DR   Cosmic; 1037721
DR   Cosmic; 2391172
DR   IARC_TP53; 28407
DR   Wikidata; Q54900299
RX   DOI=10.1016/B978-0-12-221970-2.50457-5;
RX   PubMed=1465024;
RX   PubMed=8180386;
RX   PubMed=9738977;
RX   PubMed=10360377;
RX   PubMed=14504097;
RX   PubMed=14671638;
RX   PubMed=15843827;
RX   PubMed=20519628;
RX   PubMed=20575032;
RX   PubMed=28569787;
RX   PubMed=29786757;
RX   PubMed=31305009;
RX   PubMed=35124168;
CC   Population: Japanese.
CC   Sequence variation: Gene fusion; HGNC; HGNC:7132; KMT2A + HGNC; HGNC:7134; MLLT1; Name(s)=KMT2A-MLLT1, MLL-MLLT1, MLL-ENL (PubMed=14671638; PubMed=15843827).
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg248Gln (c.743G>A); ClinVar=VCV000012356; Zygosity=Unspecified (PubMed=20575032).
CC   Omics: Phenotyping; Drug screening.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C9140; Childhood B acute lymphoblastic leukemia
DI   NCIt; C80342; B acute lymphoblastic leukemia with t(v;11q23.3) MLL rearranged
DI   ORDO; Orphanet_585918; B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   9M
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 14-08-25; Version: 25
//
ID   KOCL-33
AC   CVCL_3991
SY   KOCL33; KOCL 33; Kocl-33
DR   BTO; BTO_0004937
DR   Cosmic; 996295
DR   Cosmic; 1037745
DR   Cosmic; 2391170
DR   IARC_TP53; 28409
DR   Wikidata; Q54900278
RX   DOI=10.1016/B978-0-12-221970-2.50457-5;
RX   PubMed=1465024;
RX   PubMed=8180386;
RX   PubMed=9529133;
RX   PubMed=9738977;
RX   PubMed=10360377;
RX   PubMed=10995006;
RX   PubMed=14504097;
RX   PubMed=14671638;
RX   PubMed=15843827;
RX   PubMed=20519628;
RX   PubMed=20575032;
RX   PubMed=28569787;
RX   PubMed=29786757;
RX   PubMed=31305009;
RX   PubMed=35124168;
CC   Population: Japanese.
CC   Sequence variation: Gene fusion; HGNC; HGNC:7132; KMT2A + HGNC; HGNC:7134; MLLT1; Name(s)=KMT2A-MLLT1, MLL-MLLT1, MLL-ENL (PubMed=14671638; PubMed=15843827).
CC   Omics: Phenotyping; Drug screening.
DI   NCIt; C9140; Childhood B acute lymphoblastic leukemia
DI   NCIt; C80342; B acute lymphoblastic leukemia with t(v;11q23.3) MLL rearranged
DI   ORDO; Orphanet_585918; B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   11M
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 14-08-25; Version: 25
//
ID   IMS-M1
AC   CVCL_A623
SY   IMS/M1; IMS/MI; IMS-MI
DR   Cosmic; 787437
DR   Cosmic; 975256
DR   Cosmic; 996321
DR   Cosmic; 1037672
DR   Cosmic; 1281319
DR   Cosmic; 2089654
DR   Cosmic; 2378128
DR   Wikidata; Q54897680
RX   DOI=10.1016/B978-0-12-221970-2.50457-5;
RX   PubMed=8180386;
RX   PubMed=8414510;
RX   PubMed=14504097;
RX   PubMed=14671638;
RX   PubMed=23955599;
CC   Population: Japanese.
CC   Characteristics: CSF2 dependent.
CC   Doubling time: 36-48 hours (DOI=10.1016/B978-0-12-221970-2.50457-5).
CC   Sequence variation: Gene fusion; HGNC; HGNC:7132; KMT2A + HGNC; HGNC:7136; MLLT3; Name(s)=KMT2A-MLLT3, MLL-MLLT3, MLL-AF9 (PubMed=14671638).
