Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 63

1.

Impaired neurogenesis and associated gliosis in mouse brain with PEX13 deficiency.

Rahim RS, St John JA, Crane DI, Meedeniya ACB.

Mol Cell Neurosci. 2018 Apr;88:16-32. doi: 10.1016/j.mcn.2017.11.015. Epub 2017 Dec 2.

PMID:
29187321
2.

Peroxisomal protein PEX13 functions in selective autophagy.

Lee MY, Sumpter R Jr, Zou Z, Sirasanagandla S, Wei Y, Mishra P, Rosewich H, Crane DI, Levine B.

EMBO Rep. 2017 Jan;18(1):48-60. doi: 10.15252/embr.201642443. Epub 2016 Nov 8.

3.

Mitochondrial changes and oxidative stress in a mouse model of Zellweger syndrome neuropathogenesis.

Rahim RS, Chen M, Nourse CC, Meedeniya AC, Crane DI.

Neuroscience. 2016 Oct 15;334:201-213. doi: 10.1016/j.neuroscience.2016.08.001. Epub 2016 Aug 8.

PMID:
27514574
4.

Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic Paraplegia.

Wali G, Sutharsan R, Fan Y, Stewart R, Tello Velasquez J, Sue CM, Crane DI, Mackay-Sim A.

Sci Rep. 2016 May 27;6:27004. doi: 10.1038/srep27004.

5.

A new disaster victim identification management strategy targeting "near identification-threshold" cases: Experiences from the Boxing Day tsunami.

Wright K, Mundorff A, Chaseling J, Forrest A, Maguire C, Crane DI.

Forensic Sci Int. 2015 May;250:91-7. doi: 10.1016/j.forsciint.2015.03.007. Epub 2015 Mar 18.

PMID:
25828381
6.

Central serotonergic neuron deficiency in a mouse model of Zellweger syndrome.

Rahim RS, Meedeniya AC, Crane DI.

Neuroscience. 2014 Aug 22;274:229-41. doi: 10.1016/j.neuroscience.2014.05.034. Epub 2014 May 29.

PMID:
24881576
7.

Low dose tubulin-binding drugs rescue peroxisome trafficking deficit in patient-derived stem cells in Hereditary Spastic Paraplegia.

Fan Y, Wali G, Sutharsan R, Bellette B, Crane DI, Sue CM, Mackay-Sim A.

Biol Open. 2014 May 23;3(6):494-502. doi: 10.1242/bio.20147641.

8.

Revisiting the neuropathogenesis of Zellweger syndrome.

Crane DI.

Neurochem Int. 2014 Apr;69:1-8. doi: 10.1016/j.neuint.2014.02.007. Epub 2014 Mar 6. Review.

PMID:
24607700
9.

Excess iron modulates endoplasmic reticulum stress-associated pathways in a mouse model of alcohol and high-fat diet-induced liver injury.

Tan TC, Crawford DH, Jaskowski LA, Subramaniam VN, Clouston AD, Crane DI, Bridle KR, Anderson GJ, Fletcher LM.

Lab Invest. 2013 Dec;93(12):1295-312. doi: 10.1038/labinvest.2013.121. Epub 2013 Oct 14.

10.

The biogenesis protein PEX14 is an optimal marker for the identification and localization of peroxisomes in different cell types, tissues, and species in morphological studies.

Grant P, Ahlemeyer B, Karnati S, Berg T, Stelzig I, Nenicu A, Kuchelmeister K, Crane DI, Baumgart-Vogt E.

Histochem Cell Biol. 2013 Oct;140(4):423-42.

PMID:
23959168
11.

RhoA regulation of cardiomyocyte differentiation.

Kaarbø M, Crane DI, Murrell WG.

ScientificWorldJournal. 2013 Jun 27;2013:491546. doi: 10.1155/2013/491546. Print 2013.

12.

Glucocorticoids alleviate intestinal ER stress by enhancing protein folding and degradation of misfolded proteins.

Das I, Png CW, Oancea I, Hasnain SZ, Lourie R, Proctor M, Eri RD, Sheng Y, Crane DI, Florin TH, McGuckin MA.

J Exp Med. 2013 Jun 3;210(6):1201-16. doi: 10.1084/jem.20121268. Epub 2013 May 6.

13.

PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress.

