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26篇 您的检索式：作者名="Raam"

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	题名	作者	年代	出处	被引量
1	First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure显示文摘	Jaspers N G Raams A Silengo M C	2007	Am J Hum Genet2007，80，3：	1
2	Mechanism and specificity of the human paracaspase MALT1 显示文摘	Hachmann J Snipas S J van Raam B J	2012	Biochem J2012，443，1：	1
3	Mitochondria in Neutrophil Apoptosis显示文摘	B. J. Raam A. J. Verhoeven T. W. Kuijpers	2006	International Journal of Hematology2006，，3：	1
4	Holoprosencephaly:a guide to diagnosis and clinical management显示文摘	Raam MS Solomon BD Muenke M		0，，06：	1
5	Upgrading of wakefield browncoal from south Australia显示文摘	Ruyter H P Van Raam L van der Poel H	1984	Fuel Processing Technology1984，9，2：	1
6	Upgrading of wake field brown coal from south Australia显示文摘	RUYTER H P van RAAM L van der POEL H	1984	Fuel Process Technol1984，9，2：	1
7	Analysis of a Physician Tool for Evaluating Dysphagia on an Inpatient Stroke Unit: The Modified Mann Assessment of Swallowing Ability显示文摘	Nader Antonios Giselle Carnaby-Mann Michael Crary Leslie Miller Holly Hubbard Kelly Hood Raam Sambandam Andrew Xavier Scott Silliman	2010	Journal of Stroke and Cerebrovascular Diseases2010，，1：	1
8	Changes in gene expression of granulocytes during in vivo granulocyte colonystimulating factor/dexamethasone mobilization for transfusion purposes显示文摘	Drewniak A van Raam BJ Geissler J	2009	Blood2009，113，23：	1
9	Proliferative versus apoptotie functions of easpase-8 Hetero or homo:the caspase-8 dimer controls cell fate 显示文摘	van Raam BJ Salvesen GS	2012	Bioehim Biophys Aeta2012，1824，1：	1
10	A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis显示文摘	Niedernhofer LJ Garinis GA Raams A	2006	Nature2006，444，7122：	1
11	Proliferative versus apoptotic functions of caspase-8 Hetero or homo:the caspase-8 dimer controls cellfate显示文摘	van Raam BJ Salvesen GS		0，，01：	1
12	First reported patient with human ERCC1 deficiency has eerehro oculo facio skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure显示文摘	Jaspers NG Raams A Silengo MC	2007	Am J Hum Genet2007，80，3：	1
13	Evidence for inheritance in patients with VACTERL association 显示文摘	Solomon BD Pineda-Alvarez DE Raam MS	2010	Hum Genet2010，127，：	1
14	First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and se- vere developmental failure 显示文摘	Jaspers NGJ Raams A Silengo MC	2007	Am J Hum Genet2007，80，3：	1
15	Holoprosencephaly:a guide to diagnosis and clinical management显示文摘	Raam MS Solomon BD Muenke M	2011	Indian Pediatr2011，48，6：	1
16	Analysis of component findings in 79 patients diagnosed with VACTERL association显示文摘	Solomon BD Pineda-Alvarez DE Raam MS		0，，09：	1
17	Specific disruption of hipp- ocampal mossy fiber synapses in a mouse model of familial Alzhei- mer's disease显示文摘	Wilke SA Raam T Antonios JK	2014	PLoS One2014，9，84：	1
18	Holoprosencephaly: a guide to diagnosis and clinical management 显示文摘	Raam MS Solomon BD Muenke M	2011	Indian Pediatr2011，48，6：	1
19	Evidence for inheritance in patients with VACTERL association显示文摘	Solomon BD Pineda-Alvarez DE Raam MS	2010	Hum Genet2010，127，6：	1
20	Mitochondria in neutrophil apoptosis显示文摘	van Raam BJ Verhoeven AJ Kuijpers TW	2006	Int J Hematol2006，84，3：	1

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