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95,747 Results - per page

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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
CS267BE LCL
 
Resource Report
Resource Website
Coriell Cat# GM11550, RRID:CVCL_EG46 Homo sapiens (Human) Cockayne syndrome type B Population: Caucasian. Transformed cell line Female Cockayne Syndrome 267 BEthesda LCL, GM11550 Coriell GM11550 CLO:CLO_0021058,
Coriell:GM11550,
Wikidata:Q54845151
CVCL_EG46 2026-07-25 04:24:38 0
CS1YOM
 
Resource Report
Resource Website
RRID:CVCL_B5LU Homo sapiens (Human) Population: Japanese. PMID:6481688 Finite cell line Female Cockayne Syndrome 1 YOkohama Mother JCRB:KURB1958,
Wikidata:Q111733140
CVCL_B5LU 2026-07-25 04:24:37 0
cs-17-25
 
Resource Report
Resource Website
Discontinued
JCRB Cat# JCRB1102, RRID:CVCL_8546 Cricetulus griseus (Chinese hamster) Characteristics: Cold-sensitive mutant of CHL. Unable to form colonies in soft agar at 34.5 Celsius. PMID:1170023
PMID:2437133
PMID:8168155
Transformed cell line Female JCRB JCRB1102 JCRB:JCRB1102,
JCRB:NIHS0384,
Wikidata:Q54814520
cvcl_8483 CVCL_8546 2026-07-25 04:24:36 0
CS3GO
 
Resource Report
Resource Website
RRID:CVCL_ZT15 Homo sapiens (Human) Cockayne syndrome type B Caution: CS2GO (Cellosaurus=CVCL_ZT14) and CS3GO (Cellosaurus=CVCL_ZT15) originate from 2 siblings, however their mutation profile is different, different hypothesis are proposed about this issue (DOI=10.21954/ou.ro.0000e27e)., Population: Caucasian. Finite cell line Female Cockayne Syndrome 3 GOthenburg Wikidata:Q98125752 CVCL_ZT15 2026-07-25 04:24:38 0
CSES23
 
Resource Report
Resource Website
RRID:CVCL_B834 Homo sapiens (Human) From: Cedars-Sinai Medical Center; Los Angeles; USA. PMID:20641042 Embryonic stem cell Female Cedars Sinai Embryonic Stem cell 23 NIHhESC:NIHhESC-11-0120,
Wikidata:Q54814602
CVCL_B834 2026-07-25 04:24:39 0
CS6MO
 
Resource Report
Resource Website
RRID:CVCL_ZS06 Homo sapiens (Human) Cockayne syndrome PMID:431551 Finite cell line Female Cockayne Syndrome 6 MOntreal Wikidata:Q98125768 CVCL_ZS06 2026-07-25 04:24:38 0
CS7SE
 
Resource Report
Resource Website
RRID:CVCL_L469 Homo sapiens (Human) Cockayne syndrome type B Population: African American. PMID:157803
PMID:431551
PMID:7301938
PMID:7360141
PMID:7471106
PMID:12665480
PMID:27543334
Finite cell line Female Cockayne Syndrome 7 SEattle, CSRDSE, 74.47, 7447, GM01428, GM-1428, GM 1428, GM1428 CLO:CLO_0030774,
BioSample:SAMN00803882,
Coriell:GM01428,
JCRB:KURB1917,
Wikidata:Q54836824
CVCL_L469 2026-07-25 04:24:38 0
CS84iSMA-n12B
 
Resource Report
Resource Website
RRID:CVCL_A9T6 Homo sapiens (Human) Werdnig-Hoffmann disease Population: Caucasian., From: Cedars-Sinai Medical Center iPSC Core Facility; Los Angeles; USA. Induced pluripotent stem cell Female CS84iSMA-nxx Wikidata:Q102113723 cvcl_w564 CVCL_A9T6 2026-07-25 04:24:39 0
CS4BR
 
Resource Report
Resource Website
RRID:CVCL_W050 Homo sapiens (Human) Cockayne syndrome type B Population: Caucasian. PMID:8823375
PMID:8834235
PMID:9443879
Finite cell line Female Cockayne Syndrome 4 BRighton Wikidata:Q54814550 CVCL_W050 2026-07-25 04:24:38 0
CSES11
 
