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(Q54609735)
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AG03258
cell line
AG3258
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Statements
instance of
cell line
1 reference
stated in
Cellosaurus release 49
retrieved
12 July 2024
Cellosaurus ID
CVCL_L622
finite cell line
1 reference
stated in
Cellosaurus release 49
retrieved
12 July 2024
Cellosaurus ID
CVCL_L622
described by source
Familial co-segregation of the elastin phenotype in skin fibroblasts from Hutchinson-Gilford progeria
1 reference
stated in
Cellosaurus release 49
retrieved
12 July 2024
Cellosaurus ID
CVCL_L622
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
1 reference
stated in
Cellosaurus release 49
retrieved
12 July 2024
Cellosaurus ID
CVCL_L622
Nucleolar expansion and elevated protein translation in premature aging
1 reference
stated in
Cellosaurus release 49
retrieved
12 July 2024
Cellosaurus ID
CVCL_L622
The National Institute on Aging repository cell cultures
1 reference
stated in
Cellosaurus release 49
retrieved
12 July 2024
Cellosaurus ID
CVCL_L622
derived from organism type
Homo sapiens
sex or gender
male
1 reference
stated in
Cellosaurus release 49
retrieved
12 July 2024
Cellosaurus ID
CVCL_L622
exact match
http://purl.obolibrary.org/obo/CLO_0036989
1 reference
stated in
Cellosaurus release 49
retrieved
12 July 2024
Cellosaurus ID
CVCL_L622
Identifiers
Cell Line Ontology ID
CLO_0036989
1 reference
stated in
Cellosaurus release 49
retrieved
12 July 2024
Cellosaurus ID
CVCL_L622
Cellosaurus ID
CVCL_L622
1 reference
stated in
Cellosaurus release 49
retrieved
12 July 2024
Cellosaurus ID
CVCL_L622
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