A. E. Trezíse

发表

Non-PCR methods for the analysis of CFTR transcripts.

M. Amaral, N. Mouchel, A. Harris, 2004, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Disrupted posttranscriptional regulation of the cystic fibrosis transmembrane conductance regulator (CFTR) by a 5′UTR mutation is associated with a cftr‐related disease

Cristina Bombieri, S. Lukowski, A. E. Trezíse, 2011, Human mutation.

Cystic fibrosis mice have arrived!

C. Higgins, A. E. Trezíse, 1992, Human molecular genetics.

The multidrug resistance and cystic fibrosis genes have complementary patterns of epithelial expression.

C. Higgins, A. E. Trezíse, S. Hyde, 1992, The EMBO journal.

Developmental regulation of the gradient of cftr expression in the rabbit heart

A. E. Trezíse, J. Vandenberg, Kevin R Wong, 2000, Mechanisms of Development.

Cloning and sequencing of cDNA encoding baboon liver alcohol dehydrogenase: evidence for a common ancestral lineage with the human alcohol dehydrogenase beta subunit and for class I ADH gene duplications predating primate radiation.

I. Beacham, A. E. Trezíse, R. Holmes, 1989, Proceedings of the National Academy of Sciences of the United States of America.

FK 506 and rapamycin do not affect platelet aggregation or mitochondrial function.

A. E. Trezíse, V. Pelekanou, J. Kay, 1991, Transplantation proceedings.

Properties of the cAMP‐activated C1‐ current in choroid plexus epithelial cells isolated from the rat.

A. E. Trezíse, P. Brown, J. Kibble, 1996, The Journal of physiology.

Testis-specific, alternative splicing of rodent CFTR mRNA.

C. Higgins, A. E. Trezíse, M. Buchwald, 1993, Human molecular genetics.

The origins of colour vision in vertebrates

A. E. Trezíse, S. Collin, 2004, Clinical & experimental optometry.

Expression of the cystic fibrosis gene in human foetal tissues.

S. Gould, A. E. Trezíse, S. Gould, 1993, Human molecular genetics.

In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator

M. Buchwald, A. E. Trezíse, 1991, Nature.

CFTR expression is regulated during both the cycle of the seminiferous epithelium and the oestrous cycle of rodents

M. Griswold, A. E. Trezíse, E. Thompson, 1993, Nature Genetics.

Localization of the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) in the rat to chromosome 4 and implications for the evolution of mammalian chromosomes.

M. Buchwald, A. E. Trezíse, C. Szpirer, 1992, Genomics.

Ferrets exclusively synthesize Neu5Ac and express naturally humanized influenza A virus receptors

L. Hartley-Tassell, S. Grimmond, S. Lukowski, 2014, Nature Communications.

Visual pigments in a living fossil, the Australian lungfish Neoceratodus forsteri

A. E. Trezíse, S. Collin, W. L. Davies, 2007, BMC Evolutionary Biology.

Evidence for three genes encoding class-I alcohol dehydrogenase subunits in baboon and analysis of the 5' region of the gene encoding the ADH beta subunit.

I. Beacham, A. E. Trezíse, R. Holmes, 1991, Gene.

Developmental expression of mucin genes MUC1 and MUC2.

M. Hollingsworth, A. E. Trezíse, A. Harris, 1994, Journal of cell science.

Tissue-specific in vivo transcription start sites of the human and murine cystic fibrosis genes.

C. Higgins, A. E. Trezíse, N. White, 1998, Human molecular genetics.

Tamoxifen blocks chloride channels. A possible mechanism for cataract formation.

C. Higgins, A. E. Trezíse, M. Valverde, 1994, The Journal of clinical investigation.

In vivo gene expression: DNA electrotransfer.

W. Colledge, A. E. Trezíse, W. L. Davies, 2003, Current opinion in molecular therapeutics.

In vivo DNA electrotransfer.

A. E. Trezíse, 2002, DNA and cell biology.

The optics of the growing lungfish eye: Lens shape, focal ratio and pupillary movements in Neoceratodus forsteri (Krefft, 1870)

A. E. Trezíse, S. Collin, H. Bailes, 2007, Visual Neuroscience.

The number, morphology, and distribution of retinal ganglion cells and optic axons in the Australian lungfish Neoceratodus forsteri (Krefft 1870)

A. E. Trezíse, S. Collin, H. Bailes, 2006, Visual Neuroscience.

Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a

Jamie I Vandenberg, Klaus Benndorf, Richard C Saumarez, 2002, Proceedings of the National Academy of Sciences of the United States of America.

In vitro and in vivo MMP gene expression localisation by In Situ-RT-PCR in cell culture and paraffin embedded human breast cancer cell line xenografts

L. Haupt, L. Griffiths, A. E. Trezíse, 2006, BMC Cancer.

Co-ordinate regulation of the cystic fibrosis and multidrug resistance genes in cystic fibrosis knockout mice.

T. Freeman, C. Higgins, M. Evans, 1997, Human molecular genetics.

Post-transcriptional regulation of the cystic fibrosis gene in cardiac development and hypertrophy.

A. E. Trezíse, W. L. Davies, J. Vandenberg, 2004, Biochemical and biophysical research communications.

CFTR mRNA expression is regulated by an upstream open reading frame and RNA secondary structure in its 5' untranslated region.

S. Lukowski, A. E. Trezíse, J. Rothnagel, 2015, Human molecular genetics.

Cardiac Expression of the Cystic Fibrosis Transmembrane Conductance Regulator Involves Novel Exon 1 Usage to Produce a Unique Amino-terminal Protein*

A. E. Trezíse, W. L. Davies, J. Vandenberg, 2004, Journal of Biological Chemistry.

DNA Profiling of Horse Urine Samples to Confirm Donor Identity

A. E. Trezíse, P. Hawthorne, J. Cawdell-Smith, 2009 .

Exquisite and Multilevel Regulation of CFTR Expression

A. E. Trezíse, 2006 .

Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy

C. Higgins, M. Evans, W. Colledge, 1993, Nature.

Complementation of null CF mice with a human CFTR YAC transgene

M. Evans, W. Colledge, K. Kasschau, 1997, The EMBO journal.

Genetic regulation of laryngeal muscle development and differentiation

B. Murdoch, A. E. Trezíse, 2001 .

Molecular and functional distributions of chloride conductances in rabbit ventricle.

S. Bryant, A. E. Trezíse, G. Hart, 1999, American journal of physiology. Heart and circulatory physiology.