Cancer Letters - Special Issue

FRAGILOME - COMMON FRAGILE SITES, GENOMIC INSTABILITY AND CANCER
edited by Manfred Schwab

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Article Title Author(s) Type Pages
Fragilome: Determining the role of fragile sites in human disease

28 January 2006 (Vol. 232 | No. 1 | Pages 1-3)

Manfred Schwab Editorial

1-3
Common fragile sites

28 January 2006 (Vol. 232 | No. 1 | Pages 4-12)

Thomas W. Glover Short survey

4-12
The molecular basis of common and rare fragile sites

28 January 2006 (Vol. 232 | No. 1 | Pages 13-26)

Michal Schwartz, Eitan Zlotorynski, Batsheva Kerem Short survey

13-26
Roles of FHIT and WWOX fragile genes in cancer

28 January 2006 (Vol. 232 | No. 1 | Pages 27-36)

Dimitrios Iliopoulos, Gulnur Guler, Shuang-Yin Han, Teresa Druck, Michelle Ottey, Kelly A. McCorkell, Kay Huebner et al. Short survey

27-36
Common chromosomal fragile sites and cancer: Focus on FRA16D

28 January 2006 (Vol. 232 | No. 1 | Pages 37-47)

Louise V. O'Keefe, Robert I. Richards Short survey

37-47
Common fragile sites, extremely large genes, neural development and cancer

28 January 2006 (Vol. 232 | No. 1 | Pages 48-57)

David I Smith, Yu Zhu, Sarah McAvoy, Robert Kuhn Short survey

48-57
Low-frequency common fragile sites: Link to neuropsychiatric disorders?

28 January 2006 (Vol. 232 | No. 1 | Pages 58-69)

Larissa Savelyeva, Evgeny Sagulenko, Jens Guido Schmitt, Manfred Schwab Short survey

58-69
Chromatin structure of human chromosomal fragile sites

28 January 2006 (Vol. 232 | No. 1 | Pages 70-78)

Yuh-Hwa Wang Short survey

70-78
Manifestation, mechanisms and mysteries of gene amplifications

28 January 2006 (Vol. 232 | No. 1 | Pages 79-89)

Samuel Myllykangas, Sakari Knuutila Short survey

79-89
Oncogenic rearrangements of the NTRK1/NGF receptor

28 January 2006 (Vol. 232 | No. 1 | Pages 90-98)

Marco A. Pierotti, Angela Greco Short survey

90-98
Disruption of the Fanconi anemia/BRCA pathway in sporadic cancer

28 January 2006 (Vol. 232 | No. 1 | Pages 99-106)

Alex Lyakhovich, Jordi Surralles Short survey

99-106
Rothmund–Thomson syndrome and RECQL4 defect: Splitting and lumping

28 January 2006 (Vol. 232 | No. 1 | Pages 107-120)

Lidia Larizza, Ivana Magnani, Gaia Roversi Short survey

107-120
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