Bernard D - Search Results

1

Functional overlap between murine Inpp5b and Ocrl1 may explain why deficiency of the murine ortholog for OCRL1 does not cause Lowe syndrome in mice.

Jänne PA, Suchy SF, Bernard D, MacDonald M, Crawley J, Grinberg A, Wynshaw-Boris A, Westphal H, Nussbaum RL. Jänne PA, et al. Among authors: bernard d. J Clin Invest. 1998 May 15;101(10):2042-53. doi: 10.1172/JCI2414. J Clin Invest. 1998. PMID: 9593760 Free PMC article.

2

X-inactivation analysis of embryonic lethality in Ocrl wt/-; Inpp5b-/- mice.

Bernard DJ, Nussbaum RL. Bernard DJ, et al. Mamm Genome. 2010 Apr;21(3-4):186-94. doi: 10.1007/s00335-010-9255-9. Epub 2010 Feb 27. Mamm Genome. 2010. PMID: 20195868 Free PMC article.

3

Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome.

Lin T, Orrison BM, Leahey AM, Suchy SF, Bernard DJ, Lewis RA, Nussbaum RL. Lin T, et al. Among authors: bernard dj. Am J Hum Genet. 1997 Jun;60(6):1384-8. doi: 10.1086/515471. Am J Hum Genet. 1997. PMID: 9199559 Free PMC article.

4

Disrupted sperm function and fertilin beta processing in mice deficient in the inositol polyphosphate 5-phosphatase Inpp5b.

Hellsten E, Evans JP, Bernard DJ, Jänne PA, Nussbaum RL. Hellsten E, et al. Among authors: bernard dj. Dev Biol. 2001 Dec 15;240(2):641-53. doi: 10.1006/dbio.2001.0476. Dev Biol. 2001. PMID: 11784089 Free article.

5

Sertoli cell vacuolization and abnormal germ cell adhesion in mice deficient in an inositol polyphosphate 5-phosphatase.

Hellsten E, Bernard DJ, Owens JW, Eckhaus M, Suchy SF, Nussbaum RL. Hellsten E, et al. Biol Reprod. 2002 May;66(5):1522-30. doi: 10.1095/biolreprod66.5.1522. Biol Reprod. 2002. PMID: 11967219

6

Proliferative defect and embryonic lethality in mice homozygous for a deletion in the p110alpha subunit of phosphoinositide 3-kinase.

Bi L, Okabe I, Bernard DJ, Wynshaw-Boris A, Nussbaum RL. Bi L, et al. Among authors: bernard dj. J Biol Chem. 1999 Apr 16;274(16):10963-8. doi: 10.1074/jbc.274.16.10963. J Biol Chem. 1999. PMID: 10196176 Free article.

7

High resolution MRI reveals global changes in brains of Cln3 mutant mice.

Greene ND, Lythgoe MF, Thomas DL, Nussbaum RL, Bernard DJ, Mitchison HM. Greene ND, et al. Among authors: bernard dj. Eur J Paediatr Neurol. 2001;5 Suppl A:103-7. doi: 10.1053/ejpn.2000.0444. Eur J Paediatr Neurol. 2001. PMID: 11588978

8

Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected].

Mitchison HM, Bernard DJ, Greene ND, Cooper JD, Junaid MA, Pullarkat RK, de Vos N, Breuning MH, Owens JW, Mobley WC, Gardiner RM, Lake BD, Taschner PE, Nussbaum RL. Mitchison HM, et al. Among authors: bernard dj. Neurobiol Dis. 1999 Oct;6(5):321-34. doi: 10.1006/nbdi.1999.0267. Neurobiol Dis. 1999. PMID: 10527801

9

Early embryonic lethality in mice deficient in the p110beta catalytic subunit of PI 3-kinase.

Bi L, Okabe I, Bernard DJ, Nussbaum RL. Bi L, et al. Mamm Genome. 2002 Mar;13(3):169-72. doi: 10.1007/BF02684023. Mamm Genome. 2002. PMID: 11919689 No abstract available.

10

Retinal pathology and function in a Cln3 knockout mouse model of juvenile Neuronal Ceroid Lipofuscinosis (batten disease).

Seigel GM, Lotery A, Kummer A, Bernard DJ, Greene ND, Turmaine M, Derksen T, Nussbaum RL, Davidson B, Wagner J, Mitchison HM. Seigel GM, et al. Among authors: bernard dj. Mol Cell Neurosci. 2002 Apr;19(4):515-27. doi: 10.1006/mcne.2001.1099. Mol Cell Neurosci. 2002. PMID: 11988019

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