O'Lague P - Search Results

1

ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome.

Curry CJ, O'Lague P, Tsai J, Hutchison HT, Jaspers NG, Wara D, Gatti RA. Curry CJ, et al. Among authors: o lague p. Am J Hum Genet. 1989 Aug;45(2):270-5. Am J Hum Genet. 1989. PMID: 2491181 Free PMC article.

2

Mild autosomal dominant hypophosphatasia: in utero presentation in two families.

Moore CA, Curry CJ, Henthorn PS, Smith JA, Smith JC, O'Lague P, Coburn SP, Weaver DD, Whyte MP. Moore CA, et al. Among authors: o lague p. Am J Med Genet. 1999 Oct 29;86(5):410-5. doi: 10.1002/(sici)1096-8628(19991029)86:5<410::aid-ajmg3>3.0.co;2-0. Am J Med Genet. 1999. PMID: 10508980

3

Elucidation of the cytogenetic abnormality in a 4p- "phenocopy".

Curry CJ, Ying KL, O'Lague P, Tsai J. Curry CJ, et al. Birth Defects Orig Artic Ser. 1982;18(3B):275-86. Birth Defects Orig Artic Ser. 1982. PMID: 7139110 No abstract available.

4

Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random association.

Verloes A, Curry C, Jamar M, Herens C, O'Lague P, Marks J, Sarda P, Blanchet P. Verloes A, et al. Among authors: o lague p. J Med Genet. 1998 Nov;35(11):943-7. doi: 10.1136/jmg.35.11.943. J Med Genet. 1998. PMID: 9832043 Free PMC article.

5

Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.

Curry CJ, Magenis RE, Brown M, Lanman JT Jr, Tsai J, O'Lague P, Goodfellow P, Mohandas T, Bergner EA, Shapiro LJ. Curry CJ, et al. Among authors: o lague p. N Engl J Med. 1984 Oct 18;311(16):1010-5. doi: 10.1056/NEJM198410183111603. N Engl J Med. 1984. PMID: 6482910

6

De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing.

Strom SP, Lozano R, Lee H, Dorrani N, Mann J, O'Lague PF, Mans N, Deignan JL, Vilain E, Nelson SF, Grody WW, Quintero-Rivera F. Strom SP, et al. Among authors: o lague pf. BMC Med Genet. 2014 May 1;15:49. doi: 10.1186/1471-2350-15-49. BMC Med Genet. 2014. PMID: 24886118 Free PMC article.

7

Mechanical force generation by G proteins.

Kosztin I, Bruinsma R, O'Lague P, Schulten K. Kosztin I, et al. Among authors: o lague p. Proc Natl Acad Sci U S A. 2002 Mar 19;99(6):3575-80. doi: 10.1073/pnas.052209199. Proc Natl Acad Sci U S A. 2002. PMID: 11904419 Free PMC article.

8

Domains of E1A that bind p105Rb, p130, and p300 are required to block nerve growth factor-induced neurite growth in PC12 cells.

Kalman D, Whittaker K, Bishop JM, O'Lague PH. Kalman D, et al. Among authors: o lague ph. Mol Biol Cell. 1993 Apr;4(4):353-61. doi: 10.1091/mbc.4.4.353. Mol Biol Cell. 1993. PMID: 8507895 Free PMC article.

9

Nerve growth factor acts through cAMP-dependent protein kinase to increase the number of sodium channels in PC12 cells.

Kalman D, Wong B, Horvai AE, Cline MJ, O'Lague PH. Kalman D, et al. Among authors: o lague ph. Neuron. 1990 Mar;4(3):355-66. doi: 10.1016/0896-6273(90)90048-k. Neuron. 1990. PMID: 1690563

10

Calcium-dependent inactivation of the dihydropyridine-sensitive calcium channels in GH3 cells.

Kalman D, O'Lague PH, Erxleben C, Armstrong DL. Kalman D, et al. Among authors: o lague ph. J Gen Physiol. 1988 Oct;92(4):531-48. doi: 10.1085/jgp.92.4.531. J Gen Physiol. 1988. PMID: 2849631 Free PMC article.

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