Müller CC, Nguyen TH, Ahlemeyer B, Meshram M, Santrampurwala N, Cao S, Sharp P, Fietz PB, Baumgart-Vogt E, Crane DI.

Dis Model Mech. 2011 Jan;4(1):104-19. doi: 10.1242/dmm.004622. Epub 2010 Oct 19.

14.

alpha-Synuclein abnormalities in mouse models of peroxisome biogenesis disorders.

Yakunin E, Moser A, Loeb V, Saada A, Faust P, Crane DI, Baes M, Sharon R.

J Neurosci Res. 2010 Mar;88(4):866-76. doi: 10.1002/jnr.22246.

15.

Quantitative genotyping of mouse brain-specific PEX13 gene disruption by real-time PCR.

Müller CC, Nourse JP, Nguyen TH, Crane DI.

J Neurosci Methods. 2009 Jun 30;181(1):73-81. doi: 10.1016/j.jneumeth.2009.04.025. Epub 2009 May 5.

PMID:
19422853
16.

Fuzzy scaling analysis of a mouse mutant with brain morphological changes.

Pham TD, Müller CC, Crane DI.

IEEE Trans Inf Technol Biomed. 2009 Jul;13(4):629-35. doi: 10.1109/TITB.2009.2019638. Epub 2009 Apr 14.

PMID:
19369166
17.

A region analysis approach for segmenting neural-cell images.

Yu D, Pham TD, Crane DI.

Conf Proc IEEE Eng Med Biol Soc. 2007;2007:5529-32.

PMID:
18003264
18.

Segmentation of cultured neurons using logical analysis of grey and distance difference.

Yu D, Pham TD, Yan H, Zhang B, Crane DI.

J Neurosci Methods. 2007 Oct 15;166(1):125-37. Epub 2007 Jul 7.

PMID:
17689665
19.

Segmentation of neuronal-cell images from stained fields and monomodal histograms.

Pham TD, Crane DI.

Conf Proc IEEE Eng Med Biol Soc. 2005;6:6289-92.

PMID:
17281705
20.

Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance.

Nguyen T, Bjorkman J, Paton BC, Crane DI.

J Cell Sci. 2006 Feb 15;119(Pt 4):636-45. Epub 2006 Jan 31.

21.

Novel PEX1 coding mutations and 5' UTR regulatory polymorphisms.

Maxwell MA, Leane PB, Paton BC, Crane DI.

Hum Mutat. 2005 Sep;26(3):279.

PMID:
16088892
22.

PEX1 mutations in the Zellweger spectrum of the peroxisome biogenesis disorders.

Crane DI, Maxwell MA, Paton BC.

Hum Mutat. 2005 Sep;26(3):167-75. Review.

PMID:
16086329
23.

Extraction of fluorescent cell puncta by adaptive fuzzy segmentation.

Pham TD, Crane DI, Tran TH, Nguyen TH.

Bioinformatics. 2004 Sep 22;20(14):2189-96. Epub 2004 Apr 1.

PMID:
15059837
24.

Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype.

Maxwell M, Bjorkman J, Nguyen T, Sharp P, Finnie J, Paterson C, Tonks I, Paton BC, Kay GF, Crane DI.

Mol Cell Biol. 2003 Aug;23(16):5947-57.

25.
26.

Novel PEX1 mutations and genotype-phenotype correlations in Australasian peroxisome biogenesis disorder patients.

Maxwell MA, Allen T, Solly PB, Svingen T, Paton BC, Crane DI.

Hum Mutat. 2002 Nov;20(5):342-51.

PMID:
12402331
27.

Conditional inactivation of the peroxisome biogenesis Pex13 gene by Cre-loxP excision.

Bjorkman J, Tonks I, Maxwell MA, Paterson C, Kay GF, Crane DI.

Genesis. 2002 Feb;32(2):179-80. No abstract available.

PMID:
11857814
29.

Characterisation of a cDNA encoding chick eukaryotic translation initiation factor-2 beta.

Sneesby KJ, Crane DI, Murrell WG.

DNA Seq. 2001 Jul;12(1):59-65.

PMID:
11697145
30.

GABA(A) receptor alpha-subunit proteins in human chronic alcoholics.

Lewohl JM, Huygens F, Crane DI, Dodd PR.

J Neurochem. 2001 Aug;78(3):424-34.

