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csa (30) 30
cockayne syndrome (22) 22
index medicus (22) 22
humans (20) 20
cockayne syndrome - genetics (17) 17
dna repair (17) 17
dna damage (15) 15
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csb (14) 14
poly-adp-ribose binding proteins (12) 12
xeroderma-pigmentosum (12) 12
biochemistry & molecular biology (11) 11
dna helicases - genetics (11) 11
repair (11) 11
rna-polymerase-ii (11) 11
transcription factors - genetics (11) 11
dna repair enzymes - metabolism (10) 10
nucleotide excision-repair (10) 10
transcription (10) 10
genetics & heredity (9) 9
mutation (9) 9
dna-repair (8) 8
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cell biology (7) 7
cockayne-syndrome (7) 7
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dna helicases - metabolism (7) 7
multidisciplinary sciences (7) 7
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deoxyribonucleic acid--dna (5) 5
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Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1040 - 14
Journal Article
Human Mutation, ISSN 1059-7794, 02/2010, Volume 31, Issue 2, pp. 113 - 126
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2016, Volume 113, Issue 44, pp. 12502 - 12507
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2014, Volume 111, Issue 40, pp. 14454 - 14459
Journal Article
DNA Repair, ISSN 1568-7864, 11/2019, Volume 83, p. 102696
•Increased senescence in SH-SY5Y cells lacking CSA or CSB.•Developmental abnormalities in zebrafish lacking CSB following exposure to UV.•Release of crystallin... 
CSA | Transcription dysregulation | CSB | Neurodegeneration | Cockyane syndrome | UV-IRRADIATION | CSB/ERCC6 | RECRUITMENT | RNA | DNA-DAMAGE | TRANSCRIPTION | DEFECT | REPAIR | GENETICS & HEREDITY | TOXICOLOGY | AGGREGATION | CATARACT
Journal Article
Molecular Cell, ISSN 1097-2765, 2017, Volume 68, Issue 6, pp. 1054 - 1066.e6
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 13686 - 9
There are two genetics complementary groups Cockayne syndrome type A and B (CS-A and CS-B OMIM 216400, 133540), which is a rare autosomal recessive segmental... 
CSA | DIAGNOSIS | ERCC8 | PROTEIN | MUTATIONS | MULTIDISCIPLINARY SCIENCES | Cockayne syndrome | Complementation | Mutation
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2015, Volume 53, Issue 3, pp. 262 - 265
Journal Article
Journal Article