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Lista de obras de Martin A. Kennedy

35th Annual Meeting of the European Association for the Study of Diabetes

artículo científico

35th Annual Meeting of the European Association for the Study of Diabetes : Brussels, Belgium, 28 September-2 October 1999

article

A New Zealand platform to enable genetic investigation of adverse drug reactions

artículo científico publicado en 2017

A common P-glycoprotein polymorphism is associated with nortriptyline-induced postural hypotension in patients treated for major depression

artículo científico publicado en 2002

A complex chromosome rearrangement forms the BCR-ABL fusion gene in leukemic cells with a normal karyotype

artículo científico publicado en 1991

A dopamine transporter polymorphism is a risk factor for borderline personality disorder in depressed patients

artículo científico publicado en 2006

A genome project for Māori and Pasifika: charting a path to equity in genomic medicine for Aotearoa

scientific article published on 17 August 2018

A genome-wide association study of anorexia nervosa

artículo científico publicado en 2014

A large-scale genome-wide association study meta-analysis of cannabis use disorder

artículo científico publicado en 2020

A multiplex pharmacogenetics assay using the MinION nanopore sequencing device

artículo científico publicado en 2019

A multiplexed allele-specific polymerase chain reaction assay for the detection of common thiopurine S-methyltransferase (TPMT) mutations

artículo científico publicado en 2004

A polymorphism in the dopamine beta-hydroxylase gene is associated with "paranoid ideation" in patients with major depression

artículo científico publicado en 2002

A polymorphism of the GTP-cyclohydrolase I feedback regulator gene alters transcriptional activity and may affect response to SSRI antidepressants

artículo científico publicado en 2010

A proof-of-principle study of the short-term effects of 3,4-methylenedioxymethamphetamine (MDMA) on tinnitus and neural connectivity

scientific article published on 06 January 2020

A sequence homologous to kappa-deleting element is located 5' to the human JK locus

artículo científico publicado en 1989

A validation of Illumina EPIC array system with bisulfite-based amplicon sequencing

artículo científico publicado en 2021

ANGI - Anorexia Nervosa Genetics Initiative

artículo científico publicado en 2020

Age-dependent antidepressant pharmacogenomics: polymorphisms of the serotonin transporter and G protein beta3 subunit as predictors of response to fluoxetine and nortriptyline

artículo científico publicado en 2003

Allele frequencies of thiopurine S-methyltransferase (TPMT) variants in the Nigerian population

Allele frequency differences of cytochrome P450 polymorphisms in a sample of New Zealand Māori.

artículo científico publicado en 2008

Allelic Dropout During Polymerase Chain Reaction due to G-Quadruplex Structures and DNA Methylation Is Widespread at Imprinted Human Loci.

artículo científico publicado en 2017

An association study of DRD2 and COMT polymorphisms with novelty seeking and harm avoidance scores, in two independent samples of depressed patients

artículo científico publicado en 2007

Analysis of DNA methylation associates the cystine-glutamate antiporter SLC7A11 with risk of Parkinson's disease

artículo científico publicado en 2020

Association between cytochrome P450 2D6 genotype and harm avoidance

artículo científico publicado en 2004

Association of a duplicated repeat polymorphism in the 5'-untranslated region of the DRD4 gene with novelty seeking

artículo científico publicado en 2004

Association of a functional polymorphism in the adrenomedullin gene (ADM) with response to paroxetine

artículo científico publicado en 2009

Associations between schizophrenia genetic risk, anxiety disorders and manic/hypomanic episode in a longitudinal population cohort study

artículo científico publicado en 2019

Author Correction: Human gut microbiome changes during a 10 week Randomised Control Trial for micronutrient supplementation in children with attention deficit hyperactivity disorder

scientific article published on 21 January 2020

BCR gene recombines with genomically distinct sites on band 11Q13 in complex BCR-ABL translocations of chronic myeloid leukemia.

artículo científico publicado en 1996

Basophils (Bsp-1+) derive from the leukemic clone in human myeloid leukemias involving the chromosome breakpoint 9q34.

artículo científico publicado en 1989

Basophils exhibit rearrangement of the bcr gene in Philadelphia chromosome-positive chronic myeloid leukemia

artículo científico publicado en 1988

Benzylpiperazine: a drug of abuse?

