User profiles for "author:Tracey Weiler"
Tracey WeilerAssociate Professor, Department of Human and Molecular Genetics, Herbert Wertheim … Verified email at fiu.edu Cited by 2462 |
[HTML][HTML] Urine protein profiling with surface-enhanced laser-desorption/ionization time-of-flight mass spectrometry
Urine protein profiling with surface-enhanced laser-desorption/ionization time-of-flight mass
spectrometry. Background In the last few years there has been an increasing interest in …
spectrometry. Background In the last few years there has been an increasing interest in …
[PDF][PDF] Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin–ligase gene
Limb-girdle muscular dystrophy type 2H (LGMD2H) is a mild autosomal recessive myopathy
that was first described in the Manitoba Hutterite population. Previous studies in our …
that was first described in the Manitoba Hutterite population. Previous studies in our …
Proteomic-based detection of urine proteins associated with acute renal allograft rejection
S Schaub, D Rush, J Wilkins, IW Gibson… - Journal of the …, 2004 - journals.lww.com
At present, the diagnosis of renal allograft rejection requires a renal biopsy. Clinical
management of renal transplant patients would be improved by the development of non …
management of renal transplant patients would be improved by the development of non …
[HTML][HTML] Proteomic-based identification of cleaved urinary β2-microglobulin as a potential marker for acute tubular injury in renal allografts
Our aim is to develop noninvasive tests to monitor the renal allograft posttransplant.
Previously, we have reported that an unbiased proteomic-based approach can detect urine …
Previously, we have reported that an unbiased proteomic-based approach can detect urine …
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene (s)
T Weiler, R Bashir, LVB Anderson… - Human molecular …, 1999 - academic.oup.com
Limb girdle muscular dystrophy type 2B (LGMD2B) and Miyoshi myopathy (MM), a distal
muscular dystrophy, are both caused by mutations in the recently cloned gene dysferlin …
muscular dystrophy, are both caused by mutations in the recently cloned gene dysferlin …
The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1
SD Thompson, M Sudman, PS Ramos… - Arthritis & …, 2010 - Wiley Online Library
Objective To test for associations between non–major histocompatibility complex
susceptibility loci previously reported in autoimmune diseases and juvenile idiopathic …
susceptibility loci previously reported in autoimmune diseases and juvenile idiopathic …
[PDF][PDF] A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle …
T Weiler, CR Greenberg, T Zelinski, E Nylen… - The American Journal of …, 1998 - cell.com
Characterized by proximal muscle weakness and wasting, limb-girdle muscular dystrophies
(LGMDs) are a heterogeneous group of clinical disorders. Previous reports have …
(LGMDs) are a heterogeneous group of clinical disorders. Previous reports have …
Association of the 5-aminoimidazole-4-carboxamide ribonucleotide transformylase gene with response to methotrexate in juvenile idiopathic arthritis
A Hinks, H Moncrieffe, P Martin, S Ursu, S Lal… - Annals of the …, 2011 - ard.bmj.com
Objectives Methotrexate (MTX) is the mainstay treatment for juvenile idiopathic arthritis (JIA),
however approximately 30% of children will fail to respond to the drug. Identification of …
however approximately 30% of children will fail to respond to the drug. Identification of …
Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.
T Weiler, CR Greenberg, E Nylen… - American journal of …, 1996 - ncbi.nlm.nih.gov
We report the results of our investigations of a large, inbred, aboriginal Canadian kindred
with nine muscular dystrophy patients. The ancestry of all but two of the carrier parents could …
with nine muscular dystrophy patients. The ancestry of all but two of the carrier parents could …
Generation of novel pharmacogenomic candidates in response to methotrexate in juvenile idiopathic arthritis: correlation between gene expression and genotype
H Moncrieffe, A Hinks, S Ursu… - Pharmacogenetics …, 2010 - journals.lww.com
Objectives Little is known about the mechanisms of efficacy of methotrexate (MTX) in
childhood arthritis, or genetic influences upon response to MTX. The aims of this study were …
childhood arthritis, or genetic influences upon response to MTX. The aims of this study were …