CELL SEARCH SYSTEM

Cell Search
Keyword(s):
Enter one or more search terms.
  
Update information

Disease-specific iPS cells

*When you want to use some Disease-specific iPS cells, please e-mail to the following address.
*In relation to the information that are not described below, please e-mail to the following address.

Contact us : cellips.brcriken.jp

Blue letter cells are available. You obtain the information by clicking the blue letter.
*iPS cells created using the Sendai virus vector are now available

Update : 2015.12.01

Name of diseases Patient Cell line
1 Parkinson’s disease 7 14
2 Retinitis pigmentosa 7 11
3 Spinocerebellar Degeneration 4 10
4 X-Linked α-Thalassemia, Mental Retardation Syndrome (ATR-X syndrome) 1 2
5 Congenital Cerebral Hypomyelination 2 6
6 Moyamoya disease 2 6
7 Bardet-Biedl syndrome   1 3
8 Lysosomal storage disease    3 9
9 Huntington’s disease    1 1
10 Amyotrophic lateral sclerosis (ALS)   18 38
11 Spinal-Bulbar Muscular Atrophy    3 7
12 Spinal muscular atrophy    4 10
13 Primary lateral sclerosis (PLS)    2 5
14 Charcot-Marie-Tooth disease  5 11
15 Progressive systemic sclerosis (PSS)    2 6
16 Cockayne’s syndrome    1 3
17 Cryopirin-associated periodic syndrome 2 4
18 Osteogenesis Imperfecta    1 4
19 Hypophosphatasia    2 2
20 Achondroplasia    2 6
21 Fibrodysplasia ossificans progressiva (FOP)    2 3
22 Muscular dystrophy   12 43
23 Dermatomyositis (DM)    1 3
24 Inclusion body myositis   2 6
25 Congenital myopathy    1 3
26 Long QT Syndrome and Brugada Syndrome   1 2
27 Cardiomyopathy, dilated cardiomyopathy    2 3
28 Cardiomyopathy, hypertrophic cardiomyopathy (HCM)    3 NEW 6 NEW
29 Pulmonary hypertension    1 3
30 Primary Immunodeficiency:PID    3 11
31 Fanconi anemia    2 2
32 Severe congenital neutropenia    1 3
33 Epstein syndrome 1 3
34 Juvenile nephronophthisis    2 6
35 Sjögren’s syndrome    1 3
36 Ehlers-Danlos syndrome,   3 3
37 Nakajo-Nishimura Syndrome    2 2
38 Amyloid neuropathy    2 5
39 Glycogen storage disease    1 3
40 Glycogen storage disease    1 2
41 Werner syndrome    1 6
42 Wilson’s disease   3 12
43 Prader-Willi Syndrome   1 3
44 Ornithine transcarbamylase deficiency   1 3
45 Congenital disorders of biotin metabolism  1 3
46 Mitochondrial encephalomyopathy   3 9
47 Alzheimer disease  11 13
48 Dementia of Alzheimer’s type  1 1
49 Frontotemporal dementia  1 3
50 Familial central diabetes insipidus   1 1
51 Reticular dysgenesis 2 2
52 Rheumatoid Arthritis   2 6
53 Chédiak-Higashi syndrome  2 2
54 Kostmann syndrome   1 3
55 Bernard-Soulier syndorome   2 4
56 Pyruvate dehydrogenase deficiency   1 3
57 Atopic dermatitis   1 3
58 Allergic rhinitis (Pollen allergy)   1 1
59 Cancer 1 1
151 352