artículo científico publicado en 2007

Beta-adrenergic receptor polymorphisms and drug responses in asthma

artículo científico publicado en 2002

Beyond TPMT: genetic influences on thiopurine drug responses in inflammatory bowel disease

article

Bipolar disorder not otherwise specified: comparison with bipolar disorder I/II and major depression

artículo científico publicado en 2007

Breast Cancer and Tamoxifen: A Nigerian Perspective to Effective Personalised Therapy

artículo científico publicado en 2020

Broken heart syndrome - is it a psychosomatic disorder?

artículo científico publicado en 2014

Bronchodilator response in relation to beta2-adrenoceptor haplotype in patients with asthma

artículo científico publicado en 2005

CARD15 allele frequency differences in New Zealand Maori: ancestry specific susceptibility to Crohn's disease in New Zealand?

artículo científico publicado en 2006

CTG-repeat expansions in the DMPK gene do not cause takotsubo syndrome

artículo científico publicado en 2015

Can we predict treatment response in children with ADHD to a vitamin-mineral supplement? An investigation into pre-treatment nutrient serum levels, MTHFR status, clinical correlates and demographic variables

artículo científico publicado en 2018

Canterbury Health, Ageing and Life Course (CHALICE) study: rationale, design and methodology

artículo científico publicado el 31 de mayo de 2013

Choice of PCR microtube can impact on the success of long-range PCRs.

artículo científico publicado en 2015

Clinical implications of pharmacogenetic variation on the effects of statins.

artículo científico publicado en 2011

Cloning and sequencing of a t(14;19) breakpoint that involves the C mu switch region

artículo científico publicado en 1993

Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression.

artículo científico publicado en 2017

Common CYP2D6, CYP2C9, and CYP2C19 Gene Variants, Health Anxiety, and Neuroticism Are Not Associated With Self-Reported Antidepressant Side Effects

artículo científico publicado en 2019

Common Variants Coregulate Expression of GBA and Modifier Genes to Delay Parkinson's Disease Onset

scientific article published on 18 June 2020

Comparing the variants of takotsubo syndrome: an observational study of the ECG and structural changes from a New Zealand tertiary hospital

article

Complete Genome Sequence of Legionella sainthelensi Isolated from a Patient with Legionnaires' Disease

artículo científico publicado en 2018

Comprehensive Assessment of BARD1 Messenger Ribonucleic Acid Splicing With Implications for Variant Classification

artículo científico publicado en 2019

Confirmation of association of IRGM and NCF4 with ileal Crohn's disease in a population-based cohort

artículo científico publicado en 2008

Contrasting signals of cardiovascular health among natriuretic peptides in subjects without heart disease

artículo científico publicado en 2019

Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathy

artículo científico publicado en 2018

Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathy

article

Correlation of CYP2D6 genotype with perhexiline phenotypic metabolizer status

artículo científico publicado en 2003

Cross-Comparison of Exome Analysis, Next-Generation Sequencing of Amplicons, and the iPLEX(®) ADME PGx Panel for Pharmacogenomic Profiling

artículo científico publicado en 2016

Current State and Future Prospects of Direct-to-Consumer Pharmacogenetics ⬇️

artículo científico publicado el 20 de agosto de 2012

Cytochrome P450 2D6 genotype does not predict SSRI (fluoxetine or paroxetine) induced hyponatraemia

artículo científico publicado en 2002

DNA G-quadruplexes show strong interaction with DNA methyltransferases in vitro.

artículo científico publicado en 2016

DNA sequence analysis of the major breakpoint cluster region of the BCR gene rearranged in Philadelphia-positive human leukemias.

artículo científico publicado en 1993

DNA-based diagnostics for adrenoleukodystrophy in a large New Zealand family

artículo científico publicado en 1996

DUF1220 copy number is linearly associated with increased cognitive function as measured by total IQ and mathematical aptitude scores

artículo científico publicado en 2015

Determination of beta2-adrenergic receptor (ADRB2) haplotypes by a multiplexed polymerase chain reaction assay.

artículo científico publicado en 2002

Development of a predicted physical map of microsatellite locus positions for pinnipeds, with wider applicability to the Carnivora

article

Dinucleotide repeat polymorphism for HLX1 gene

artículo científico publicado en 1994

Downregulation of Ccnd1 and Hes6 in rat hippocampus after chronic exposure to the antidepressant paroxetine

artículo científico publicado en 2008

Effect of 7,8-dihydroneopterin mediated CD36 down regulation and oxidant scavenging on oxidised low-density lipoprotein induced cell death in human macrophages.

