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Thomas Glover
Thomas Glover
Unknown affiliation
Verified email at umich.edu
Title
Cited by
Cited by
Year
Mutations in the p53 gene occur in diverse human tumour types
JM Nigro, SJ Baker, AC Preisinger, JM Jessup, R Hosteller, K Cleary, ...
Nature 342 (6250), 705-708, 1989
36541989
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
M Eriksson, WT Brown, LB Gordon, MW Glynn, J Singer, L Scott, ...
Nature 423 (6937), 293-298, 2003
25672003
Chromosome fragile sites
SG Durkin, TW Glover
Annu. Rev. Genet. 41 (1), 169-192, 2007
8472007
Isolation of a partial candidate gene for Menkes disease by positional cloning
JFB Mercer, J Livingston, B Hall, JA Paynter, C Begy, ...
Nature genetics 3 (1), 20-25, 1993
8301993
Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patients
TN Basu, DH Gutmann, JA Fletcher, TW Glover, FS Collins, J Downward
Nature 356 (6371), 713-715, 1992
8211992
DNA polymerase α inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
TW Glover, C Berger, J Coyle, B Echo
Human genetics 67 (2), 136-142, 1984
7381984
ATR regulates fragile site stability
AM Casper, P Nghiem, MF Arlt, TW Glover
Cell 111 (6), 779-789, 2002
7022002
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome
J Fang, SL Dagenais, RP Erickson, MF Arlt, MW Glynn, JL Gorski, ...
The American Journal of Human Genetics 67 (6), 1382-1388, 2000
7022000
A de novo Alu insertion results in neurofibromatosis type 1
MR Wallace, LB Andersen, AM Saulino, PE Gregory, TW Glover, ...
Nature 353 (6347), 864-866, 1991
5731991
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis
E Legius, DA Marchuk, FS Collins, TW Glover
Nature genetics 3 (2), 122-126, 1993
4781993
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative RhoRac guanine nucleotide exchange factor
NG Pasteris, A Cadle, LJ Logie, MEM Porteous, CE Schwartz, ...
Cell 79 (4), 669-678, 1994
3841994
The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability
NG Howlett, T Taniguchi, SG Durkin, AD D'Andrea, TW Glover
Human molecular genetics 14 (5), 693-701, 2005
3362005
FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites
CM Wilke, BK Hall, A Hoge, W Paradee, DI Smith, TW Glover
Human molecular genetics 5 (2), 187-195, 1996
3091996
Incomplete processing of mutant lamin A in Hutchinson–Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition
MW Glynn, TW Glover
Human molecular genetics 14 (20), 2959-2969, 2005
2992005
Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction
MM Le Beau, FV Rassool, ME Neilly, R Espinosa III, TW Glover, DI Smith, ...
Human molecular genetics 7 (4), 755-761, 1998
2891998
FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition.
TW Glover
American Journal of Human Genetics 33 (2), 234, 1981
2771981
X‐linked mental retardation: A study of 7 families
PA Jacobs, TW Glover, M Mayer, P Fox, JW Gerrard, HG Dunn, DS Herbst, ...
American journal of medical genetics 7 (4), 471-489, 1980
2741980
Common fragile sites as targets for chromosome rearrangements
MF Arlt, SG Durkin, RL Ragland, TW Glover
DNA repair 5 (9-10), 1126-1135, 2006
2562006
Fragile sites in cancer: more than meets the eye
TW Glover, TE Wilson, MF Arlt
Nature Reviews Cancer 17 (8), 489-501, 2017
2452017
Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutant
J Lee, JR Prohaska, SL Dagenais, TW Glover, DJ Thiele
Gene 254 (1-2), 87-96, 2000
2402000
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