Asilmaz E - Search Results

1

Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss.

Simpson MA, Irving MD, Asilmaz E, Gray MJ, Dafou D, Elmslie FV, Mansour S, Holder SE, Brain CE, Burton BK, Kim KH, Pauli RM, Aftimos S, Stewart H, Kim CA, Holder-Espinasse M, Robertson SP, Drake WM, Trembath RC. Simpson MA, et al. Among authors: asilmaz e. Nat Genet. 2011 Mar 6;43(4):303-5. doi: 10.1038/ng.779. Nat Genet. 2011. PMID: 21378985

2

Biomedical impact of splicing mutations revealed through exome sequencing.

Taneri B, Asilmaz E, Gaasterland T. Taneri B, et al. Among authors: asilmaz e. Mol Med. 2012 Mar 30;18(1):314-9. doi: 10.2119/molmed.2011.00126. Mol Med. 2012. PMID: 22160217 Free PMC article. Review.

3

Neurotransmitter receptor genotypes associated with mental and behavioral disorders.

Varoglu E, Seytanoglu A, Asilmaz E, Taneri B. Varoglu E, et al. Among authors: asilmaz e. Per Med. 2017 Jul;14(4):327-338. doi: 10.2217/pme-2016-0100. Epub 2017 Jun 22. Per Med. 2017. PMID: 29749833

4

Host Genetics at the Intersection of Autoimmunity and COVID-19: A Potential Key for Heterogeneous COVID-19 Severity.

Karaderi T, Bareke H, Kunter I, Seytanoglu A, Cagnan I, Balci D, Barin B, Hocaoglu MB, Rahmioglu N, Asilmaz E, Taneri B. Karaderi T, et al. Among authors: asilmaz e. Front Immunol. 2020 Dec 22;11:586111. doi: 10.3389/fimmu.2020.586111. eCollection 2020. Front Immunol. 2020. PMID: 33414783 Free PMC article. Review.

5

Site and mechanism of leptin action in a rodent form of congenital lipodystrophy.

Asilmaz E, Cohen P, Miyazaki M, Dobrzyn P, Ueki K, Fayzikhodjaeva G, Soukas AA, Kahn CR, Ntambi JM, Socci ND, Friedman JM. Asilmaz E, et al. J Clin Invest. 2004 Feb;113(3):414-24. doi: 10.1172/JCI19511. J Clin Invest. 2004. PMID: 14755338 Free PMC article.

6

Foxa2 regulates lipid metabolism and ketogenesis in the liver during fasting and in diabetes.

Wolfrum C, Asilmaz E, Luca E, Friedman JM, Stoffel M. Wolfrum C, et al. Among authors: asilmaz e. Nature. 2004 Dec 23;432(7020):1027-32. doi: 10.1038/nature03047. Nature. 2004. PMID: 15616563

7

Identification and characterization of murine SCD4, a novel heart-specific stearoyl-CoA desaturase isoform regulated by leptin and dietary factors.

Miyazaki M, Jacobson MJ, Man WC, Cohen P, Asilmaz E, Friedman JM, Ntambi JM. Miyazaki M, et al. Among authors: asilmaz e. J Biol Chem. 2003 Sep 5;278(36):33904-11. doi: 10.1074/jbc.M304724200. Epub 2003 Jun 18. J Biol Chem. 2003. PMID: 12815040 Free article.

8

Stearoyl-CoA desaturase 1 deficiency increases fatty acid oxidation by activating AMP-activated protein kinase in liver.

Dobrzyn P, Dobrzyn A, Miyazaki M, Cohen P, Asilmaz E, Hardie DG, Friedman JM, Ntambi JM. Dobrzyn P, et al. Among authors: asilmaz e. Proc Natl Acad Sci U S A. 2004 Apr 27;101(17):6409-14. doi: 10.1073/pnas.0401627101. Epub 2004 Apr 19. Proc Natl Acad Sci U S A. 2004. PMID: 15096593 Free PMC article.

9

Stearoyl-CoA desaturase-1 deficiency reduces ceramide synthesis by downregulating serine palmitoyltransferase and increasing beta-oxidation in skeletal muscle.

Dobrzyn A, Dobrzyn P, Lee SH, Miyazaki M, Cohen P, Asilmaz E, Hardie DG, Friedman JM, Ntambi JM. Dobrzyn A, et al. Among authors: asilmaz e. Am J Physiol Endocrinol Metab. 2005 Mar;288(3):E599-607. doi: 10.1152/ajpendo.00439.2004. Epub 2004 Nov 23. Am J Physiol Endocrinol Metab. 2005. PMID: 15562249 Free article.

10

Acute leptin deficiency, leptin resistance, and the physiologic response to leptin withdrawal.

Montez JM, Soukas A, Asilmaz E, Fayzikhodjaeva G, Fantuzzi G, Friedman JM. Montez JM, et al. Among authors: asilmaz e. Proc Natl Acad Sci U S A. 2005 Feb 15;102(7):2537-42. doi: 10.1073/pnas.0409530102. Epub 2005 Feb 7. Proc Natl Acad Sci U S A. 2005. PMID: 15699332 Free PMC article.

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