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1 nd/or shortened lifespan (Werner, Bloom, and Rothmund-Thomson syndromes).
2 s, have been linked to the progeroid disease Rothmund-Thomson Syndrome.
3  human RecQL4 cause a rare genetic disorder, Rothmund-Thomson syndrome.
4 log (xRTS) of the RECQL4 helicase mutated in Rothmund-Thomson syndrome.
5  aging: Werner syndrome, Bloom syndrome, and Rothmund-Thomson syndrome.
6 osum, Cockayne syndrome, Bloom syndrome, and Rothmund-Thomson syndrome.
7 ition diseases, causing Bloom's, Werner, and Rothmund-Thomson syndromes.
8  trichothiodystrophy, ataxia-telangiectasia, Rothmund-Thomson syndrome, and xeroderma pigmentosum.
9 elicase diseases, such as Werner, Bloom, and Rothmund-Thomson syndromes, are also related to replicat
10 uld rescue UV sensitivity of RecQ4-deficient Rothmund-Thomson syndrome cells.
11 ncluding Werner Syndrome, Bloom Syndrome and Rothmund-Thomson Syndrome, exhibit genomic instability w
12                                          The Rothmund-Thomson syndrome (growth retardation, skin and
13  Deletion of the conserved C-terminus of the Rothmund-Thomson syndrome helicase RECQ4 is highly tumor
14 the pathogenesis of a subset of cancer-prone Rothmund-Thomson syndrome, is highly elevated in metasta
15 ient in the cancer-prone and premature aging Rothmund-Thomson syndrome, physically and functionally i
16                         RECQL4, deficient in Rothmund-Thomson Syndrome, promotes the two major DSB re
17 M mutation), Werner Syndrome (WRN mutation), Rothmund-Thomson Syndrome (RECQL4 mutation), and other g
18 d RECQL4 are mutated in Bloom's, Werner, and Rothmund Thomson syndromes, respectively.
19 sorders (Bloom syndrome, Werner syndrome and Rothmund-Thomson syndrome, respectively) that display in
20 genes are defective in Bloom's, Werner's and Rothmund-Thomson syndromes, respectively.
21                                Patients with Rothmund-Thomson syndrome (RTS) and RECQL4 gene mutation
22                                              Rothmund-Thomson syndrome (RTS) is a rare autosomal rece
23                                              Rothmund-Thomson syndrome (RTS) is an autosomal recessiv
24                                              Rothmund-Thomson syndrome (RTS) is an autosomal-recessiv
25 chinson-Gilford progeria syndrome (HGPS) and Rothmund-Thomson syndrome (RTS) patients compared with n
26 ave been identified in patients with Type II Rothmund-Thomson syndrome (RTS) with osteosarcoma predis
27 approximately two-thirds of individuals with Rothmund-Thomson syndrome (RTS), a disease characterized
28 Mutations in the DNA helicase RECQL4 lead to Rothmund-Thomson syndrome (RTS), a disorder characterize
29                   Mutations in RECQ4 lead to Rothmund-Thomson syndrome (RTS), and mouse models reveal
30  instability disorders, Bloom syndrome (BS), Rothmund-Thomson syndrome (RTS), and Werner syndrome (WS
31 n about RECQL4, the RecQ helicase mutated in Rothmund-Thomson syndrome (RTS).
32 ree of six families previously classified as Rothmund-Thomson syndrome (RTS-a poikiloderma that is so
33 the determinants of human Bloom, Werner, and Rothmund-Thomson syndromes, the shortened lifespan of to
34 mal recessive cancer-predisposition disorder Rothmund-Thomson syndrome, though it is unclear how thes
35                                      Type II Rothmund-Thomson syndrome (Type II RTS) is a rare autoso
36 and cause mitochondrial dysfunction, such as Rothmund-Thomson syndrome, Werner syndrome, and Cockayne
37 the RECQL4 helicase gene have been linked to Rothmund-Thomson syndrome, which is characterized by gen
38 have been linked to three diseases including Rothmund-Thomson syndrome, which is characterized by ost