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(Q54947691)
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English
XP11BE
cell line
Xeroderma Pigmentosum 11 BEthesda
CS4BE
XP-CS-1
Po Co
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Statements
instance of
cell line
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
finite cell line
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
autologous cell line
XP11BE LCL
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
described by source
Repair of ultraviolet light damage in a variety of human fibroblast cell strains
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
Transformation and immortalization of diploid xeroderma pigmentosum fibroblasts
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
A xeroderma pigmentosum patient having a high residual activity of unscheduled DNA synthesis after UV is assigned to complementation group A
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
Xeroderma pigmentosum D-HeLa hybrids with low and high ultraviolet sensitivity associated with normal and diminished DNA repair ability, respectively
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
Xeroderma pigmentosum. An inherited diseases with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
established from medical condition
xeroderma pigmentosum-Cockayne syndrome complex
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
derived from organism type
Homo sapiens
sex or gender
female
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
Identifiers
Cellosaurus ID
CVCL_U690
1 reference
stated in
Cellosaurus release 44
retrieved
31 January 2023
Cellosaurus ID
CVCL_U690
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