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Gene variants associated with ischemic stroke: the cardiovascular health stud...

Luke(May M),O'Meara(Ellen S),Rowland(Charl... Stroke 2009-02-20

...DMXL2, and ABCG2) were nominally associated with stroke (one-sided P<0.05, false discovery rate=0.55). The Val12Met SNP ...

Regional rearrangements in chromosome 15q21 cause formation of cryptic promot...

Demura(Masashi),Martin(Regina M),Shozu(Mak... Hum Mol Genet 2007-12-27

...DMXL2), normally transcribed from the same strand, closer to CYP19. The proximal breakpoints of inversions were located ...

Genome-Wide Functional Annotation of Human Protein-Coding Splice Variants Usi...

Panwar(Bharat),Menon(Rajasree),Eksi(Ridvan... J Proteome Res 0000-00-00

...DMXL2 genes. All predictions have been implemented in a web resource called "IsoFunc", which is freely available for the...

A dominant variant in DMXL2 is linked to nonsyndromic hearing loss.

Chen(Dong-Ye),Liu(Xing-Feng),Lin(Xiao-Jian... Genet Med 0000-00-00

...DMXL2 as the only candidate pathogenic variant segregating the hearing loss. In mouse cochlea, expression of DMXL2 was r...

Dynamic Regulation of Hypothalamic DMXL2, KISS1, and RFRP Expression During P...

Wahab(Fazal),Drummer(Charis),Schlatt(Stefa... Mol Neurobiol 0000-00-00

...DMXL2 in the regulation of reproduction, we analyzed the expression of DMXL2 in hypothalami of newborn, infantile, juven...

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