Michaela Kendall

Edgbaston, ENG B152TT, United Kingdom

Last Updated: 09/26/2026

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Found 22 publications

Long-term monitoring for nanomedicine implants and drugs.

Long-term monitoring for nanomedicine implants and drugs.

Journal: Nature nanotechnology

Published: March 04, 2016

Surfactant protein A (SP-A) inhibits agglomeration and macrophage uptake of toxic amine modified nanoparticles.

Surfactant protein A (SP-A) inhibits agglomeration and macrophage uptake of toxic amine modified nanoparticles.

Journal: Nanotoxicology

Published: February 14, 2015

Nanoparticles modulate surfactant protein A and D mediated protection against influenza A infection in vitro.

Nanoparticles modulate surfactant protein A and D mediated protection against influenza A infection in vitro.

Journal: Philosophical transactions of the Royal Society of London. Series B, Biological sciences

Published: December 24, 2014

Nanoparticle growth and surface chemistry changes in cell-conditioned culture medium.

Nanoparticle growth and surface chemistry changes in cell-conditioned culture medium.

Journal: Philosophical transactions of the Royal Society of London. Series B, Biological sciences

Published: December 24, 2014

'Bio-nano interactions: new tools, insights and impacts': summary of the Royal Society discussion meeting.

'Bio-nano interactions: new tools, insights and impacts': summary of the Royal Society discussion meeting.

Journal: Philosophical transactions of the Royal Society of London. Series B, Biological sciences

Published: December 24, 2014

A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect.

A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect.

Journal: Endocrine research

Published: October 21, 2014

One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism.

One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism.

Journal: Journal of clinical research in pediatric endocrinology

Published: September 23, 2014

An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.

An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: January 29, 2014

A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects.

A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: January 18, 2014

A deletion including exon 2 of the TSHR gene is associated with thyroid dysgenesis and severe congenital hypothyroidism.

A deletion including exon 2 of the TSHR gene is associated with thyroid dysgenesis and severe congenital hypothyroidism.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: January 10, 2014

A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism.

A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 31, 2013

A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect.

A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: May 21, 2013

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Last Updated: 09/26/2026