Morison IM - Search Results

1

Wilms tumor in patients with osteopathia striata with cranial sclerosis.

Bach A, Mi J, Hunter M, Halliday BJ, García-Miñaúr S, Sperotto F, Trevisson E, Markie D, Morison IM, Shinawi M, Willis DN, Robertson SP. Bach A, et al. Among authors: morison im. Eur J Hum Genet. 2021 Mar;29(3):396-401. doi: 10.1038/s41431-020-00718-4. Epub 2020 Sep 2. Eur J Hum Genet. 2021. PMID: 32879452 Free PMC article.

2

A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.

Heathcott RW, Morison IM, Gubler MC, Corbett R, Reeve AE. Heathcott RW, et al. Among authors: morison im. Hum Mutat. 2002 Apr;19(4):462. doi: 10.1002/humu.9031. Hum Mutat. 2002. PMID: 11933209 Review.

3

Germline mutations and somatic inactivation of TRIM28 in Wilms tumour.

Halliday BJ, Fukuzawa R, Markie DM, Grundy RG, Ludgate JL, Black MA, Skeen JE, Weeks RJ, Catchpoole DR, Roberts AGK, Reeve AE, Morison IM. Halliday BJ, et al. Among authors: morison im. PLoS Genet. 2018 Jun 18;14(6):e1007399. doi: 10.1371/journal.pgen.1007399. eCollection 2018 Jun. PLoS Genet. 2018. PMID: 29912901 Free PMC article.

4

Tuberous sclerosis complex: a complex case.

Powell RM, Pattison S, Moravec JC, Bhat B, Guirguis N, Markie D, Jones GT, Copedo J, Print CG, Morison IM, Gavryushkin A, Gray B, Wyeth LJ, Eccles MR, Macaulay EC. Powell RM, et al. Among authors: morison im. Cold Spring Harb Mol Case Stud. 2022 Apr 28;8(3):a006182. doi: 10.1101/mcs.a006182. Print 2022 Apr. Cold Spring Harb Mol Case Stud. 2022. PMID: 35483879 Free PMC article.

5

Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism.

Ogawa O, Becroft DM, Morison IM, Eccles MR, Skeen JE, Mauger DC, Reeve AE. Ogawa O, et al. Among authors: morison im. Nat Genet. 1993 Dec;5(4):408-12. doi: 10.1038/ng1293-408. Nat Genet. 1993. PMID: 8298652

6

Somatic overgrowth associated with overexpression of insulin-like growth factor II.

Morison IM, Becroft DM, Taniguchi T, Woods CG, Reeve AE. Morison IM, et al. Nat Med. 1996 Mar;2(3):311-6. doi: 10.1038/nm0396-311. Nat Med. 1996. PMID: 8612230

7

Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-beckwith syndrome.

Itoh N, Becroft DM, Reeve AE, Morison IM. Itoh N, et al. Among authors: morison im. Am J Med Genet. 2000 May 15;92(2):111-6. Am J Med Genet. 2000. PMID: 10797434

8

Canonical WNT signalling determines lineage specificity in Wilms tumour.

Fukuzawa R, Anaka MR, Weeks RJ, Morison IM, Reeve AE. Fukuzawa R, et al. Among authors: morison im. Oncogene. 2009 Feb 26;28(8):1063-75. doi: 10.1038/onc.2008.455. Epub 2009 Jan 12. Oncogene. 2009. PMID: 19137020

9

Global demethylation in loss of imprinting subtype of Wilms tumor.

Ludgate JL, Le Mée G, Fukuzawa R, Rodger EJ, Weeks RJ, Reeve AE, Morison IM. Ludgate JL, et al. Among authors: morison im. Genes Chromosomes Cancer. 2013 Feb;52(2):174-84. doi: 10.1002/gcc.22017. Epub 2012 Oct 17. Genes Chromosomes Cancer. 2013. PMID: 23074036

10

Altered specificity of IGF2 promoter imprinting during fetal development and onset of Wilms tumour.

Taniguchi T, Schofield AE, Scarlett JL, Morison IM, Sullivan MJ, Reeve AE. Taniguchi T, et al. Among authors: morison im. Oncogene. 1995 Aug 17;11(4):751-6. Oncogene. 1995. PMID: 7651739

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

95 results

Search Page