Mani A - Search Results

1

Mutations in the Histone Modifier PRDM6 Are Associated with Isolated Nonsyndromic Patent Ductus Arteriosus.

Li N, Subrahmanyan L, Smith E, Yu X, Zaidi S, Choi M, Mane S, Nelson-Williams C, Behjati M, Kazemi M, Hashemi M, Fathzadeh M, Narayanan A, Tian L, Montazeri F, Mani M, Begleiter ML, Coon BG, Lynch HT, Olson EN, Zhao H, Ruland J, Lifton RP, Mani A. Li N, et al. Among authors: mani m, mani a. Am J Hum Genet. 2016 Jun 2;98(6):1082-1091. doi: 10.1016/j.ajhg.2016.03.022. Epub 2016 May 12. Am J Hum Genet. 2016. PMID: 27181681 Free PMC article.

2

Finding genetic contributions to sporadic disease: a recessive locus at 12q24 commonly contributes to patent ductus arteriosus.

Mani A, Meraji SM, Houshyar R, Radhakrishnan J, Mani A, Ahangar M, Rezaie TM, Taghavinejad MA, Broumand B, Zhao H, Nelson-Williams C, Lifton RP. Mani A, et al. Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):15054-9. doi: 10.1073/pnas.192582999. Epub 2002 Oct 30. Proc Natl Acad Sci U S A. 2002. PMID: 12409608 Free PMC article.

3

Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder.

Mani A, Radhakrishnan J, Farhi A, Carew KS, Warnes CA, Nelson-Williams C, Day RW, Pober B, State MW, Lifton RP. Mani A, et al. Proc Natl Acad Sci U S A. 2005 Feb 22;102(8):2975-9. doi: 10.1073/pnas.0409852102. Epub 2005 Jan 31. Proc Natl Acad Sci U S A. 2005. PMID: 15684060 Free PMC article.

4

LRP6 mutation in a family with early coronary disease and metabolic risk factors.

Mani A, Radhakrishnan J, Wang H, Mani A, Mani MA, Nelson-Williams C, Carew KS, Mane S, Najmabadi H, Wu D, Lifton RP. Mani A, et al. Among authors: mani ma. Science. 2007 Mar 2;315(5816):1278-82. doi: 10.1126/science.1136370. Science. 2007. PMID: 17332414 Free PMC article.

5

Wild-type LRP6 inhibits, whereas atherosclerosis-linked LRP6R611C increases PDGF-dependent vascular smooth muscle cell proliferation.

Keramati AR, Singh R, Lin A, Faramarzi S, Ye ZJ, Mane S, Tellides G, Lifton RP, Mani A. Keramati AR, et al. Among authors: mani a. Proc Natl Acad Sci U S A. 2011 Feb 1;108(5):1914-8. doi: 10.1073/pnas.1019443108. Epub 2011 Jan 18. Proc Natl Acad Sci U S A. 2011. PMID: 21245321 Free PMC article.

6

Low density lipoprotein (LDL) receptor-related protein 6 (LRP6) regulates body fat and glucose homeostasis by modulating nutrient sensing pathways and mitochondrial energy expenditure.

Liu W, Singh R, Choi CS, Lee HY, Keramati AR, Samuel VT, Lifton RP, Shulman GI, Mani A. Liu W, et al. Among authors: mani a. J Biol Chem. 2012 Mar 2;287(10):7213-23. doi: 10.1074/jbc.M111.286724. Epub 2012 Jan 9. J Biol Chem. 2012. PMID: 22232553 Free PMC article.

7

Rare nonconservative LRP6 mutations are associated with metabolic syndrome.

Singh R, Smith E, Fathzadeh M, Liu W, Go GW, Subrahmanyan L, Faramarzi S, McKenna W, Mani A. Singh R, et al. Among authors: mani a. Hum Mutat. 2013 Sep;34(9):1221-5. doi: 10.1002/humu.22360. Epub 2013 Jun 18. Hum Mutat. 2013. PMID: 23703864 Free PMC article.

8

A form of the metabolic syndrome associated with mutations in DYRK1B.

Keramati AR, Fathzadeh M, Go GW, Singh R, Choi M, Faramarzi S, Mane S, Kasaei M, Sarajzadeh-Fard K, Hwa J, Kidd KK, Babaee Bigi MA, Malekzadeh R, Hosseinian A, Babaei M, Lifton RP, Mani A. Keramati AR, et al. Among authors: mani a. N Engl J Med. 2014 May 15;370(20):1909-1919. doi: 10.1056/NEJMoa1301824. N Engl J Med. 2014. PMID: 24827035 Free PMC article.

9

The metabolic syndrome and DYRK1B.

Keramati AR, Fathzadeh M, Mani A. Keramati AR, et al. Among authors: mani a. N Engl J Med. 2014 Aug 21;371(8):785-6. doi: 10.1056/NEJMc1408235. N Engl J Med. 2014. PMID: 25140972 No abstract available.

10

Wnt signaling, de novo lipogenesis, adipogenesis and ectopic fat.

Song K, Wang S, Mani M, Mani A. Song K, et al. Among authors: mani m, mani a. Oncotarget. 2014 Nov 30;5(22):11000-3. doi: 10.18632/oncotarget.2769. Oncotarget. 2014. PMID: 25526027 Free PMC article.

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