Erik Schoenmakers and Mutation - Free people check

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A Mutation in the Thyroid Hormone Receptor Alpha Gene

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by E Bochukova · · Cited by 368 — Elena Bochukova, D.Phil.,; Nadia Schoenmakers, M.B.,; Maura Agostini, Ph.D.,; Erik Schoenmakers, Ph.D.,; Odelia Rajanayagam, B.Sc., ... › doi › full › nejmoa

Nadia Schoenmakers - Typeset.io

typeset.io

978 results — A mutation in the thyroid hormone receptor alpha gene. Elena G. Bochukova 1, Nadia Schoenmakers 2, Maura Agostini, Erik Schoenmakers +19 more ... › authors

Selenium: Its Molecular Biology and Role in Human Health

books.google.cz

Erik Schoenmakers, Nadia Schoenmakers, and Krishna Chatterjee Abstract Human mutations have been described in three genes implicated in the selenocysteine ...

Resistance to thyroid hormone caused by a mutation in thyroid hormone...

www.sciencedirect.com

Carla Moran*, Maura Agostini*, W Edward Visser, Erik Schoenmakers, Nadia Schoenmakers, Amaka C Offiah, Ken Poole, Odelia ...

Homozygous loss-of-function mutations in SLC26A7 cause ...

core.ac.uk

by H Cangul · Cited by 40 — Hakan Cangul,1 Xiao-Hui Liao,2 Erik Schoenmakers,3 Jukka Kero,4,5 Sharon Barone,6. Panudda Srichomkwun,2 Hideyuki Iwayama,2 Eva G. Serra,7 Halil Saglam, › download › pdf

A Mutation in the Thyroid Hormone Receptor Alpha Gene

research.amanote.com

A Mutation in the Thyroid Hormone Receptor Alpha Gene by Elena Bochukova, Nadia Schoenmakers, Maura Agostini, Erik Schoenmakers, Odelia Rajanayagam, › publication › a-mutation...

Homozygous loss-of-function mutations in SLC26A7 cause ...

research.utu.fi

List of Authors: Hakan Cangul, Xiao-Hui Liao, Erik Schoenmakers, Jukka Kero, Sharon Barone, Panudda Srichomkwun, Hideyuki Iwayama, Eva G. Serra, ... › portal › detail › Publication

All web results to the name "Erik Schoenmakers"

Homozygous loss-of-function mutations in UTUPub

www.utupub.fi

Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism. Hakan Cangul, Xiao-Hui Liao, Erik Schoenmakers, Jukka Kero, ... › handle

Mutation in human selenocysteine HAL Sorbonne Université

hal.sorbonne-universite.fr

by E Schoenmakers · · Cited by 69 — Erik Schoenmakers 1 Bradley Carlson 2 Maura Agostini 1 Carla Moran 1 Odelia Rajanayagam 1 Elena Bochukova 1 Ryuta Tobe 2 Rachel Peat 3 Evelien Gevers › hal

Mutation in human selenocysteine transfer RNA selectively ...

go.gale.com

by E Schoenmakers · · Cited by 69 — Gale OneFile includes Mutation in human selenocysteine transfer RNA selective by Erik Schoenmakers, Bradley Carlson, Mau. Click to explore. › i.do

Mutations in thyroid hormone receptor α1 cause premature ...

www.biorxiv.org

Jan 26, — Teresa G Krieger, Carla M Moran, Alberto Frangini, W Edward Visser, Erik Schoenmakers, Francesco Muntoni, Chris Clark, David Gadian, ... › content

Erik Schoenmakers

endo.confex.com

Erik Schoenmakers. University of Cambridge Institute of Metabolic Science Papers: OR29-1 Resistance to Thyroid Hormone Mediated By a Missense Mutation ...

JCI - Mutations in the selenocysteine insertion sequence–binding...

www.jci.org

Erik Schoenmakers ... Mark Gurnell, Krishna Chatterjee Published December 1, Citation Information: J Clin Invest ;120(12): doi: JCI

Resistance to thyroid hormone caused by a mutation in thyroid hormone...

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Carla Moran, Maura Agostini, W Edward Visser, Erik Schoenmakers, Nadia Schoenmakers, Amaka C Offiah, Ken Poole, Odelia Rajanayagam, Greta Lyons, ...

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