Lista de obras -

A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate.

artículo científico publicado en 2000

A screen for RAS mutations in individuals at risk of secondary leukaemia due to occupational exposure to petrochemicals

scientific article published on 01 May 1995

Analysis of fish ZP1/ZPB homologous genes--evidence for both genome duplication and species-specific amplification models of evolution.

artículo científico publicado en 2003

Cracking the egg: increased complexity in the zona pellucida.

artículo científico publicado en 2005

Functional polymorphisms in the P2X7 receptor gene are associated with stress fracture injury

artículo científico publicado en 2016

Identification of novel breast cancer-associated transcripts by UniGene database mining and gene expression analysis in normal and malignant cells.

artículo científico publicado en 2012

Identification of the true human orthologue of the mouse Zp1 gene: evidence for greater complexity in the mammalian zona pellucida?

scientific article published on 01 October 1999

Increased Training Volume Improves Bone Density and Cortical Area in Adolescent Football Players.

artículo científico publicado en 2017

MIRs as agents of mammalian gene evolution.

artículo científico publicado en 2000

Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness.

artículo científico publicado en 1998

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment ⬇️

artículo científico publicado el 1 de mayo de 1998

Paradigms and paradoxes: mouse (and human) models of genetic deafness.

artículo científico publicado en 1997

RANK/RANKL/OPG pathway: genetic associations with stress fracture period prevalence in elite athletes.

artículo científico publicado en 2014

SNPs in the vicinity of P2X7R, RANK/RANKL/OPG and Wnt signalling pathways and their association with bone phenotypes in academy footballers.

artículo científico publicado en 2018

Svp1p defines a family of phosphatidylinositol 3,5-bisphosphate effectors

artículo científico publicado en 2004

The association of novel polymorphisms with stress fracture injury in Elite Athletes: Further insights from the SFEA cohort