P59 Hypokalemic paralysis as initial presentation in female patients with primary Sjogren's syndrome—a case series
Year: 2010
Type: conference-abstract
Abstract: Seven (Nod+Fix−) mutants of pea cv. Frisson were isolated following ethylmethane sulphonate mutagenesis. Histological, fluorescence and molecular approaches have been used to characterized symbiotic phenotypes and to classify the mutants. In all cases, Rhizobium infection occurred via root hairs and resulting nodules had a typical indeterminate structure. However, mutants could be broadly classified into two group on the basis of nodule development and the level of nodule-specific gene transcripts. In the first groups, comprising P12, P58, P61 and P63 lines, nodule development was approximately normal but was followed by premature senescence. In the second group comprising P59, P60 and P62, mutant lines showed an early arrest of nodule development. Developmentally-defective root hairs were also observed on roots of mutant P62.
Source: Indian Journal of Rheumatology
Authors: Paul T Antony, VS Negi, P Padhan, CB Mithun
Language: English
Subfield: Physiology (medical)
Field: Medicine
Domain: Health Sciences
Open Access status: diamond
OpenAlex ID: W2000335345