artículo científico publicado en 2017

Effect of genetic factors on the response to vitamin D3 supplementation in the VIDARIS randomized controlled trial

scientific article published on 12 February 2020

Effect of inflammatory bowel disease classification changes on NOD2 genotype–phenotype associations in a population-based cohort

artículo científico publicado en 2007

Effect of insulating existing houses on health inequality: cluster randomised study in the community

artículo científico publicado en 2007

Epigenetics, nutrition and mental health. Is there a relationship?

artículo científico publicado en 2017

Erratum to: Impact of New Genomic Technologies on Understanding Adverse Drug Reactions

artículo científico publicado en 2016

Estimating the heritability of reporting stressful life events captured by common genetic variants

artículo científico publicado en 2012

Examining the role of components of Slc11a1 (Nramp1) in the susceptibility of New Zealand sea lions (Phocarctos hookeri) to disease

artículo científico publicado en 2015

Exome sequencing and array-based comparative genomic hybridisation analysis of preferential 6-methylmercaptopurine producers

scientific article published on 10 March 2015

Expression and association analyses of promoter variants of the neurogenic gene HES6, a candidate gene for mood disorder susceptibility and antidepressant response

artículo científico publicado en 2009

Extensive variation at MHC DRB in the New Zealand sea lion (Phocarctos hookeri) provides evidence for balancing selection.

artículo científico publicado en 2013

FAT and bipolar affective disorder

artículo científico publicado en 2007

Fluorescence Methods for Probing G-Quadruplex Structure in Single- and Double-Stranded DNA.

artículo científico publicado en 2016

Fragile X mental retardation syndrome: DNA diagnosis and carrier detection in New Zealand families.

artículo científico publicado en 1995

G-quadruplex structures and CpG methylation cause drop-out of the maternal allele in polymerase chain reaction amplification of the imprinted MEST gene promoter

artículo científico publicado en 2014

G-quadruplex structures bind to EZ-Tn5 transposase

scientific article published on 14 August 2020

Gene expression effects of lithium and valproic acid in a serotonergic cell line

article

Gene expression effects of lithium and valproic acid in a serotonergic cell line

artículo científico publicado en 2018

Gene transfer between Salmonella enterica serovar Typhimurium inside epithelial cells

artículo científico publicado en 2002

Genes, environments, and developmental research: methods for a multi-site study of early substance abuse

artículo científico publicado en 2013

Genetic Evidence of a Population Bottleneck and Inbreeding in the Endangered New Zealand Sea Lion, Phocarctos hookeri

artículo científico publicado en 2016

Genetic association study of childhood aggression across raters, instruments, and age

artículo científico publicado en 2021

Genetic, developmental and personality correlates of self-mutilation in depressed patients

artículo científico publicado en 2006

Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

scholarly article

Genome-Wide Meta-Analysis of Longitudinal Alcohol Consumption Across Youth and Early Adulthood

artículo científico publicado en 2015

Genome-wide DNA methylation analysis of heavy cannabis exposure in a New Zealand longitudinal cohort

scientific article published on 22 April 2020

Genome-wide DNA methylation analysis of heavy cannabis exposure in a New Zealand longitudinal cohort

artículo científico publicado en 2019

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

artículo científico publicado en 2019

Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder

artículo científico publicado en 2011

Genome-wide impact of hydrogen peroxide on maintenance DNA methylation in replicating cells

artículo científico publicado en 2021

Genomic structure, promoter sequence, and revised translation of human homeobox gene HLX1.

artículo científico publicado en 1994

HRAS1 and INS genes are relocated but not structurally altered as a result of the t(7;11) (p15;p15) in a clone from a patient with acute myeloid leukaemia (M4)

article

Heavier smoking may lead to a relative increase in waist circumference: evidence for a causal relationship from a Mendelian randomisation meta-analysis. The CARTA consortium

artículo científico publicado en 2015

Heterozygote advantage at MHC DRB may influence response to infectious disease epizootics

artículo científico publicado en 2015

How the pharmacogenetics of cytochrome P450 enzymes may affect prescribing

artículo científico publicado en 2002

Human gut microbiome changes during a 10 week Randomised Control Trial for micronutrient supplementation in children with attention deficit hyperactivity disorder

artículo científico publicado en 2019

IL23R R381Q and ATG16L1 T300A Are Strongly Associated With Crohn's Disease in a Study of New Zealand Caucasians With Inflammatory Bowel Disease

article

IMPDH1 promoter mutations in a patient exhibiting azathioprine resistance.

