Predictors of Mortality and Morbidity in Clostridium Difficile Infection (2009)
Background: Clostridium Difficile (CD) is implicated in 20 to 30% of patients with antibiotic-associated diarrhoea, in 50 to 70% of those with antibiotic-associated colitis and in more than 90% of...
Richardson, Rebecca J., Dixon, Jill, Jiang, Rulang, Dixon, Michael J.
In mammals, adhesion and fusion of the palatal shelves are essential mechanisms during the development of the secondary palate; failure of these processes leads to the congenital anomaly, cleft...
Service level agreements (SLAs) are becoming an increasingly popular way to manage the quality of services within organisations. Monash University is developing SLA's between central support...
The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation (2005)
Gonzales, Bianca, Henning, Dale, So, Rolando B., Dixon, Jill, Dixon, Michael J., Valdez, Benigno C.
Treacher Collins syndrome (TCS) is characterized by defects in craniofacial development, which results from mutations in the TCOF1 gene. TCOF1 encodes the nucleolar phosphoprotein treacle, which...
Dixon, Jill, Ellis, Ian, Bottani, Armand, Temple, Karen, Dixon, Michael James
Treacher Collins syndrome (TCS) is an autosomal dominant disorder of facial development, which results from mutations in TCOF1. TCS comprises conductive hearing loss, hypoplasia of the mandible and...
Mutation of the gene encoding fibrillin-2 results in syndactyly in mice (2001)
Chaudhry, Shazia S., Gazzard, James, Baldock, Clair, Dixon, Jill, Rock, Matthew J., Skinner, Gail C., ...
Fibrillins are large, cysteine-rich glycoproteins that form microfibrils and play a central role in elastic fibrillogenesis. Fibrillin-1 and fibrillin-2, encoded by FBN1 on chromosome 15q21.1 and...
Dixon, Jill, Brakebusch, Cord, Fässler, Reinhard, Dixon, Michael J.
Treacher Collins syndrome (TCS) is an autosomal dominant disorder of human craniofacial development that results from loss-of-function mutations in the gene TCOF1. Although this gene has been...
Dixon, Michael J., Dixon, Jill, Raskova, Dagmar, Le Beau, Michelle M., Williamson, Robert, Kinger, Katherine, ...
Treacher Collins syndrome (TCOF1) is an autosomal dominant disorder of craniofacial development, the locus for which has been chromosomally localized to 5q31-34. We have isolated four hypervarlable...
Characterization of the Nucleolar Gene Product, Treacle, in Treacher Collins Syndrome
Isaac, Cynthia, Marsh, Karen L., Paznekas, William A., Dixon, Jill, Dixon, Michael J., Jabs, Ethylin Wang, ...
Treacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development caused by mutations in the gene TCOF1. Its gene product, treacle, consists mainly of a central repeat...
Valdez, Benigno C., Henning, Dale, So, Rolando B., Dixon, Jill, Dixon, Michael J.
Treacher Collins syndrome (TCS) is an autosomal dominant disorder characterized by an abnormality of craniofacial development that arises during early embryogenesis. TCS is caused by mutations in the...
Wang, Xin, Merritt, Anita J., Seyfried, Jan, Guo, Chun, Papadakis, Emmanouil S., Finegan, Katherine G., ...
To elucidate the physiological significance of MEK5 in vivo, we have examined the effect of mek5 gene elimination in mice. Heterozygous mice appear to be healthy and were fertile. However,...
Characterization of the Nucleolar Gene Product, Treacle, in Treacher Collins Syndrome
Isaac, Cynthia, Marsh, Karen L., Paznekas, William A., Dixon, Jill, Dixon, Michael J., Jabs, Ethylin Wang, ...
Treacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development caused by mutations in the gene TCOF1. Its gene product, treacle, consists mainly of a central repeat...
Valdez, Benigno C., Henning, Dale, So, Rolando B., Dixon, Jill, Dixon, Michael J.
Treacher Collins syndrome (TCS) is an autosomal dominant disorder characterized by an abnormality of craniofacial development that arises during early embryogenesis. TCS is caused by mutations in the...
Wang, Xin, Merritt, Anita J., Seyfried, Jan, Guo, Chun, Papadakis, Emmanouil S., Finegan, Katherine G., ...
To elucidate the physiological significance of MEK5 in vivo, we have examined the effect of mek5 gene elimination in mice. Heterozygous mice appear to be healthy and were fertile. However,...
Dixon, Jill, Jones, Natalie C., Sandell, Lisa L., Jayasinghe, Sachintha M., Crane, Jennifer, Rey, Jean-Philippe, ...
Neural crest cells are a migratory cell population that give rise to the majority of the cartilage, bone, connective tissue, and sensory ganglia in the head. Abnormalities in the formation,...
Richardson, Rebecca J., Dixon, Jill, Jiang, Rulang, Dixon, Michael J.
In mammals, adhesion and fusion of the palatal shelves are essential mechanisms during the development of the secondary palate; failure of these processes leads to the congenital anomaly, cleft...