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Cell Model Catalogue
Patient-Derived Cell Lines
Genetically Modified Cell Lines
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Cell Type
- None -
iPSC
no sample
only primary culture
ICD
- None -
E34.8
E71.1
E71.520
E75.2
E85.9
F00.
F06.9
F84.0
G35.0
G40.3
G43.8
G71.0
G71.2
G71.3
G93.4
I42.0
I42.1
I42.2
I42.80
I47.2
I48.-
I49.8
I50.3
I51.81
I64
L93.2
Q02
Q04.8
Q21.3
Q23.4
Q78.2
Q87.0
Q87.1
Q87.4
Q87.8
R00.1
Unknown
WT
Disease
- None -
Alström syndrome
Alternating hemiplegia
Arrhythmogenic right ventricular cardiomyopathy
Atrial fibrillation
Autism
Barth syndrome
Bradycardia
Brugada syndrome
Cardiofaciocutaneous syndrome
Cardiomyopathy after chemotherapy
Catecholaminergic polymorphic ventricular tachycardia
Childhood autism
Dementia in Alzheimer disease
Dilated cardiomyopathy
Early infantile epileptic encephalopathy
Encephalopathy
Generalised epilepsy with febrile seizure plus
Heart Failure with Preserved Ejection Fraction
Hypertrophic cardiomyopathy
Hypertrophic obstructive cardiomyopathy
Hypoplastic left heart syndrome
Kabuki syndrome
Lipid storage disorder
Long QT syndrome 1
Long QT syndrome 2
Long QT syndrome 3
Long QT syndrome 7
Marfan syndrome
Mental disorder
Microcephaly
Mitochondrial myopathy
Multiple sclerosis
Muscular dystrophy
Neonatal lupus erythematosus
Noonan syndrome
Noonan syndrome with multiple lentigines
Osteopetrosis
Overlap syndrome
Periventricular nodular heterotopia
Peroxisome biogenesis disorder spectrum
Progeroid syndrome
Short QT syndrome
Stroke heart syndrome
Takotsubo syndrome
Tetralogy of Fallot
Transthyretin amyloidosis
Ventricular tachycardia
Vici syndrome
WT
WT/Relative
X-linked adrenoleukodystrophy
X-linked myotubular myopathy
Source
- None -
Blood
Bone Marrow
Fibroblasts
Gingiva
Hair
Myoblasts
Skin
Urine
Reprogramming
- None -
Lentivirus
Plasmid
Retrovirus
Sendai Virus
Unknown
mRNA
Distribution
- None -
Project
UMG Collection
Gender
- None -
Male
Female
Unknown
Age
- None -
0-10
10-19
20-29
30-39
40-49
50-59
60-69
70-79
<= 80
hPSCreg Name
Cell Type
ICD Code
Disease
Source
Reprogramming
Distribution
Show All
UMGi085-A
iPSC
WT
WT/Relative
Skin
Sendai Virus
Project
UMGi086-A
iPSC
WT
WT/Relative
Skin
Sendai Virus
Project
UMGi087-A
iPSC
G43.8
Alternating hemiplegia
Fibroblasts
Lentivirus
Project
UMGi088-A
iPSC
G43.8
Alternating hemiplegia
Fibroblasts
Lentivirus
Project
UMGi089-A
iPSC
Q87.8
Peroxisome biogenesis disorder spectrum
Fibroblasts
Sendai Virus
Project
UMGi090-A
iPSC
G35.0
Multiple sclerosis
Skin
Sendai Virus
Project
UMGi091-A
iPSC
G35.0
Multiple sclerosis
Skin
Sendai Virus
Project
UMGi092-A
iPSC
G40.3
Generalised epilepsy with febrile seizure plus
Skin
Sendai Virus
UMG Collection
UMGi093-A
iPSC
WT
WT/Relative
Skin
Sendai Virus
Project
UMGi094-A
iPSC
WT
WT/Relative
Skin
Sendai Virus
Project
UMGi095-A
iPSC
E34.8
Progeroid syndrome
Fibroblasts
Sendai Virus
Project
UMGi096-A
iPSC
F00.
Dementia in Alzheimer disease
Fibroblasts
Sendai Virus
Project
UMGi097-A
iPSC
E34.8
Progeroid syndrome
Fibroblasts
Sendai Virus
Project
UMGi098-A
iPSC
G71.3
Mitochondrial myopathy
Fibroblasts
Sendai Virus
Project
UMGi136-A
iPSC
G71.3
Mitochondrial myopathy
Fibroblasts
Sendai Virus
Project
UMGi099-A
iPSC
Q87.8
Alström syndrome
Skin
mRNA
UMG Collection
UMGi099-B
iPSC
Q87.8
Alström syndrome
Skin
Sendai Virus
UMG Collection
UMGi100-A
iPSC
Q87.1
Noonan syndrome with multiple lentigines
Fibroblasts
Sendai Virus
UMG Collection
UMGi134-A
iPSC
Q87.1
Cardiofaciocutaneous syndrome
Fibroblasts
Sendai Virus
UMG Collection
UMGi102-A
iPSC
Q87.1
Noonan syndrome
Blood
Sendai Virus
Project
Pagination
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