Human Molecular Genetics

Abkürzung der Fachzeitschrift: HUM MOL GENET
ISSN: 0964-6906
Verlag: Oxford University Press (OUP): Policy B - Oxford Open Option B



Publikationen

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Heftnummer: 9, Band: 26, Seitenbereich: 1716-1731
Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations (2017)
Kosfeld A, Brand F, Weiss AC, et al.

Heftnummer: 7, Band: 26, Seitenbereich: 1230-1246
Therapeutic potential of AAV-mediated MMP-3 secretion from corneal endothelium in treating glaucoma (2017)
O'Callaghan J, Crosbie DE, Cassidy PS, et al.

Heftnummer: 17, Band: 25, Seitenbereich: 3863-3876
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression (2016)
Wyszynski A, Hong CC, Lam K, et al.

Heftnummer: 24, Band: 25, Seitenbereich: 5490-5499
Prostate cancer risk regions at 8q24 and 17q24 are differentially associated with somatic TMPRSS2:ERG fusion status (2016)
Luedeke M, Rinckleb AE, Fitzgerald LM, et al.

Heftnummer: 10, Band: 24, Seitenbereich: 2966-84
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2 (2015)
Orr N, Dudbridge F, Dryden N, et al.

Heftnummer: 5, Band: 24, Seitenbereich: 1478-92
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk (2015)
Painter JN, O'Mara TA, Batra J, et al.

Heftnummer: 22, Band: 24, Seitenbereich: 6552-63
Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus (2015)
Hauser MA, Aboobakar IF, Liu Y, et al.

Heftnummer: 1, Band: 24, Seitenbereich: 285-98
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk (2015)
Lin WY, Camp NJ, Ghoussaini M, et al.


Zuletzt aktualisiert 2015-29-05 um 16:45