David Baty

Geography of HFE C282Y and H63D Mutations

Hallmarks of Cancer: The Next Generation

Non-alcoholic steatohepatitis: a common cause of progressive chronic liver injury?

The tumor suppressor kinase LKB1: lessons from mouse models

Estrogen Receptors: How Do They Signal and What Are Their Targets

AMPK: guardian of metabolism and mitochondrial homeostasis

Accessories to the Crime: Functions of Cells Recruited to the Tumor Microenvironment

TGFβ signalling in context

High‐resolution 19p13.2–13.3 allelotyping of breast carcinomas demonstrates frequent loss of heterozygosity

Scaffold attachment factors SAFB1 and SAFB2: Innocent bystanders or critical players in breast tumorigenesis?

The human keratins: biology and pathology

The mini-driver model of polygenic cancer evolution

APC and the three-hit hypothesis

Diseases of epidermal keratins and their linker proteins

Clustering of mutations associated with mild Marfan-like phenotypes in the 3? region ofFBN1 suggests a potential genotype-phenotype correlation

Dysfunctional KEAP1–NRF2 Interaction in Non-Small-Cell Lung Cancer

An improved real time PCR method for simultaneous detection of C282Y and H63D mutations in the HFE gene associated with hereditary hemochromatosis

Human Splicing Finder: an online bioinformatics tool to predict splicing signals

The Importance of Race and Ethnic Background in Biomedical Research and Clinical Practice

LKB1; linking cell structure and tumor suppression

The molecular genetics of Marfan syndrome and related microfibrillopathies

Structural and regulatory functions of keratins

Genotype and Phenotype Analysis of 171 Patients Referred for Molecular Study of the Fibrillin-1 Gene FBN1 Because of Suspected Marfan Syndrome

The Natural History of Nonalcoholic Fatty Liver Disease: A Population-Based Cohort Study

Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues.

A comprehensive review of reported heritable noggin‐associated syndromes and proposed clinical utility of one broadly inclusive diagnostic term:NOG‐related‐symphalangism spectrum disorder (NOG‐SSD)

Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems

Safe management of surgical smoke in the age of COVID-19

Elastic fibres

Immediate and long-term impact of the COVID-19 pandemic on delivery of surgical services

Consenso colombiano de atención, diagnóstico y manejo de la infección por SARS-COV-2/COVID 19 en establecimientos de atención de la salud. Recomendaciones basadas en consenso de expertos e informadas en la evidencia

Minimally Invasive Surgery and the Novel Coronavirus Outbreak: Lessons Learned in China and Italy

Correlation of a recurrent FBN1 mutation (R122C) with an atypical familial marfan syndrome phenotype

Chromosomal changes in colorectal adenomas: Relationship to gene mutations and potential for clinical utility

Haemochromatosis mutations in North‐East Scotland

Growth and Skeletal Development in Families with <i>NOGGIN</i> Gene Mutations

Epidermolysis Bullosa Simplex in Israel

An investigation of the Peutz-Jeghers gene (LKB1) in sporadic breast and colon cancers

Chemical composition of smoke produced by high-frequency electrosurgery in a closed gaseous environment

Epidermolysis Bullosa Simplex in Scotland Caused by a Spectrum of Keratin Mutations

A Heterozygous Frameshift Mutation in the V1 Domain of Keratin 5 in a Family with Dowling–Degos Disease

Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis.