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Jennifer M. Love

Researcher at Auckland City Hospital

Publications -  35
Citations -  2409

Jennifer M. Love is an academic researcher from Auckland City Hospital. The author has contributed to research in topics: Gene & Genome. The author has an hindex of 12, co-authored 35 publications receiving 2361 citations. Previous affiliations of Jennifer M. Love include John Radcliffe Hospital & Massachusetts Institute of Technology.

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Genetic analysis of autoimmune type 1 diabetes mellitus in mice.

TL;DR: In this article, a genetic map of the mouse genome, analysed using the polymerase chain reaction, has been assembled specifically for the study of autoimmune type 1 diabetes in the nonobese diabetic mouse.
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Towards construction of a high resolution map of the mouse genome using PCR-analysed microsatellites

TL;DR: Fifty sequences from the mouse genome database containing simple sequence repeats or microsatellites have been analysed for size variation using the polymerase chain reaction and gel electrophoresis to facilitate construction of high resolution maps of both the mouse and human genomes.
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Metastable Pluripotent States in NOD-Mouse-Derived ESCs

TL;DR: It is found that NOD stem cells can be stabilized by providing constitutive expression of Klf4 or c-Myc or small molecules that can replace these factors during in vitro reprogramming, which suggests that stem cells from different genetic backgrounds can assume distinct states of pluripotency in vitro.
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The molecular mechanism of phase variation of H. influenzae lipopolysaccharide.

TL;DR: Multiple carbohydrate structures on the outer-membrane lipopolysaccharide (LPS) of the gram-negative pathogen H. influenzae undergo high frequency, reversible loss, indicative of phase variation.
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Crosses of Nod Mice with the Related Non Strain - a Polygenic Model for Iddm

TL;DR: This study shows that the diabetogenic phenotype can be achieved through the actions of variable combinations of MHC-unlinked genes and a diabetogenesis MHC haplotype through outcrossing NOD mice to other inbred strains congenic for the NOD M HC haplotype.