ISSN 1470-3947 (print) | ISSN 1479-6848 (online)

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Showing page 1 of results 1 - 10 of about 10 pages

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The calcilytic SHP635 rectifies hypocalcaemia and reduced parathyroid hormone concentrations in a mouse model for autosomal dominant hypocalcaemia type 1 (ADH1)
Fadil Hannan; Valerie Babinsky; Caroline Gorvin; Tertius Hough; Elizabeth Joynson; Michelle Stewart; Sara Wells; Roger Cox; Edwa
http://www.endocrine-abstracts.org/ea/0044/ea0044p44.htm
Published: 2016-10-14

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Localisation of a renal calcification locus to a 5 Mbp-region on mouse chromosome 11D-E2
Bushra Ahmad; Nellie Loh; Anita Reed; Michael Stechman; Michelle Stewart; Terry Hacker; Sara Wells; Tertius Hough; Liz Bentley;
http://www.endocrine-abstracts.org/ea/0013/ea0013p12.htm
Published: 2007-03-01

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Mapping of a renal calcification locus to a 5-megabase region on mouse chromosome 17B1/B2
Michael Stechman; Nellie Loh; Anita Reed; Bushra Ahmad; Michelle Stewart; Terry Hacker; Sara Wells; Tertius Hough; Liz Bentley;
http://www.endocrine-abstracts.org/ea/0013/ea0013p4.htm
Published: 2007-03-01

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Studies of Nuf mice with an activating calcium-sensing receptor (CaSR) mutation demonstrate the CaSR to regulate pancreatic beta-cell mass and glucose homeostasis
Valerie N Babinsky; Fadil M Hannan; M Andrew Nesbit; Alison Hough; Michelle Stewart; Elizabeth Joynson; Tertius A Hough; Liz Ben
http://www.endocrine-abstracts.org/ea/0038/ea0038p186.htm
Published: 2015-10-12

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Mice with a gain-of function G[alpha]<SUB>11</SUB> mutation have autosomal dominant hypocalcaemia, but not impaired glucose metabolism | SFEBES2019
Anna Gluck; Kate Lines; Caroline Gorvin; Valerie Babinsky; Sian Piret; Stefan Sarbu; Michelle Stewart; Liz Bentley; Sara Wells;
https://www.endocrine-abstracts.org/ea/0065/ea0065op3.4
Published: 2019-11-06

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Mice with a gain-of function G[alpha]<SUB>11</SUB> mutation have autosomal dominant hypocalcaemia, but not impaired glucose metabolism | SFEBES2019
Anna Gluck; Kate Lines; Caroline Gorvin; Valerie Babinsky; Sian Piret; Stefan Sarbu; Michelle Stewart; Liz Bentley; Sara Wells;
https://www.endocrine-abstracts.org/ea/0065/ea0065op3.4.htm
Published: 2019-11-06

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A mouse model generated by CRISPR-Cas9 with a frameshift mutation in the nuclear factor 1/X (<em>NFIX</em>) gene has phenotypic features reported in Marshall-Smith Syndrome (MSS) patients | SFEBES2019
Kreepa Kooblall; Mark Stevenson; Michelle Stewart; Zsombor Szoke-Kovacs; Tertius Hough; Houfu Leng; Nicole Horwood; Tonia Vincen
https://www.endocrine-abstracts.org/ea/0065/ea0065oc3.1
Published: 2019-11-06

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A mouse model generated by CRISPR-Cas9 with a frameshift mutation in the nuclear factor 1/X (<em>NFIX</em>) gene has phenotypic features reported in Marshall-Smith Syndrome (MSS) patients | SFEBES2019
Kreepa Kooblall; Mark Stevenson; Michelle Stewart; Zsombor Szoke-Kovacs; Tertius Hough; Houfu Leng; Nicole Horwood; Tonia Vincen
https://www.endocrine-abstracts.org/ea/0065/ea0065oc3.1.htm
Published: 2019-11-06

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Mice harbouring a germline heterozygous AP2S1 mutation, Arg15Leu, are a model for familial hypocalciuric hypercalcaemia type 3 (FHH3) | SFEBES2019
Fadil Hannan; Victoria Stokes; Caroline Gorvin; Mark Stevenson; Tertius Hough; Michelle Stewart; Sara Wells; Lydia Teboul; Rajes
https://www.endocrine-abstracts.org/ea/0065/ea0065ec1.4
Published: 2019-11-06

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Mice harbouring a germline heterozygous AP2S1 mutation, Arg15Leu, are a model for familial hypocalciuric hypercalcaemia type 3 (FHH3) | SFEBES2019
Fadil Hannan; Victoria Stokes; Caroline Gorvin; Mark Stevenson; Tertius Hough; Michelle Stewart; Sara Wells; Lydia Teboul; Rajes
https://www.endocrine-abstracts.org/ea/0065/ea0065ec1.4.htm
Published: 2019-11-06

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