Stewart M - Search Results

1

An Improved Method for Growing Primary Neurons on Electron Microscopy Grids Co-Cultured with Astrocytes.

Kumar I, Paudyal A, Kádková A, Stewart M, Sørensen JB, Radecke J. Kumar I, et al. Among authors: stewart m. Int J Mol Sci. 2023 Oct 14;24(20):15191. doi: 10.3390/ijms242015191. Int J Mol Sci. 2023. PMID: 37894872 Free PMC article.

2

Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway.

Patterson VL, Damrau C, Paudyal A, Reeve B, Grimes DT, Stewart ME, Williams DJ, Siggers P, Greenfield A, Murdoch JN. Patterson VL, et al. Hum Mol Genet. 2009 May 15;18(10):1719-39. doi: 10.1093/hmg/ddp075. Epub 2009 Feb 17. Hum Mol Genet. 2009. PMID: 19223390 Free PMC article.

3

Gα₁₁ mutation in mice causes hypocalcemia rectifiable by calcilytic therapy.

Gorvin CM, Hannan FM, Howles SA, Babinsky VN, Piret SE, Rogers A, Freidin AJ, Stewart M, Paudyal A, Hough TA, Nesbit MA, Wells S, Vincent TL, Brown SD, Cox RD, Thakker RV. Gorvin CM, et al. Among authors: stewart m. JCI Insight. 2017 Feb 9;2(3):e91103. doi: 10.1172/jci.insight.91103. JCI Insight. 2017. PMID: 28194447 Free PMC article.

4

Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutation.

Howles SA, Hannan FM, Gorvin CM, Piret SE, Paudyal A, Stewart M, Hough TA, Nesbit MA, Wells S, Brown SD, Cox RD, Thakker RV. Howles SA, et al. Among authors: stewart m. JCI Insight. 2017 Oct 19;2(20):e96540. doi: 10.1172/jci.insight.96540. JCI Insight. 2017. PMID: 29046478 Free PMC article.

5

N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss-of-Function Mice.

Gorvin CM, Rogers A, Stewart M, Paudyal A, Hough TA, Teboul L, Wells S, Brown SD, Cox RD, Thakker RV. Gorvin CM, et al. Among authors: stewart m. JBMR Plus. 2017 May 2;1(1):3-15. doi: 10.1002/jbm4.10001. JBMR Plus. 2017. PMID: 29479578 Free PMC article.

6

Mylk3 null C57BL/6N mice develop cardiomyopathy, whereas Nnt null C57BL/6J mice do not.

Williams JL, Paudyal A, Awad S, Nicholson J, Grzesik D, Botta J, Meimaridou E, Maharaj AV, Stewart M, Tinker A, Cox RD, Metherell LA. Williams JL, et al. Among authors: stewart m. Life Sci Alliance. 2020 Mar 25;3(4):e201900593. doi: 10.26508/lsa.201900593. Print 2020 Apr. Life Sci Alliance. 2020. PMID: 32213617 Free PMC article.

7

Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2.

Hannan FM, Stevenson M, Bayliss AL, Stokes VJ, Stewart M, Kooblall KG, Gorvin CM, Codner G, Teboul L, Wells S, Thakker RV. Hannan FM, et al. Among authors: stewart m. Hum Mol Genet. 2021 May 29;30(10):880-892. doi: 10.1093/hmg/ddab076. Hum Mol Genet. 2021. PMID: 33729479 Free PMC article.

8

Mutant Tbl1x male mice have a short life span and do not breed: unexpected findings.

Hu Y, Codner GF, Stewart M, La Fleur SE, van Trotsenburg PAS, Fliers E, Hennekam RC, Boelen A. Hu Y, et al. Among authors: stewart m. J Mol Endocrinol. 2024 Mar 22;73(1):e230116. doi: 10.1530/JME-23-0116. Print 2024 Jul 1. J Mol Endocrinol. 2024. PMID: 38381448

9

The effects of microchipping C57BL/6N mice on standard phenotyping tests.

Bains RS, Cater HL, Stewart M, Scudamore CL, Wells SE. Bains RS, et al. Among authors: stewart m. F1000Res. 2020 Jan 14;9:20. doi: 10.12688/f1000research.21633.2. eCollection 2020. F1000Res. 2020. PMID: 32399198 Free PMC article.

10

An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutation.

Hu Y, Lauffer P, Stewart M, Codner G, Mayerl S, Heuer H, Ng L, Forrest D, van Trotsenburg P, Jongejan A, Fliers E, Hennekam R, Boelen A. Hu Y, et al. Among authors: stewart m. Hum Mol Genet. 2022 Aug 25;31(17):2951-2963. doi: 10.1093/hmg/ddac086. Hum Mol Genet. 2022. PMID: 35416977 Free PMC article.

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