Resource Report
Resource Website
RRID:CVCL_B822 Homo sapiens (Human) From: Cedars-Sinai Medical Center; Los Angeles; USA. PMID:20224970 Embryonic stem cell Female Cedars Sinai Embryonic Stem cell 11 NIHhESC:NIHhESC-11-0110,
Wikidata:Q54814573
CVCL_B822 2026-07-25 04:24:40 0
CS6BR
 
Resource Report
Resource Website
RRID:CVCL_ZN79 Homo sapiens (Human) Cockayne syndrome type A Population: Caucasian. PMID:7664335
PMID:7825573
PMID:8834235
Finite cell line Female Cockayne Syndrome 6 BRighton Wikidata:Q98125767 CVCL_ZN79 2026-07-25 04:24:38 0
CSB-iPSC clone 3
 
Resource Report
Resource Website
RRID:CVCL_L645 Homo sapiens (Human) De Sanctis-Cacchione syndrome Population: Mexican., From: University of California, San Diego; San Diego; USA. PMID:22661500 Induced pluripotent stem cell Female CSB-iPSC cl3 Wikidata:Q54814561 cvcl_f146 CVCL_L645 2026-07-25 04:24:38 0
CS697CTO
 
Resource Report
Resource Website
RRID:CVCL_ZS08 Homo sapiens (Human) Cockayne syndrome PMID:157803
PMID:7067035
PMID:7360141
Finite cell line Female Cockayne Syndrome 697 Canada TOronto Wikidata:Q98125763 CVCL_ZS08 2026-07-25 04:24:38 0
CSES21
 
Resource Report
Resource Website
RRID:CVCL_B832 Homo sapiens (Human) Down syndrome From: Cedars-Sinai Medical Center; Los Angeles; USA. PMID:20641042
PMID:26070610
Embryonic stem cell Female Cedars Sinai Embryonic Stem cell 21 GEO:GSM1576690,
NIHhESC:NIHhESC-11-0118,
Wikidata:Q54814584
CVCL_B832 2026-07-25 04:24:39 0
CSES2
 
Resource Report
Resource Website
RRID:CVCL_B813 Homo sapiens (Human) PMID:18450823
PMID:20224970
PMID:20641042
PMID:23045682
PMID:28445466
Embryonic stem cell Female CSES02, Cedars Sinai Embryonic Stem cell 2 NIHhESC:NIHhESC-11-0106,
Wikidata:Q54814582
CVCL_B813 2026-07-25 04:24:40 0
CSEC [Human]
 
Resource Report
Resource Website
RRID:CVCL_E309 Homo sapiens (Human) Esophageal squamous cell carcinoma Population: Chinese. PMID:18477252 Cancer cell line Female Wikidata:Q54814570 CVCL_E309 2026-07-25 04:24:38 0
CSES17
 
Resource Report
Resource Website
RRID:CVCL_B828 Homo sapiens (Human) From: Cedars-Sinai Medical Center; Los Angeles; USA. Embryonic stem cell Female Cedars Sinai Embryonic Stem cell 17 NIHhESC:NIHhESC-11-0115,
Wikidata:Q54814579
CVCL_B828 2026-07-25 04:24:40 0
CS2GO
 
Resource Report
Resource Website
RRID:CVCL_ZT14 Homo sapiens (Human) Cockayne syndrome type B Caution: CS2GO (Cellosaurus=CVCL_ZT14) and CS3GO (Cellosaurus=CVCL_ZT15) originate from 2 siblings, however their mutation profile is different, different hypothesis are proposed about this issue (DOI=10.21954/ou.ro.0000e27e)., Population: Caucasian. PMID:8834235 Finite cell line Female Cockayne Syndrome 2 GOthenburg Wikidata:Q98125744 CVCL_ZT14 2026-07-25 04:24:37 0
CS4AN
 
Resource Report
Resource Website
RRID:CVCL_ZS05 Homo sapiens (Human) Cockayne syndrome PMID:431551 Finite cell line Female Cockayne Syndrome 4 ANn Arbor, UM111 Wikidata:Q98125757 CVCL_ZS05 2026-07-25 04:24:37 0
CS4BR LCL
 
Resource Report
Resource Website
RRID:CVCL_2557 Homo sapiens (Human) Cockayne syndrome type B Population: Caucasian. Transformed cell line Female Cockayne Syndrome 4 BRighton LCL, LB242, 242 ECACC:98062324,
Wikidata:Q54902050
CVCL_2557 2026-07-25 04:24:37 0

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