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SOX17 Deficiency Mediates Pulmonary Hypertension: At the Crossroads of Sex, Metabolism, and Genetics.
Sangam S, Sun X, Schwantes-An TH, Yegambaram M, Lu Q, Shi Y, Cook T, Fisher A, Frump AL, Coleman A, Sun Y, Liang S, Crawford H, Lutz KA, Maun AD, Pauciulo MW, Karnes JH, Chaudhary KR, Stewart DJ, Langlais PR, Jain M, Alotaibi M, Lahm T, Jin Y, Gu H, Tang H, Nichols WC, Black SM, Desai AA. Sangam S, et al. Among authors: pauciulo mw. Am J Respir Crit Care Med. 2023 Apr 15;207(8):1055-1069. doi: 10.1164/rccm.202203-0450OC. Am J Respir Crit Care Med. 2023. PMID: 36913491 Free PMC article.
Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease.
Simon DK, Pankratz N, Kissell DK, Pauciulo MW, Halter CA, Rudolph A, Pfeiffer RF, Nichols WC, Foroud T; Parkinson Study Group-PROGENI Investigators. Simon DK, et al. Among authors: pauciulo mw. BMC Med Genet. 2010 Apr 1;11:53. doi: 10.1186/1471-2350-11-53. BMC Med Genet. 2010. PMID: 20356410 Free PMC article.
Mutations in DJ-1 are rare in familial Parkinson disease.
Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Shults CW, Foroud T, Nichols WC; Parkinson Study Group - PROGENI Investigators. Pankratz N, et al. Among authors: pauciulo mw. Neurosci Lett. 2006 Nov 20;408(3):209-13. doi: 10.1016/j.neulet.2006.09.003. Epub 2006 Sep 25. Neurosci Lett. 2006. PMID: 16997464 Free PMC article.
R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation.
Nichols WC, Marek DK, Pauciulo MW, Pankratz N, Halter CA, Rudolph A, Shults CW, Wojcieszek J, Foroud T; Parkinson Study Group - PROGENI Investigators. Nichols WC, et al. Among authors: pauciulo mw. Mov Disord. 2007 Jan 15;22(2):254-7. doi: 10.1002/mds.21233. Mov Disord. 2007. PMID: 17149721
Racial and ethnic differences in pulmonary arterial hypertension.
Al-Naamani N, Paulus JK, Roberts KE, Pauciulo MW, Lutz K, Nichols WC, Kawut SM. Al-Naamani N, et al. Among authors: pauciulo mw. Pulm Circ. 2017 Oct-Dec;7(4):793-796. doi: 10.1177/2045893217732213. Epub 2017 Sep 15. Pulm Circ. 2017. PMID: 28849992 Free PMC article.
Frequency of GBA variants in autopsy-proven multiple system atrophy.
Sklerov M, Kang UJ, Liong C, Clark L, Marder K, Pauciulo M, Nichols WC, Chung WK, Honig LS, Cortes E, Vonsattel JP, Alcalay RN. Sklerov M, et al. Mov Disord Clin Pract. 2017 Jul-Aug;4(4):574-581. doi: 10.1002/mdc3.12481. Epub 2017 Apr 3. Mov Disord Clin Pract. 2017. PMID: 28966932 Free PMC article.
84 results