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3,883 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
HPS1651
 
Resource Report
Resource Website
RCB Cat# HPS1651, RRID:CVCL_C9RR Homo sapiens (Human) Ehlers-Danlos syndrome, type IV Induced pluripotent stem cell Male RCB HPS1651 RCB:HPS1651,
Wikidata:Q123031906
CVCL_C9RR 2026-09-19 06:13:54 0
HPS2027
 
Resource Report
Resource Website
RCB Cat# HPS2027, RRID:CVCL_C9V7 Homo sapiens (Human) AL amyloidosis Induced pluripotent stem cell Male RCB HPS2027 RCB:HPS2027,
Wikidata:Q123032018
CVCL_C9V7 2026-09-19 06:13:56 0
HPS2029
 
Resource Report
Resource Website
RCB Cat# HPS2029, RRID:CVCL_C9V9 Homo sapiens (Human) AL amyloidosis Induced pluripotent stem cell Male RCB HPS2029 RCB:HPS2029,
Wikidata:Q123032020
CVCL_C9V9 2026-09-19 06:13:56 0
HPS2091
 
Resource Report
Resource Website
RCB Cat# HPS2091, RRID:CVCL_D1CY Homo sapiens (Human) Sarcoidosis Induced pluripotent stem cell Male RCB HPS2091 RCB:HPS2091,
Wikidata:Q123032034
CVCL_D1CY 2026-09-19 06:13:56 0
HPS1996
 
Resource Report
Resource Website
RCB Cat# HPS1996, RRID:CVCL_C9QX Homo sapiens (Human) Autoimmune hemolytic anemia Induced pluripotent stem cell Female RCB HPS1996 RCB:HPS1996,
Wikidata:Q123031999
CVCL_C9QX 2026-09-19 06:13:56 0
HPS1995
 
Resource Report
Resource Website
RCB Cat# HPS1995, RRID:CVCL_C9QW Homo sapiens (Human) Autoimmune hemolytic anemia Induced pluripotent stem cell Female RCB HPS1995 RCB:HPS1995,
Wikidata:Q123031998
CVCL_C9QW 2026-09-19 06:13:56 0
HPS1994
 
Resource Report
Resource Website
RCB Cat# HPS1994, RRID:CVCL_C9QV Homo sapiens (Human) Autoimmune hemolytic anemia Induced pluripotent stem cell Female RCB HPS1994 RCB:HPS1994,
Wikidata:Q123031997
CVCL_C9QV 2026-09-19 06:13:56 0
HPS2053
 
Resource Report
Resource Website
RCB Cat# HPS2053, RRID:CVCL_C9VL Homo sapiens (Human) Seizure disorder Donor information: Patient suffering from hemiconvulsion-hemiplegia-epilepsy syndrome, unknown genetic etiology. Induced pluripotent stem cell Male RCB HPS2053 RCB:HPS2053,
Wikidata:Q123032032
CVCL_C9VL 2026-09-19 06:13:56 0
HPS1689
 
Resource Report
Resource Website
RCB Cat# HPS1689, RRID:CVCL_C9SN Homo sapiens (Human) Cri du chat syndrome Induced pluripotent stem cell Female RCB HPS1689 RCB:HPS1689,
Wikidata:Q123031940
CVCL_C9SN 2026-09-19 06:13:55 0
HPS2050
 
Resource Report
Resource Website
RCB Cat# HPS2050, RRID:CVCL_C9VI Homo sapiens (Human) Seizure disorder Donor information: Patient suffering from hemiconvulsion-hemiplegia-epilepsy syndrome, unknown genetic etiology. Induced pluripotent stem cell Male RCB HPS2050 RCB:HPS2050,
Wikidata:Q123032029
CVCL_C9VI 2026-09-19 06:13:56 0
HPS1688
 
Resource Report
Resource Website
RCB Cat# HPS1688, RRID:CVCL_C9SM Homo sapiens (Human) Cri du chat syndrome Induced pluripotent stem cell Female RCB HPS1688 RCB:HPS1688,
Wikidata:Q123031939
CVCL_C9SM 2026-09-19 06:13:55 0
HPS2052
 
Resource Report
Resource Website
RCB Cat# HPS2052, RRID:CVCL_C9VK Homo sapiens (Human) Seizure disorder Donor information: Patient suffering from hemiconvulsion-hemiplegia-epilepsy syndrome, unknown genetic etiology. Induced pluripotent stem cell Male RCB HPS2052 RCB:HPS2052,
Wikidata:Q123032031
CVCL_C9VK 2026-09-19 06:13:56 0
HPS2092
 
Resource Report
Resource Website
RCB Cat# HPS2092, RRID:CVCL_D1CZ Homo sapiens (Human) Sarcoidosis Induced pluripotent stem cell Male RCB HPS2092 RCB:HPS2092,
Wikidata:Q123032035
CVCL_D1CZ 2026-09-19 06:13:56 0
HPS1685
 
Resource Report
Resource Website
RCB Cat# HPS1685, RRID:CVCL_C9SJ Homo sapiens (Human) Cri du chat syndrome Induced pluripotent stem cell Female RCB HPS1685 RCB:HPS1685,
Wikidata:Q123031936
CVCL_C9SJ 2026-09-19 06:13:55 0
HPS2007
 
Resource Report
Resource Website
RCB Cat# HPS2007, RRID:CVCL_C9R2 Homo sapiens (Human) Ichthyosis Induced pluripotent stem cell Female RCB HPS2007 RCB:HPS2007,
Wikidata:Q123032004
CVCL_C9R2 2026-09-19 06:13:56 0
HPS1663
 
Resource Report
Resource Website
RCB Cat# HPS1663, RRID:CVCL_C9S3 Homo sapiens (Human) Sturge-Weber syndrome Induced pluripotent stem cell Male RCB HPS1663 RCB:HPS1663,
Wikidata:Q123031919
CVCL_C9S3 2026-09-19 06:13:55 0
HPS1670
 
Resource Report
Resource Website
RCB Cat# HPS1670, RRID:CVCL_C9SA Homo sapiens (Human) Moyamoya disease Induced pluripotent stem cell Female RCB HPS1670 RCB:HPS1670,
Wikidata:Q123031927
CVCL_C9SA 2026-09-19 06:13:55 0
HPS2018
 
Resource Report
Resource Website
RCB Cat# HPS2018, RRID:CVCL_C9R7 Homo sapiens (Human) Familial amyloidosis Induced pluripotent stem cell Male RCB HPS2018 RCB:HPS2018,
Wikidata:Q123032009
CVCL_C9R7 2026-09-19 06:13:56 0
HPS1672
 
Resource Report
Resource Website
RCB Cat# HPS1672, RRID:CVCL_C9SC Homo sapiens (Human) Moyamoya disease Induced pluripotent stem cell Female RCB HPS1672 RCB:HPS1672,
Wikidata:Q123031929
CVCL_C9SC 2026-09-19 06:13:55 0
HPS2019
 
Resource Report
Resource Website
RCB Cat# HPS2019, RRID:CVCL_C9R8 Homo sapiens (Human) Familial amyloidosis Induced pluripotent stem cell Male RCB HPS2019 RCB:HPS2019,
Wikidata:Q123032010
CVCL_C9R8 2026-09-19 06:13:56 0

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