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121.
Gloeckner, C.J. et al.: The parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity. Hum. Mol. Genet. 15, 223-232 (2006)
122.
Huang, K.M.* et al.: Xcat, a novel mouse model for Nance-Horan syndrome inhibits expression of the cytoplasmic-targeted Nhs1 isoform. Hum. Mol. Genet. 15, 319-327 (2006)
123.
Riemenschneider, M.* et al.: A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer's disease. Hum. Mol. Genet. 15, 2446-2456 (2006)
124.
Schaeffer, L. et al.: Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids Hum. Mol. Genet. 15, 1745-1756 (2006)
125.
Benet-Pagès, A. ; Orlik, P.* ; Strom, T.M. & Lorenz-Depiereux, B.: An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia. Hum. Mol. Genet. 14, 385-390 (2005)
126.
Hysi, P.* et al.: NOD1 variation, immunoglobulin E and asthma. Hum. Mol. Genet. 14, 935-941 (2005)
127.
Rivera, A.* et al.: Hypoethical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk. Hum. Mol. Genet. 14, 3227-3236 (2005)
128.
Rafalska, I.* et al.: The intranuclear localization and function of YT521-B is regulated by tyrosine phosphorylation. Hum. Mol. Genet. 13, 1535-1549 (2004)
129.
Hörtnagel, K. ; Prokisch, H.* & Meitinger, T.: An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria. Hum. Mol. Genet. 12, 321-327 (2003)
130.
Duetsch, G. et al.: STAT6 as an asthma candidate gene : Polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study. Hum. Mol. Genet. 11, 613-621 (2002)
131.
Palmer, L.J.* et al.: Meta-analysis for linkage to asthma and atopy in the chromosome 5q31-33 candidate region. Hum. Mol. Genet. 10, 891-899 (2001)
132.
Grimm, C. et al.: Isolation and embryonic expression of the novel mouse gene Hic1, the homologue of HIC1, a canditate gene for the Miller-Dieker syndrome. Hum. Mol. Genet. 8, 697-710 (1999)
133.
Becker, K.-F. et al.: Exon Skipping in the E-Cadherin Gene Transcript in Metastatic Human Gastric Carcinomas. Hum. Mol. Genet. 2, 803-804 (1993)
134.
Becker, K.F. et al.: Exon skipping in the E-cadherin gene transcript in metastatic human gastric carcinomas. Hum. Mol. Genet. 2, 803-804 (1993)
135.
Joos, S. et al.: Variable breakpoints in Burkitt lymphoma cells with chromosomal t(8;14) translocation separate c-myc and the IgH locus up to several hundred kb. Hum. Mol. Genet. 1, 625-632 (1992)
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