CC   Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
DI   NCIt; C9154; Adult acute myeloid leukemia
DI   ORDO; Orphanet_519; Acute myeloid leukemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   33Y
CA   Cancer cell line
DT   Created: 06-06-12; Last updated: 19-12-24; Version: 15
//
ID   KOPN-8
AC   CVCL_1866
SY   Kopn-8; KOPN8
DR   CLO; CLO_0037178
DR   EFO; EFO_0022428
DR   ArrayExpress; E-MTAB-2770
DR   ArrayExpress; E-MTAB-3610
DR   ArrayExpress; E-MTAB-7721
DR   ArrayExpress; E-MTAB-7722
DR   BioSample; SAMN03473535
DR   BioSample; SAMN10988515
DR   cancercelllines; CVCL_1866
DR   Cell_Model_Passport; SIDM01034
DR   ChEMBL-Cells; CHEMBL4295381
DR   ChEMBL-Targets; CHEMBL4296456
DR   Cosmic; 998710
DR   Cosmic; 999747
DR   Cosmic; 1037722
DR   Cosmic; 1130256
DR   Cosmic; 1191708
DR   Cosmic; 2491068
DR   Cosmic; 2542838
DR   Cosmic-CLP; 1330933
DR   DepMap; ACH-001106
DR   DSMZ; ACC-552
DR   DSMZCellDive; ACC-552
DR   EGA; EGAS00001000978
DR   GDSC; 1330933
DR   GEO; GSM887234
DR   GEO; GSM888308
DR   GEO; GSM1670000
DR   GEO; GSM5137722
DR   GEO; GSM5137766
DR   IARC_TP53; 28230
DR   LiGeA; CCLE_069
DR   LINCS_LDP; LCL-1088
DR   PharmacoDB; KOPN8_779_2019
DR   PRIDE; PXD023662
DR   PRIDE; PXD030304
DR   Progenetix; CVCL_1866
DR   PubChem_Cell_line; CVCL_1866
DR   Wikidata; Q54900325
RX   DOI=10.1016/B978-0-12-221970-2.50457-5;
RX   PubMed=2985879;
RX   PubMed=3159941;
RX   PubMed=3874327;
RX   PubMed=9067587;
RX   PubMed=9680106;
RX   PubMed=10233379;
RX   PubMed=14671638;
RX   PubMed=22460905;
RX   PubMed=26589293;
RX   PubMed=27397505;
RX   PubMed=28196595;
RX   PubMed=30285677;
RX   PubMed=30629668;
RX   PubMed=30894373;
RX   PubMed=31068700;
RX   PubMed=31160637;
RX   PubMed=35354797;
RX   PubMed=35839778;
WW   Info; MCLP; -; https://tcpaportal.org/mclp/
CC   Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
CC   Part of: COSMIC cell lines project.
CC   Part of: LL-100 blood cancer cell line panel.
CC   Part of: MD Anderson Cell Lines Project.
CC   Population: Japanese.
CC   Doubling time: ~48 hours (DSMZ=ACC-552).
CC   HLA typing: A*33:03,33:03; B*44:03,44:03; C*14:03,14:03 (PubMed=26589293).
CC   HLA typing: A*33:03:01,33:03:01; B*44:03:01,44:03:01; C*14:03,14:03; DPA1*01:03:01,02:02:02; DPB1*04:01:01,02:01:02; DQA1*01:02:01,01:02:01; DQB1*06:09:01,06:09:01; DRA*01:02:02,01:02:02; DRB1*13:02:01,13:02:01 (DSMZCellDive=ACC-552).
CC   Microsatellite instability: Stable (MSS) (Sanger).
CC   Sequence variation: Gene fusion; HGNC; HGNC:7132; KMT2A + HGNC; HGNC:7134; MLLT1; Name(s)=KMT2A-MLLT1, MLL-MLLT1, MLL-ENL (PubMed=31160637; PubMed=35354797; DSMZ=ACC-552).
CC   Sequence variation: Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000012582; Zygosity=Heterozygous (Cosmic-CLP=1330933; DepMap=ACH-001106).
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg248Gln (c.743G>A); ClinVar=VCV000012356; Zygosity=Heterozygous (Cosmic-CLP=1330933; DepMap=ACH-001106).
CC   Omics: Genomics; DNA methylation analysis.
CC   Omics: Genomics; Whole exome sequencing.
CC   Omics: Phenotyping; Drug screening.
CC   Omics: Proteomics; Expression; Reverse-phase protein array.
CC   Omics: Proteomics; Quantitative.
CC   Omics: Transcriptomics; Microarray.
CC   Omics: Transcriptomics; RNAseq.
CC   Omics: Variations; SNP array analysis.
CC   Genome ancestry: African=3.7%; Native American=0%; East Asian, North=80.77%; East Asian, South=13.03%; South Asian=0%; European, North=0%; European, South=2.49% (PubMed=30894373).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
ST   Source(s): Cosmic-CLP=1330933; DSMZ=ACC-552
ST   Amelogenin: X
ST   CSF1PO: 10,12
ST   D13S317: 8,11
ST   D16S539: 9,11
ST   D18S51: 14,22
ST   D19S433: 13,14
ST   D21S11: 29
ST   D2S1338: 20,23
ST   D3S1358: 15,16
ST   D5S818: 9,11
ST   D7S820: 8,10
ST   D8S1179: 13,16
ST   FGA: 18,21
ST   Penta D: 12,13
ST   Penta E: 12,20
ST   TH01: 6,10
ST   TPOX: 8,11
ST   vWA: 16,18
DI   NCIt; C9140; Childhood B acute lymphoblastic leukemia
DI   NCIt; C80342; B acute lymphoblastic leukemia with t(v;11q23.3) MLL rearranged
DI   ORDO; Orphanet_585918; B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   3M
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 10-04-25; Version: 39
//
RX   PubMed=26075887; DOI=10.1371/journal.pone.0129776; PMCID=PMC4467867;
RA   Mercer, Jacob L.
RA   Argus, Joseph P.
RA   Crabtree, Donna Marlana
RA   Keenan, Melissa M.