artículo científico publicado en 2006

Identification of P gene mutations in individuals with oculocutaneous albinism in sub-saharan africa; robyn kerr, gwynneth stevens, prashiela manga, sarah salm, premila john, tabitha haw, and michele ramsay; (Article was originally published in huma

artículo científico publicado en 2000

Ile164 variant of β2-adrenoceptor does not influence outcome in heart failure but may interact with β blocker treatment

artículo científico publicado en 2008

Impact of New Genomic Technologies on Understanding Adverse Drug Reactions

artículo científico publicado en 2016

Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing

scientific article published on 23 August 2019

Incidence of Mycobacterium avium subspecies paratuberculosis in a population-based cohort of patients with Crohn's disease and control subjects

artículo científico publicado en 2008

Increased risk of major depression by childhood abuse is not modified by CNR1 genotype

artículo científico publicado en 2012

Institutional profile: The Carney Centre for Pharmacogenomics: a New Zealand focus for personalized medicine research

artículo científico publicado en 2012

Inter-individual variation in imatinib disposition: any role for prevalent variants of CYP1A2, CYP2C8, CYP2C9, and CYP3A5 in Nigerian CML patients?

artículo científico publicado en 2018

Interactions among genes influencing bacterial recognition increase IBD risk in a population-based New Zealand cohort

artículo científico publicado en 2009

Investigating the possible causal association of smoking with depression and anxiety using Mendelian randomisation meta-analysis: the CARTA consortium

artículo científico publicado en 2014

Involvement of immunoglobulin heavy- and light-chain (kappa) gene clusters in a human B-cell translocation, t(2;14).

artículo científico publicado en 1989

Is cytochrome P450 2C9 genotype associated with NSAID gastric ulceration?

artículo científico publicado en 2001

Lack of association between HLA-G 14 bp insertion/deletion polymorphism and response to long-term therapy with methotrexate response in rheumatoid arthritis

artículo científico publicado en 2009

Lack of association between the ITPA 94C>A polymorphism and adverse effects from azathioprine

artículo científico publicado en 2004

Life stress, 5-HTTLPR and mental disorder: findings from a 30-year longitudinal study ⬇️

artículo científico publicado el 1 de febrero de 2011

Linking pharmacovigilance with pharmacogenetics

artículo científico publicado en 2004

Long Fragment Polymerase Chain Reaction.

artículo científico publicado en 2017

Low red cell folate levels are associated with poor response to nortriptyline in major depression

artículo científico publicado en 2007

MAOA, abuse exposure and antisocial behaviour: 30-year longitudinal study ⬇️

artículo científico publicado el 1 de junio de 2011

METHYLOME IMPACTS OF CANNABIS USE IN THE CHRISTCHURCH HEALTH AND DEVELOPMENT STUDY

artículo científico publicado en 2019

Mapping and regulation of the pifC promoter of the F plasmid

artículo científico publicado en 1988

Mean telomere length is not associated with current health status in a 50-year-old population sample

article

Mendelian Genetic Disorders

Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

artículo científico publicado en 2021

Methylated Cytosine Maintains G-Quadruplex Structures during Polymerase Chain Reaction and Contributes to Allelic Dropout.

artículo científico publicado en 2017

Methylomic changes in response to micronutrient supplementation and MTHFR genotype

artículo científico publicado en 2018

Metoclopramide-Induced Acute Dystonic Reactions May Be Associated With the CYP2D6 Poor Metabolizer Status and Pregnancy-Related Hormonal Changes

artículo científico publicado en 2019

Microsatellite polymorphisms associated with human behavioural and psychological phenotypes including a gene-environment interaction

artículo científico publicado en 2017

Moderating role of the MAOA genotype in antisocial behaviour ⬇️

artículo científico publicado el 1 de febrero de 2012

Multiplexed Nanopore Sequencing of HLA-B Locus in Māori and Pacific Island Samples

artículo científico publicado en 2018

Multiplexed nanopore sequencing of HLA-B locus in Māori and Polynesian samples

scholarly article

Mutations in the adrenoleukodystrophy gene

artículo científico publicado en 1997

Nanopore sequencing of full-length BRCA1 mRNA transcripts reveals co-occurrence of known exon skipping events

