Ghent University Academic Bibliography

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Paternal age at birth is an important determinant of offspring telomere length

Tim De Meyer (UGent) , Ernst Rietzschel (UGent) , Marc De Buyzere (UGent) , Dirk De Bacquer (UGent) , Wim Van Criekinge (UGent) , Gui De Backer (UGent) , Thierry Gillebert (UGent) , Patric Van Oostveldt (UGent) and Sofie Bekaert (UGent)

(2007) HUMAN MOLECULAR GENETICS. 16(24). p.3097-3102
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Association between variations in CAT and noise-induced hearing loss in two independent noise-exposed populations

A Konings, Lut Van Laer (UGent) , M Pawelczyk, PI Carlsson, ML Bondeson, E Rajkowska, A Dudarewicz, A Vandevelde, E Fransen, J Huyghe, et al.

(2007) HUMAN MOLECULAR GENETICS. 16(15). p.1872-1883
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The coding polymorphism T263I in TGF-beta 1 is associated with otosclerosis in two independent populations

M THYS, I SCHRAUWEN, K VANDERSTRAETEN, K JANSSENS, N DIELTJENS, K VAN DEN BOGAERT, E FRANSEN, W CHEN, M EALY, M CLAUSTRES, et al.

(2007) HUMAN MOLECULAR GENETICS. 16(17). p.2021-2030
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Molecular pathogenesis of multiple gastrointestinal stromal tumors in NF1 patients

Ophélia Maertens (UGent) , H PRENEN, A WOZNIAK, R SCIOT, Patrick Pauwels (UGent) , I DE WEVER, JR VERMEESCH, T DE RAEDT, Anne De Paepe (UGent) , Franki Speleman (UGent) , et al.

(2006) HUMAN MOLECULAR GENETICS. 15(6). p.1015-1023
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MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene

CT STORLAZZI, T FIORETOS, C SURACE, A LONOCE, A MASTRORILLI, B STROMBECK, P D'ADDABBO, F IACOVELLI, C MINERVINI, A AVENTIN, et al.

(2006) HUMAN MOLECULAR GENETICS. 15(6). p.933-942
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Fibulin-5 mutations: mechanisms of impaired elastic fiber formation in recessive cutis laxa

QR HU, Bart Loeys (UGent) , Paul Coucke (UGent) , Anne De Paepe (UGent) , RP MECHAM, J CHOI, EC DAVIS and Z URBAN

(2006) HUMAN MOLECULAR GENETICS. 15(23). p.3379-3386
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Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

Marc Cruts, Rosa Rademakers, Ilse Gijselinck, Julie van der Zee, Bart Dermaut (UGent) , Tim de Pooter, Peter de Rijk, Jurgen Del-Favero and Christine van Broeckhoven

(2005) HUMAN MOLECULAR GENETICS. 14(13). p.1753-1762
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Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease

K TANIGUCHI, K KOBAYASHI, K SAITO, H YAMANOUCHI, A OHNUMA, YK HAYASHI, H MANYA, DK JIN, M LEE, E PARANO, et al.

(2003) HUMAN MOLECULAR GENETICS. 12(5). p.527-534
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Identification of CDH1 germline missense mutations associated with functional inactivation of the E-cadherin protein in young gastric cancer probands

G SURIANO, C OLIVEIRA, P FERREIRA, JC MACHADO, MC BORDIN, Olivier De Wever (UGent) , Erik Bruyneel, N MOGUILEVSKY, N GREHAN, TR PORTER, et al.

(2003) HUMAN MOLECULAR GENETICS. 12(5). p.575-582
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E-cadherin germline missense mutations and cell phenotype: evidence for the independence of cell invasion on the motile capabilities of the cells

G SURIANO, MJ OLIVEIRA, D HUNTSMAN, AR MATEUS, P FERREIRA, F CASARES, C OLIVEIRA, F CARNEIRO, JC MACHADO, Marcus Mareel (UGent) , et al.

(2003) HUMAN MOLECULAR GENETICS. 12(22). p.3007-3016

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Academic Bibliography

Paternal age at birth is an important determinant of offspring telomere length

Association between variations in CAT and noise-induced hearing loss in two independent noise-exposed populations

The coding polymorphism T263I in TGF-beta 1 is associated with otosclerosis in two independent populations

Molecular pathogenesis of multiple gastrointestinal stromal tumors in NF1 patients

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene

Fibulin-5 mutations: mechanisms of impaired elastic fiber formation in recessive cutis laxa

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease

Identification of CDH1 germline missense mutations associated with functional inactivation of the E-cadherin protein in young gastric cancer probands

E-cadherin germline missense mutations and cell phenotype: evidence for the independence of cell invasion on the motile capabilities of the cells

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