RA   Wilks, Moses Q.
RA   Chi, Jen-Tsan Ashley
RA   Bensinger, Steven J.
RA   Lavau, Catherine P.
RA   Wechsler, Daniel S.
RT   "Modulation of PICALM levels perturbs cellular cholesterol
RT   homeostasis.";
RL   PLoS ONE 10:e0129776.1-e0129776.20(2015).
//
RX   PubMed=9680106; DOI=10.1016/S0145-2126(98)00050-2;
RA   Matsuo, Yoshinobu
RA   Drexler, Hans Gunther
RT   "Establishment and characterization of human B cell precursor-leukemia
RT   cell lines.";
RL   Leuk. Res. 22:567-579(1998).
//
RX   PubMed=14504097; DOI=10.1182/blood-2003-02-0418;
RA   Taketani, Takeshi
RA   Taki, Tomohiko
RA   Sugita, Kanji
RA   Furuichi, Yoshiyuki
RA   Ishii, Eiichi
RA   Hanada, Ryoji
RA   Tsuchida, Masahiro
RA   Sugita, Kenichi
RA   Ida, Kohmei
RA   Hayashi, Yasuhide
RT   "FLT3 mutations in the activation loop of tyrosine kinase domain are
RT   frequently found in infant ALL with MLL rearrangements and pediatric
RT   ALL with hyperdiploidy.";
RL   Blood 103:1085-1088(2004).
//
RX   PubMed=35839778; DOI=10.1016/j.ccell.2022.06.010; PMCID=PMC9387775;
RA   Goncalves, Emanuel
RA   Poulos, Rebecca C.
RA   Cai, Zhao-Xiang
RA   Barthorpe, Syd
RA   Manda, Srikanth S.
RA   Lucas, Natasha
RA   Beck, Alexandra
RA   Bucio-Noble, Daniel
RA   Dausmann, Michael
RA   Hall, Caitlin
RA   Hecker, Michael
RA   Koh, Jennifer
RA   Lightfoot, Howard
RA   Mahboob, Sadia
RA   Mali, Iman
RA   Morris, James
RA   Richardson, Laura
RA   Seneviratne, Akila J.
RA   Shepherd, Rebecca
RA   Sykes, Erin
RA   Thomas, Frances
RA   Valentini, Sara
RA   Williams, Steven G.
RA   Wu, Yang-Xiu
RA   Xavier, Dylan
RA   MacKenzie, Karen L.
RA   Hains, Peter G.
RA   Tully, Brett
RA   Robinson, Phillip James
RA   Zhong, Qing
RA   Garnett, Mathew J.
RA   Reddel, Roger Robert
RT   "Pan-cancer proteomic map of 949 human cell lines.";
RL   Cancer Cell 40:835-849.e8(2022).
//
RX   PubMed=28196595; DOI=10.1016/j.ccell.2017.01.005; PMCID=PMC5501076;
RA   Li, Jun
RA   Zhao, Wei
RA   Akbani, Rehan
RA   Liu, Wen-Bin
RA   Ju, Zhen-Lin
RA   Ling, Shi-Yun
RA   Vellano, Christopher P.
RA   Roebuck, Paul
RA   Yu, Qing-Hua
RA   Eterovic, Agda Karina
RA   Byers, Lauren Averett
RA   Davies, Michael A.
RA   Deng, Wan-Leng
RA   Gopal, Y.N. Vashisht
RA   Chen, Guo
RA   von Euw, Erika Maria
RA   Slamon, Dennis Joseph
RA   Conklin, Dylan
RA   Heymach, John Victor
RA   Gazdar, Adi F.
RA   Minna, John D.
RA   Myers, Jeffrey N.
RA   Lu, Yi-Ling
RA   Mills, Gordon B.
RA   Liang, Han
RT   "Characterization of human cancer cell lines by reverse-phase protein
RT   arrays.";
RL   Cancer Cell 31:225-239(2017).
//
RX   PubMed=8180386; DOI=10.1182/blood.V83.10.2912.2912;
RA   Yamamoto, Kazuhito
RA   Seto, Masao
RA   Iida, Shinsuke
RA   Komatsu, Hirokazu
RA   Kamada, Nanao
RA   Kojima, Seiji
RA   Kodera, Yoshihisa
RA   Nakazawa, Shinpei
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RX   PubMed=30285677; DOI=10.1186/s12885-018-4840-5; PMCID=PMC6167786;
RA   Tan, Kar-Tong
RA   Ding, Ling-Wen
RA   Sun, Qiao-Yang
RA   Lao, Zhen-Tang
RA   Chien, Wenwen
RA   Ren, Xi
RA   Xiao, Jin-Fen
RA   Loh, Xin-Yi
RA   Xu, Liang
RA   Lill, Michael
RA   Mayakonda, Anand
RA   Lin, De-Chen
RA   Yang, Henry He
RA   Koeffler, Harold Phillip
RT   "Profiling the B/T cell receptor repertoire of lymphocyte derived cell
RT   lines.";
RL   BMC Cancer 18:940.1-940.13(2018).
//