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  • References:pmid:23665875 (facet)

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1,669 Results - per page

Show More Columns | Download Top 1000 Results

Name Proper Citation Organism Disease Comments Defining Citation Category Sex Synonyms Vendor Catalog Number Cross References Hierarchy Originate from Same Individual ID Record Last Update Mentions Count
GM13540
 
Resource Report
Resource Website
Coriell Cat# GM13540, RRID:CVCL_5Q07 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM13540 CLO:CLO_0012440,
BioSample:SAMN00802460,
Coriell:GM13540,
Wikidata:Q54846624
CVCL_5Q07 2026-09-12 05:34:51 0
GM13555
 
Resource Report
Resource Website
Coriell Cat# GM13555, RRID:CVCL_U538 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM13555 CLO:CLO_0012476,
BioSample:SAMN00802474,
Coriell:GM13555,
Wikidata:Q54846633
CVCL_U538 2026-09-12 05:34:52 0
GM13553
 
Resource Report
Resource Website
Coriell Cat# GM13553, RRID:CVCL_U537 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell GM13553 CLO:CLO_0012479,
BioSample:SAMN00802470,
Coriell:GM13553,
Wikidata:Q54846631
CVCL_U537 2026-09-12 05:34:52 0
GM13540
 
Resource Report
Resource Website
RRID:CVCL_5Q07 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0012440,
BioSample:SAMN00802460,
Coriell:GM13540,
Wikidata:Q54846624
CVCL_5Q07 2026-09-12 05:34:51 0
GM13688
 
Resource Report
Resource Website
Coriell Cat# GM13688, RRID:CVCL_2U32 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM13688 CLO:CLO_0032752,
BioSample:SAMN00802534,
Coriell:GM13688,
Wikidata:Q54846717
CVCL_2U32 2026-09-12 05:34:54 0
GM13721
 
Resource Report
Resource Website
Coriell Cat# GM13721, RRID:CVCL_5Q10 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM13721 CLO:CLO_0032797,
BioSample:SAMN00802574,
Coriell:GM13721,
Wikidata:Q54846751
CVCL_5Q10 2026-09-12 05:34:54 0
GM13732
 
Resource Report
Resource Website
Coriell Cat# GM13732, RRID:CVCL_2U34 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM13732 CLO:CLO_0032761,
BioSample:SAMN00802578,
Coriell:GM13732,
Wikidata:Q54846753
CVCL_2U34 2026-09-12 05:34:54 0
GM13783
 
Resource Report
Resource Website
Possibly Discontinued
RRID:CVCL_V480 Homo sapiens (Human) Down syndrome PMID:23665875 Transformed cell line Female CLO:CLO_0033491,
BioSample:SAMN00802608,
Coriell:GM13783,
Wikidata:Q54846781
CVCL_V480 2026-09-12 05:34:55 0
GM13783
 
Resource Report
Resource Website
Possibly Discontinued
Coriell Cat# GM13783, RRID:CVCL_V480 Homo sapiens (Human) Down syndrome PMID:23665875 Transformed cell line Female Coriell GM13783 CLO:CLO_0033491,
BioSample:SAMN00802608,
Coriell:GM13783,
Wikidata:Q54846781
CVCL_V480 2026-09-12 05:34:55 0
GM13732
 
Resource Report
Resource Website
RRID:CVCL_2U34 Homo sapiens (Human) PMID:23665875 Transformed cell line Male CLO:CLO_0032761,
BioSample:SAMN00802578,
Coriell:GM13732,
Wikidata:Q54846753
CVCL_2U34 2026-09-12 05:34:54 0
GM13744
 
Resource Report
Resource Website
RRID:CVCL_2U38 Homo sapiens (Human) PMID:23665875 Transformed cell line Female CLO:CLO_0032776,
BioSample:SAMN00802590,
Coriell:GM13744,
Wikidata:Q54846771
CVCL_2U38 2026-09-12 05:34:54 0
GM13734
 
Resource Report
Resource Website
Coriell Cat# GM13734, RRID:CVCL_2U36 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM13734 CLO:CLO_0032764,
BioSample:SAMN00802582,
Coriell:GM13734,
Wikidata:Q54846767
CVCL_2U36 2026-09-12 05:34:54 0
GM50168
 
Resource Report
Resource Website
Coriell Cat# GM50168, RRID:CVCL_5L31 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL339 Coriell GM50168 CLO:CLO_0015018,
Coriell:GM50168,
Wikidata:Q54854241
CVCL_5L31 2026-09-12 05:37:48 0
GM50160
 
Resource Report
Resource Website
RRID:CVCL_5L28 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Female JL305 CLO:CLO_0014717,
Coriell:GM50160,
Wikidata:Q54854234
CVCL_5L28 2026-09-12 05:37:48 0
GM50124
 
Resource Report
Resource Website
Coriell Cat# GM50124, RRID:CVCL_1U16 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL208 Coriell GM50124 CLO:CLO_0014753,
Coriell:GM50124,
Wikidata:Q54854209
CVCL_1U16 2026-09-12 05:37:47 0
GM50159
 
Resource Report
Resource Website
RRID:CVCL_5T53 Homo sapiens (Human) PMID:23665875 Transformed cell line Female JL298 CLO:CLO_0014716,
Coriell:GM50159,
Wikidata:Q54854229
CVCL_5T53 2026-09-12 05:37:48 0
GM50121
 
Resource Report
Resource Website
RRID:CVCL_0G78 Homo sapiens (Human) Holoprosencephaly PMID:7485158
PMID:23665875
Transformed cell line Male JL182 CLO:CLO_0014751,
Coriell:GM50121,
Wikidata:Q54854207
CVCL_0G78 2026-09-12 05:37:47 0
GM50139
 
Resource Report
Resource Website
RRID:CVCL_0G55 Homo sapiens (Human) PMID:23665875 Transformed cell line Female JL259 CLO:CLO_0014675,
Coriell:GM50139,
Wikidata:Q54854216
CVCL_0G55 2026-09-12 05:37:47 0
GM50121
 
Resource Report
Resource Website
Coriell Cat# GM50121, RRID:CVCL_0G78 Homo sapiens (Human) Holoprosencephaly PMID:7485158
PMID:23665875
Transformed cell line Male JL182 Coriell GM50121 CLO:CLO_0014751,
Coriell:GM50121,
Wikidata:Q54854207
CVCL_0G78 2026-09-12 05:37:47 0
GM50165
 
Resource Report
Resource Website
RRID:CVCL_5L30 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL330 CLO:CLO_0015015,
Coriell:GM50165,
Wikidata:Q54854238
CVCL_5L30 2026-09-12 05:37:48 0

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