B. Ferguson

发表

Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations.

J. Zonana, A. Monreal, B. Ferguson, 1998, American journal of human genetics.

Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain.

N. Brockdorff, J. Zonana, E. Formstone, 1997, Human molecular genetics.

Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations.

J. Orange, R. Geha, J. Strominger, 2002, The Journal of clinical investigation.

Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis.

J. Tschopp, P. Schneider, P. Overbeek, 2000, Development.

Gene defect in ectodermal dysplasia implicates a death domain adapter in development

M. Justice, J. Zonana, P. Overbeek, 2001, Nature.

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

J. Zonana, P. Overbeek, D. Headon, 1999, Nature Genetics.

Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications.

A. Clarke, J. Zonana, B. Ferguson, 1998, Journal of medical genetics.

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO).

S. Orlow, M. Golabi, J. Zonana, 2000, American journal of human genetics.

X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

D. Schlessinger, A. Chapelle, J. Kere, 1996, Nature Genetics.

Deficient natural killer cell cytotoxicity in patients with IKK-γ/NEMO mutations

J. Orange, R. Geha, J. Strominger, 2002 .

Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia

N. Morris, J. Zonana, H. Bächinger, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Mutations Leading to X-linked Hypohidrotic Ectodermal Dysplasia Affect Three Major Functional Domains in the Tumor Necrosis Factor Family Member Ectodysplasin-A*

J. Tschopp, P. Schneider, A. Tardivel, 2001, The Journal of Biological Chemistry.

Evolutionary and Biomedical Insights from the Rhesus Macaque Genome

David N. Messina, Ryan D. Hernandez, Jeffery P. Demuth, 2007, Science.