31.

Isolation and characterisation of a chick cDNA encoding the RNA polymerase common subunit RPB6.

Kaarbo M, Crane DI, Murrell WG.

DNA Seq. 2000;11(1-2):155-62.

PMID:
10902924
32.

Placental growth hormone (GH), GH-binding protein, and insulin-like growth factor axis in normal, growth-retarded, and diabetic pregnancies: correlations with fetal growth.

McIntyre HD, Serek R, Crane DI, Veveris-Lowe T, Parry A, Johnson S, Leung KC, Ho KK, Bougoussa M, Hennen G, Igout A, Chan FY, Cowley D, Cotterill A, Barnard R.

J Clin Endocrinol Metab. 2000 Mar;85(3):1143-50.

33.
34.

Localization of a portion of extranuclear ATM to peroxisomes.

Watters D, Kedar P, Spring K, Bjorkman J, Chen P, Gatei M, Birrell G, Garrone B, Srinivasa P, Crane DI, Lavin MF.

J Biol Chem. 1999 Nov 26;274(48):34277-82.

35.

A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotype.

Maxwell MA, Nelson PV, Chin SJ, Paton BC, Carey WF, Crane DI.

Hum Genet. 1999 Jul-Aug;105(1-2):38-44.

PMID:
10480353
36.

PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.

Liu Y, Björkman J, Urquhart A, Wanders RJ, Crane DI, Gould SJ.

Am J Hum Genet. 1999 Sep;65(3):621-34.

37.

Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene.

Björkman J, Stetten G, Moore CS, Gould SJ, Crane DI.

Genomics. 1998 Dec 15;54(3):521-8.

PMID:
9878256
38.
39.

Zolpidem binding sites on the GABA(A) receptor in brain from human cirrhotic and non-cirrhotic alcoholics.

Lewohl JM, Crane DI, Dodd PR.

Eur J Pharmacol. 1997 May 20;326(2-3):265-72.

PMID:
9196280
40.

Expression of the alpha 1, alpha 2 and alpha 3 isoforms of the GABAA receptor in human alcoholic brain.

Lewohl JM, Crane DI, Dodd PR.

Brain Res. 1997 Mar 14;751(1):102-12.

PMID:
9098573
41.

Alcohol, alcoholic brain damage, and GABAA receptor isoform gene expression.

Lewohl JM, Crane DI, Dodd PR.

Neurochem Int. 1996 Dec;29(6):677-84.

PMID:
9113136
42.

Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor.

Gould SJ, Kalish JE, Morrell JC, Bjorkman J, Urquhart AJ, Crane DI.

J Cell Biol. 1996 Oct;135(1):85-95.

43.

A unified nomenclature for peroxisome biogenesis factors.

Distel B, Erdmann R, Gould SJ, Blobel G, Crane DI, Cregg JM, Dodt G, Fujiki Y, Goodman JM, Just WW, Kiel JA, Kunau WH, Lazarow PB, Mannaerts GP, Moser HW, Osumi T, Rachubinski RA, Roscher A, Subramani S, Tabak HF, Tsukamoto T, Valle D, van der Klei I, van Veldhoven PP, Veenhuis M.

J Cell Biol. 1996 Oct;135(1):1-3. Review. No abstract available.

44.

The neurochemical pathology of thiamine deficiency: GABAA and glutamateNMDA receptor binding sites in a goat model.

Dodd PR, Thomas GJ, McCloskey A, Crane DI, Smith ID.

Metab Brain Dis. 1996 Mar;11(1):39-54.

PMID:
8815389
45.
47.

Chromatin structure and the expression of cardiac genes.

Murrell WG, Masters CJ, Willis RJ, Crane DI.

Mech Ageing Dev. 1995 Jul 28;82(1):1-17.

PMID:
7475353
48.

On the role of the peroxisome in ontogeny, ageing and degenerative disease.

Masters CJ, Crane DI.

Mech Ageing Dev. 1995 May 12;80(2):69-83. Review.

PMID:
7564565
49.

On the ontogeny of cardiac gene transcripts.

Murrell WG, Masters CJ, Willis RJ, Crane DI.

Mech Ageing Dev. 1994 Dec 16;77(2):109-26.

PMID:
7745990

Supplemental Content

Loading ...
Support Center