Louise M Kelly

Learn More
The recessive mouse mutation kreisler affects hindbrain segmentation and inner ear development in homozygous mice. The mouse gene affected by the mutation was found to encode a basic domain leucine-zipper (bZIP)-type transcription factor of the Maf-family named kr (Cordes, S.P. and Barsh, G.S. (1994) Cell 79, 1025-1034). The avian bZIP transcription factor(More)
The genetic basis for the development of brainstem neurons that generate respiratory rhythm is unknown. Here we show that mice deficient for the transcription factor MafB die from central apnea at birth and are defective for respiratory rhythmogenesis in vitro. MafB is expressed in a subpopulation of neurons in the preBötzinger complex (preBötC), a putative(More)
We have developed a monoclonal antibody (4A7) directed against the C-terminus of the ataxin-2 protein that is involved in the polyglutamine neurodegenerative disorder spinocerebellar ataxia type 2. Comparison with other ataxin-2 antibodies showed that 4A7 specifically recognized ataxin-2. In contrast, a previously reported ataxin-2 antibody (15F6) did not(More)
The authors studied inclusion formation in vitro using transiently transfected PC12 cells, with epitope-tagged and untagged full-length and truncated wild-type and expanded ataxins -1, -2, -3, and -7. At 72 hours, no inclusions were seen with wild-type full-length or truncated ataxins -2, -3, or -7, and only one with ataxin-1. Truncation abolished nuclear(More)
This paper explores implicit learning in typically developing and primary school children (9-12 years old) with developmental dyslexia using an artificial grammar learning (AGL) task. Two experiments were conducted, which differed in time of presentation and nature of the instructional set (experiment 1--implicit instructions vs experiment 2--explicit(More)
Acute promyelocytic leukemia (APL) cells invariably express aberrant fusion proteins involving the retinoic acid receptor ␣ (RAR␣). The most common fusion partner is promyelocytic leukemia protein (PML), which is fused to RAR␣ in the balanced reciprocal chromosomal translocation, t(15;17)(q22:q11). Expression of PML͞ RAR␣ from the cathepsin G promoter in(More)
The main aim of this thesis is to provide insight into the interaction of the syntactic and pragmatic properties of German, particularly with respect to the issue of con-gurationality. This language is particularly diicult to classify as it displays both subject-object asymmetries (a feature of \conngurational" languages), but also has a topic position (a(More)
Recently, it has been suggested that anti-gliadin antibodies (αGAb) may produce “gluten ataxia”, even in the absence of celiac disease enteropathy. αGAb are reportedly present in 12–50 % of patients with sporadic ataxia, but also in 12 % of the general population, such that the importance of αGAb as a cause of sporadic ataxia is not conclusively settled. We(More)
Executive summary Rabies is a zoonotic viral disease that causes acute encephalitis in humans and other warm-blooded animals; it is the only disease with almost 100% mortality once clinical signs are present. Transmission is usually through saliva via the bite of an infected animal, with dogs being the main transmitter of rabies to humans. The World Health(More)
Most adult-onset sporadic ataxias are unexplained, and the claim that many of these may be a result of gluten sensitivity has led to uncertainty as to whether to test for anti-gliadin antibodies (αGAb) and, if present, whether to recommend a gluten-free diet or continue searching for other causes of ataxia. This uncertainty arises in part from the frequency(More)