Volume 16; Issue 18

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Human Molecular Genetics
Volume 16; Issue 18

Human Molecular Genetics

Volume 16; Issue 18

1

Intrinsic mitochondrial dysfunction in ATM-deficient lymphoblastoid cells

Ambrose, M., Goldstine, J. V., Gatti, R. A.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 552 KB

english, 2007

2

Association of attentional network function with exon 5 variations of the CHRNA4 gene

Winterer, G., Musso, F., Konrad, A., Vucurevic, G., Stoeter, P., Sander, T., Gallinat, J.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 356 KB

english, 2007

3

Trans-generational epistasis between Dnd1Ter and other modifier genes controls susceptibility to testicular germ cell tumors

Lam, M.-Y. J., Heaney, J. D., Youngren, K. K., Kawasoe, J. H., Nadeau, J. H.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 140 KB

english, 2007

4

A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect

Simmonds, M. J., Howson, J. M.M., Heward, J. M., Carr-Smith, J., Franklyn, J. A., Todd, J. A., Gough, S. C.L.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 79 KB

english, 2007

5

Cholesterol biosynthesis pathway is disturbed in YAC128 mice and is modulated by huntingtin mutation

Valenza, M., Carroll, J. B., Leoni, V., Bertram, L. N., Bjorkhem, I., Singaraja, R. R., Di Donato, S., Lutjohann, D., Hayden, M. R., Cattaneo, E.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 567 KB

english, 2007

6

In vitro demonstration of intra-locus compensation using the ornithine transcarbamylase protein as model

Suriano, G., Azevedo, L., Novais, M., Boscolo, B., Seruca, R., Amorim, A., Ghibaudi, E. M.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 210 KB

english, 2007

7

Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3

Davidsson, J., Andersson, A., Paulsson, K., Heidenblad, M., Isaksson, M., Borg, A., Heldrup, J., Behrendtz, M., Panagopoulos, I., Fioretos, T., Johansson, B.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 604 KB

english, 2007

8

Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles

Beaumont, K. A., Shekar, S. L., Newton, R. A., James, M. R., Stow, J. L., Duffy, D. L., Sturm, R. A.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 502 KB

english, 2007

9

An SNP in the 5'-UTR of GDF5 is associated with osteoarthritis susceptibility in Europeans and with in vivo differences in allelic expression in articular cartilage

Southam, L., Rodriguez-Lopez, J., Wilkins, J. M., Pombo-Suarez, M., Snelling, S., Gomez-Reino, J. J., Chapman, K., Gonzalez, A., Loughlin, J.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 188 KB

english, 2007

10

Regulatory region single nucleotide polymorphisms of the apolipoprotein E gene and the rate of cognitive decline in Alzheimer's disease

Belbin, O., Dunn, J. L., Ling, Y., Morgan, L., Chappell, S., Beaumont, H., Warden, D., Smith, D. A., Kalsheker, N., Morgan, K.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 451 KB

english, 2007

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