artículo científico publicado en 2017

Nanopore sequencing of the glucocerebrosidase (GBA) gene in a New Zealand Parkinson's disease cohort

scientific article published on 29 November 2019

Nanopore sequencing of the pharmacogene CYP2D6 allows simultaneous haplotyping and detection of duplications

scientific article published on 01 September 2019

No association between mean telomere length and life stress observed in a 30 year birth cohort

artículo científico publicado en 2014

No association between novelty seeking and the type 4 dopamine receptor gene (DRD4) in two New Zealand samples

artículo científico publicado en 1998

No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort.

artículo científico publicado en 2013

No evidence of increased adverse drug reactions in cytochrome P450 CYP2D6 poor metabolizers treated with fluoxetine or nortriptyline

artículo científico publicado en 2004

Nomenclature for alleles of the thiopurine methyltransferase gene

artículo científico publicado en 2013

Nonsynonymous Polymorphism in Guanine Monophosphate Synthetase Is a Risk Factor for Unfavorable Thiopurine Metabolite Ratios in Patients With Inflammatory Bowel Disease

artículo científico publicado en 2018

Novel CYP2D6 and CYP2C19 variants identified in a patient with adverse reactions towards venlafaxine monotherapy and dual therapy with nortriptyline and fluoxetine ⬇️

artículo científico publicado el 1 de septiembre de 2013

Novel chromosome translocation caused by fusion of immunoglobulin heavy and light chain V genes in a human B lymphoblastoid cell line.

artículo científico publicado en 1991

Novelty seeking and a dopamine transporter gene polymorphism (DAT1)

artículo científico publicado en 1997

Nucleotide sequence of an immunoglobulin D-J gene fusion from a B-cell prolymphocytic leukaemia.

artículo científico publicado en 1989

OPRM1 genotype and naltrexone response in depressed alcohol-dependent patients

artículo científico publicado en 2015

Orosomucoid influences both antidepressant tolerance and response

artículo científico publicado en 2006

Orosomucoid influences the response to antidepressants in major depressive disorder

artículo científico publicado en 2009

Outcome reporting in randomized trials in gout: A systematic scoping review from the OMERACT gout working group assessing the uptake of the core outcome set

artículo científico publicado en 2023

Penetrance and expressivity of the R858H CACNA1C variant in a five-generation pedigree segregating an arrhythmogenic channelopathy

article

Personalised prescribing in psychiatry: Has pharmacogenomics delivered on its promise?

artículo científico publicado en 2016

Ph-negative chronic myeloid leukemia: molecular analysis of ABL insertion into M-BCR on chromosome 22

scientific article published on 01 November 1990

PharmVar GeneFocus: CYP2D6

artículo científico publicado en 2019

Pharmacogenetics of Statin-Induced Myotoxicity

scientific article published on 16 October 2020

Pharmacogenetics of angiotensin-converting enzyme inhibitor-induced angioedema

artículo científico publicado en 2019

Pharmacogenomics: single genes, whole genomes and global networks

article

Polymorphisms in CYP2C8 and CYP3A5 genes in the Nigerian population

artículo científico publicado en 2016

Polymorphisms of DRD4 and DRD3 and risk of avoidant and obsessive personality traits and disorders

artículo científico publicado en 2003

Polymorphisms of sepiapterin reductase gene alter promoter activity and may influence risk of bipolar disorder

artículo científico publicado en 2009

Polymorphisms within the folate pathway predict folate concentrations but are not associated with disease activity in rheumatoid arthritis patients on methotrexate

artículo científico publicado en 2010

Preliminary evidence for an association between a dopamine D3 receptor gene variant and obsessive-compulsive personality disorder in patients with major depression

article

Prevalence and significance of CYP2C19*2 and CYP2C19*17 alleles in a New Zealand acute coronary syndrome population.

artículo científico publicado en 2015

Progressing the utilisation of pharmacogenetics and pharmacogenomics into clinical care

artículo científico

Proteomic analysis of embryonic stem cell–derived neural cells exposed to the antidepressant paroxetine

artículo científico publicado en 2008

Proteomic analysis of rat hippocampus exposed to the antidepressant paroxetine

scientific journal article

Rapid Detection of Common CARD15 Variants in Patients with Inflammatory Bowel Disease

