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GM07982
cell line
GM7982
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Statements
instance of
cell line
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
finite cell line
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
autologous cell line
GM07983
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
described by source
Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
Isogenic pairs of wild type and mutant induced pluripotent stem cell (iPSC) lines from Rett syndrome patients as in vitro disease model
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
Spectrum of MECP2 mutations in Rett syndrome
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
Loss of MECP2 Leads to Activation of P53 and Neuronal Senescence.
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
established from medical condition
Rett syndrome
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
derived from organism type
Homo sapiens
sex or gender
female
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
exact match
http://purl.obolibrary.org/obo/CLO_0010001
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
Identifiers
Cell Line Ontology ID
CLO_0010001
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
Cellosaurus ID
CVCL_V341
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_V341
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