Nussbaum RL - Search Results

1

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: nussbaum rl. Dev Biol. 2001 Dec 15;240(2):641-53. doi: 10.1006/dbio.2001.0476. Dev Biol. 2001. PMID: 11784089 Free article.

2

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

Bernard DJ, Nussbaum RL. Bernard DJ, et al. Among authors: nussbaum rl. 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

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. Among authors: nussbaum rl. Biol Reprod. 2002 May;66(5):1522-30. doi: 10.1095/biolreprod66.5.1522. Biol Reprod. 2002. PMID: 11967219

4

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. Among authors: nussbaum rl. Mamm Genome. 2002 Mar;13(3):169-72. doi: 10.1007/BF02684023. Mamm Genome. 2002. PMID: 11919689 No abstract available.

5

Localization of the 75-kDa inositol polyphosphate-5-phosphatase (INPP5B) to human chromosome band 1p34.

Jänne PA, Dutra AS, Dracopoli NC, Charnas LR, Puck JM, Nussbaum RL. Jänne PA, et al. Among authors: nussbaum rl. Cytogenet Cell Genet. 1994;66(3):164-6. doi: 10.1159/000133691. Cytogenet Cell Genet. 1994. PMID: 8125013

6

Mapping of the 75-kDa inositol polyphosphate-5-phosphatase (Inpp5b) to distal mouse chromosome 4 and its exclusion as a candidate gene for dysgenetic lens.

Jänne PA, Rochelle JM, Martin-DeLeon PA, Stambolian D, Seldin MF, Nussbaum RL. Jänne PA, et al. Among authors: nussbaum rl. Genomics. 1995 Jul 20;28(2):280-5. doi: 10.1006/geno.1995.1142. Genomics. 1995. PMID: 8530037 Free article.

7

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: nussbaum rl. J Clin Invest. 1998 May 15;101(10):2042-53. doi: 10.1172/JCI2414. J Clin Invest. 1998. PMID: 9593760 Free PMC article.

8

Physical mapping and genomic structure of the Lowe syndrome gene OCRL1.

Nussbaum RL, Orrison BM, Jänne PA, Charnas L, Chinault AC. Nussbaum RL, et al. Hum Genet. 1997 Feb;99(2):145-50. doi: 10.1007/s004390050329. Hum Genet. 1997. PMID: 9048911

9

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: nussbaum rl. Am J Hum Genet. 1997 Jun;60(6):1384-8. doi: 10.1086/515471. Am J Hum Genet. 1997. PMID: 9199559 Free PMC article.

10

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: nussbaum rl. 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.

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