Rapid and comprehensive determination of cytochrome P450 CYP2D6 poor metabolizer genotypes by multiplex polymerase chain reaction

artículo científico publicado en 2000

Rapid detection of common CARD15 variants in patients with inflammatory bowel disease

artículo científico publicado en 2004

Rapid detection of common cytochrome P450 2D6 alleles in Caucasians

artículo científico publicado en 2005

Relationship between metabolic phenotypes and genotypes of CYP1A2 and CYP2A6 in the Nigerian population.

artículo científico publicado en 2017

Relationships between angry-impulsive personality traits and genetic polymorphisms of the dopamine transporter

artículo científico publicado en 2009

Relevance of G-quadruplex structures to pharmacogenetics.

artículo científico publicado en 2014

Reversed diurnal variation in depression: associations with a differential antidepressant response, tryptophan: large neutral amino acid ratio and serotonin transporter polymorphisms

artículo científico publicado en 2005

Role of epigenetics in mental disorders

artículo científico publicado en 2008

Schizophrenia and bipolar affective disorder: perspectives for the development of therapeutics

artículo científico publicado en 2003

Self-mutilation and suicide attempts: relationships to bipolar disorder, borderline personality disorder, temperament and character

artículo científico publicado en 2010

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

artículo científico publicado en 2020

Stratification by smoking status reveals an association of CHRNA5-A3-B4 genotype with body mass index in never smokers

artículo científico publicado en 2014

Structural Analysis of G-Quadruplex Formation at the Human MEST Promoter

artículo científico publicado en 2017

Structure and Location of the Murine Adrenoleukodystrophy Gene

article

Telomere length measurement on the Roche LightCycler 480 Platform

artículo científico publicado en 2014

Testicular Cancer in New Zealand (TCNZ) study: protocol for a national case-control study

scholarly article

The Anorexia Nervosa Genetics Initiative: Overview and Methods

article

The Anorexia Nervosa Genetics Initiative: Study description and sample characteristics of the Australian and New Zealand arm.

artículo científico publicado en 2017

The Anorexia Nervosa: Genetics Initiative (ANGI): Australia and New Zealand join forces.

artículo científico publicado en 2015

The Driver of Extreme Human-Specific Olduvai Repeat Expansion Remains Highly Active in the Human Genome

artículo científico publicado en 2019

The Three Ps: Psychiatry, Pharmacy, and Pharmacogenomics, a Brief Report From New Zealand

artículo científico publicado en 2019

The anorexia nervosa genetics initiative (ANGI): Overview and methods

article

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

The oncogene ETS1 is distant from the chromosome 11 breakpoint in leukaemic cells with the t(11;19)(q23;p13).

artículo científico publicado en 1989

The presence of both serotonin 1A receptor (HTR1A) and dopamine transporter (DAT1) gene variants increase the risk of borderline personality disorder

artículo científico publicado en 2014

The sites of gene expression of atrial, brain, and C-type natriuretic peptides in mouse fetal development: temporal changes in embryos and placenta

artículo científico publicado en 1996

The use of low dose methotrexate in rheumatoid arthritis - are we entering a new era of therapeutic drug monitoring and pharmacogenomics?

artículo científico publicado en 2006

Thiopurine S-methyltransferase (TPMT) genotype does not predict adverse drug reactions to thiopurine drugs in patients with inflammatory bowel disease.

artículo científico publicado en 2003

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

artículo científico publicado en 2018

Transcriptional promoters in a replication region of F plasmid ⬇️

1986 doctoral thesis by Martin A. Kennedy at University of Auckland

Trinucleotide repeat variants in the promoter of the thiopurine S-methyltransferase gene of patients exhibiting ultra-high enzyme activity

artículo científico publicado en 2008

Tryptophan hydroxylase gene (TPH1) and peripheral tryptophan levels in depression

artículo científico publicado en 2008

Upstream genetic variant near INSIG2, influences response to carnitine supplementation in bipolar patients with valproate-induced weight gain

artículo científico publicado en 2009

Valproic acid exposure leads to upregulation and increased promoter histone acetylation of sepiapterin reductase in a serotonergic cell line

artículo científico publicado en 2015

[Letter to the Editor] Many commercial hot-start polymerases demonstrate activity prior to thermal activation

artículo científico publicado en 2016

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