Tietjen I - Search Results

1

Single-cell transcriptional analysis of neuronal progenitors.

Tietjen I, Rihel JM, Cao Y, Koentges G, Zakhary L, Dulac C. Tietjen I, et al. Neuron. 2003 Apr 24;38(2):161-75. doi: 10.1016/s0896-6273(03)00229-0. Neuron. 2003. PMID: 12718852 Free article.

2

Single-cell transcriptional profiles and spatial patterning of the mammalian olfactory epithelium.

Tietjen I, Rihel J, Dulac CG. Tietjen I, et al. Int J Dev Biol. 2005;49(2-3):201-7. doi: 10.1387/ijdb.041939it. Int J Dev Biol. 2005. PMID: 15906233 Free article.

3

Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning.

Bae BI, Tietjen I, Atabay KD, Evrony GD, Johnson MB, Asare E, Wang PP, Murayama AY, Im K, Lisgo SN, Overman L, Šestan N, Chang BS, Barkovich AJ, Grant PE, Topçu M, Politsky J, Okano H, Piao X, Walsh CA. Bae BI, et al. Among authors: tietjen i. Science. 2014 Feb 14;343(6172):764-8. doi: 10.1126/science.1244392. Science. 2014. PMID: 24531968 Free PMC article.

4

EMX2-independent familial schizencephaly: clinical and genetic analyses.

Tietjen I, Erdogan F, Currier S, Apse K, Chang BS, Hill RS, Lee CK, Walsh CA. Tietjen I, et al. Am J Med Genet A. 2005 Jun 1;135(2):166-70. doi: 10.1002/ajmg.a.30734. Am J Med Genet A. 2005. PMID: 15887302

5

Comprehensive EMX2 genotyping of a large schizencephaly case series.

Tietjen I, Bodell A, Apse K, Mendonza AM, Chang BS, Shaw GM, Barkovich AJ, Lammer EJ, Walsh CA. Tietjen I, et al. Am J Med Genet A. 2007 Jun 15;143A(12):1313-6. doi: 10.1002/ajmg.a.31767. Am J Med Genet A. 2007. PMID: 17506092

6

Disease-associated mutations affect GPR56 protein trafficking and cell surface expression.

Jin Z, Tietjen I, Bu L, Liu-Yesucevitz L, Gaur SK, Walsh CA, Piao X. Jin Z, et al. Among authors: tietjen i. Hum Mol Genet. 2007 Aug 15;16(16):1972-85. doi: 10.1093/hmg/ddm144. Epub 2007 Jun 18. Hum Mol Genet. 2007. PMID: 17576745

7

Novel mutations in scavenger receptor BI associated with high HDL cholesterol in humans.

Brunham LR, Tietjen I, Bochem AE, Singaraja RR, Franchini PL, Radomski C, Mattice M, Legendre A, Hovingh GK, Kastelein JJ, Hayden MR. Brunham LR, et al. Among authors: tietjen i. Clin Genet. 2011 Jun;79(6):575-81. doi: 10.1111/j.1399-0004.2011.01682.x. Clin Genet. 2011. PMID: 21480869

8

Identification of four novel genes contributing to familial elevated plasma HDL cholesterol in humans.

Singaraja RR, Tietjen I, Hovingh GK, Franchini PL, Radomski C, Wong K, vanHeek M, Stylianou IM, Lin L, Wang L, Mitnaul L, Hubbard B, Winther M, Mattice M, Legendre A, Sherrington R, Kastelein JJ, Akinsanya K, Plump A, Hayden MR. Singaraja RR, et al. Among authors: tietjen i. J Lipid Res. 2014 Aug;55(8):1693-701. doi: 10.1194/jlr.M048710. Epub 2014 Jun 2. J Lipid Res. 2014. PMID: 24891332 Free PMC article.

9

Two novel mutations in apolipoprotein C3 underlie atheroprotective lipid profiles in families.

Bochem AE, van Capelleveen JC, Dallinga-Thie GM, Schimmel AW, Motazacker MM, Tietjen I, Singaraja RR, Hayden MR, Kastelein JJ, Stroes ES, Hovingh GK. Bochem AE, et al. Among authors: tietjen i. Clin Genet. 2014 May;85(5):433-40. doi: 10.1111/cge.12201. Epub 2013 Jun 24. Clin Genet. 2014. PMID: 23701270

10

Increased risk of coronary artery disease in Caucasians with extremely low HDL cholesterol due to mutations in ABCA1, APOA1, and LCAT.

Tietjen I, Hovingh GK, Singaraja R, Radomski C, McEwen J, Chan E, Mattice M, Legendre A, Kastelein JJ, Hayden MR. Tietjen I, et al. Biochim Biophys Acta. 2012 Mar;1821(3):416-24. doi: 10.1016/j.bbalip.2011.08.006. Epub 2011 Aug 19. Biochim Biophys Acta. 2012. PMID: 21875686

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