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44篇 您的检索式：作者名="Pfarr"

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	题名	作者	年代	出处	被引量
1	Darsentan:an effective endothelin A receptor antagonist for treatment of hypertension显示文摘	Nakov R Pfarr E Eberle S	2002	Am J Hypertens2002，15，：	1
2	Hemodynamic and clinical onset in patients with hereditary pulmonary arterial hypertension and BMPR2 mutations显示文摘	Pfarr N Szamalek-Hoegel J Fischer C	2011	Respir Res2011，12，1：	1
3	Trafficking of Crumbs3 during cytokinesis is crucial for lumen formation显示文摘	Schlüter MA Pfarr CS Pieczynski J		0，，22：	1
4	Ultra-potent antibodies against respiratory syncytial virus : effects of binding kinetics and binding valence on viral neutralization 显示文摘	Wu H Pfarr DS Tang Y	2005	J Mol Biol2005，350，1：	1
5	Immunoprophylaxis of RSVinfection:advancing from RSV-IGIV to palivizumab and motaviz-umab显示文摘	Wu H Pfarr DS Losonsky GA	2008	Curr Top Microbiol Immunol2008，317，：	1
6	Subclinical hyperthy- roidism due to a thyrotropin receptor (TSHR) gene mutation (S505R)显示文摘	Pohlenz J Pfarr N Kruger S	2006	ActaPaediatr2006，95，12：	1
7	Ultra-potent antibodies against respiratory syncytial virus: effects of binding kinetics and binding valence on viral neutralization显示文摘	Wu H Pfarr DS Tang Y	2005	J Mol Biol2005，350，1：	1
8	Mouse JunD negatively regulates fibroblast growth and antagonizes transformation by ras显示文摘	Pfarr CM Mechta F Spyron G	1994	Cell1994，76，：	1
9	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2(THOX2)gene显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol(Oxf)2006，65，6：	1
10	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) gene显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol2006，65，6：	1
11	Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation(A593V)显示文摘	Fricke-Otto S Pfarr N Muhlenberg R	2005	Exp Clin Endocrinol Diabetes2005，113，10：	1
12	Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart dis- ease associated pulmonary arterial hypertension显示文摘	Pfarr N Fischer C Ehlken N	2013	Respir Res2013，14，1：	1
13	Congenital primary hypothyroidism in a turkish family caused by a homozygons nonsense mutation(R609X)in the thyrotropin receptor gene显示文摘	Richter-Unruh A Hauffa BP Pfarr N	2004	Thyroid2004，14，11：	1
14	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) gene 显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol (Oxf)2006，65，：	1
15	Htra-potent antibodies against respiratory syncytial virus:effects of binding kinetics and binding valence on viral neutralization显示文摘	Wu H Pfarr DS Tang Y	2005	J Mol Biol2005，350，1：	1
16	Therapeutic use of the natriuretic peptide ularitide in acute renal failure显示文摘	Meyer M Pfarr E Schirmer G	1999	Ren Fail1999，1，1：	1
17	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2(THOX2)gene显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol(Oxf)2006，65，6：	1
18	Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart disease associated pulmonary arterial hypertension 显示文摘	Pfarr N Fischer C Ehlken N	2013	Respir Res2013，14，：	1
19	Endol6,a large muhidomain protein found on the surface and ECM of endodermal cells during sea urchin gastrulation,binds calcium显示文摘	Soltysik M Klinzing D Pfarr K	1994	Dev Biol1994，165，1：	1
20	Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 ( THOX2 ) gene 显示文摘	Pfarr N Korsch E Kaspers S	2006	Clin Endocrinol ( Oxf)2006，65，6：	1

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