Zobrazeno 1 - 10
of 164
pro vyhledávání: '"Meyrick, Barbara"'
Autor:
Talati, Megha, Seeley, Erin, Ihida-Stansbury, Kaori, Delisser, Horace, McDonald, Hayes, Ye, Fei, Zhang, Xueqiong, Shyr, Yu, Caprioli, Richard, Meyrick, Barbara
Publikováno v:
Pulmonary Circulation, 2012 Jul 01. 2(3), 340-351.
Externí odkaz:
https://www.jstor.org/stable/10.4103/2045-8932.101645
Autor:
Meyrick Barbara, Caestecker Mark De
Publikováno v:
Respiratory Research, Vol 2, Iss 4, Pp 193-197 (2001)
Abstract Several recent papers have shown that both familial primary pulmonary hypertension (FPPH) and sporadic primary pulmonary hypertension (PPH) may have a common etiology that is associated with the inheritance and/or spontaneous development of
Externí odkaz:
https://doaj.org/article/6a8a5e20f5574a83a1950c59baac998d
Autor:
Meyrick, Barbara, Reid, Lynne
Publikováno v:
The Journal of Cell Biology, 1975 Nov 01. 67(2), 320-344.
Externí odkaz:
https://www.jstor.org/stable/1607650
Autor:
Stewart, Douglas R., Cogan, Joy D., Kramer, Mordechai R., Miller, Wallace T., Jr, Christiansen, Leif E., Pauciulo, Michael W., Messiaen, Ludwine M., Tu, George S., Thompson, William H., Pyeritz, Reed E., Ryu, Jay H., Nichols, William C., Kodama, Makoto, Meyrick, Barbara O., Ross, David J.
Publikováno v:
In Chest September 2007 132(3):798-808
Autor:
Talati, Megha, Meyrick, Barbara, Peebles, R. Stokes, Jr., Davies, Sean S., Dworski, Ryszard, Mernaugh, Ray, Mitchell, Daphne, Boothby, Mark, Roberts, L. Jackson, II, Sheller, James R.
Publikováno v:
In Free Radical Biology and Medicine 2006 40(7):1210-1219
Autor:
Chen, Jian-xiong, Meyrick, Barbara
Publikováno v:
In Laboratory Investigation 1 February 2004 84(2):182-190
Autor:
Davies, Sean S *, Talati, Megha, Wang, Xiahong, Mernaugh, Raymond L, Amarnath, Venkataraman, Fessel, Joshua *, Meyrick, Barbara O, Sheller, James, Roberts, L.Jackson, II *
Publikováno v:
In Free Radical Biology and Medicine 2004 36(9):1163-1174
Autor:
Phillips John A, Newman John, Robinson Linda, Geraci Mark, Cogan Joy, West James, Lane Kirk, Meyrick Barbara, Loyd Jim
Publikováno v:
BMC Medical Genomics, Vol 1, Iss 1, p 45 (2008)
Abstract Background While BMPR2 mutation strongly predisposes to pulmonary arterial hypertension (PAH), only 20% of mutation carriers develop clinical disease. This finding suggests that modifier genes contribute to FPAH clinical expression. Since mo
Externí odkaz:
https://doaj.org/article/442e13e837e046289a4837ec9a3359f4