000			02200 a2200697 4500
005			20250515180141.0
264		0	_c20091027
008			200910s 0 0 eng d
022			_a1528-0020
024	7		_a10.1182/blood-2009-01-197640 _2doi
040			_aNLM _beng _cNLM
100	1		_aRoumenina, Lubka T
245	0	0	_aHyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome. _h[electronic resource]
260			_bBlood _cSep 2009
300			_a2837-45 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aAged
650	0	4	_aAged, 80 and over
650	0	4	_aCells, Cultured
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aCohort Studies
650	0	4	_aComplement Activation _xgenetics
650	0	4	_aComplement C3-C5 Convertases _xgenetics
650	0	4	_aComplement System Proteins _xgenetics
650	0	4	_aEndothelial Cells _xmetabolism
650	0	4	_aFamily
650	0	4	_aFemale
650	0	4	_aHemolytic-Uremic Syndrome _xgenetics
650	0	4	_aHumans
650	0	4	_aInfant
650	0	4	_aInfant, Newborn
650	0	4	_aMale
650	0	4	_aMiddle Aged
650	0	4	_aModels, Molecular
650	0	4	_aMutant Proteins _xphysiology
650	0	4	_aPedigree
650	0	4	_aYoung Adult
700	1		_aJablonski, Mathieu
700	1		_aHue, Christophe
700	1		_aBlouin, Jacques
700	1		_aDimitrov, Jordan D
700	1		_aDragon-Durey, Marie-Agnes
700	1		_aCayla, Mathieu
700	1		_aFridman, Wolf H
700	1		_aMacher, Marie-Alice
700	1		_aRibes, David
700	1		_aMoulonguet, Luc
700	1		_aRostaing, Lionel
700	1		_aSatchell, Simon C
700	1		_aMathieson, Peter W
700	1		_aSautes-Fridman, Catherine
700	1		_aLoirat, Chantal
700	1		_aRegnier, Catherine H
700	1		_aHalbwachs-Mecarelli, Lise
700	1		_aFremeaux-Bacchi, Veronique
773	0		_tBlood _gvol. 114 _gno. 13 _gp. 2837-45
856	4	0	_uhttps://doi.org/10.1182/blood-2009-01-197640 _zAvailable from publisher's website
999			_c18999764 _d18999764