Your search returned 29 results.

Results
	1.	To aggregate or not to aggregate... [electronic resource] by Neerman-Arbez, M Producer: 20071207 In: Journal of thrombosis and haemostasis : JTH vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Fibrinogen gene mutations accounting for congenital afibrinogenemia. [electronic resource] by Neerman-Arbez, M Producer: 20010802 In: Annals of the New York Academy of Sciences vol. 936 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The molecular basis of inherited afibrinogenaemia. [electronic resource] by Neerman-Arbez, M Producer: 20020122 In: Thrombosis and haemostasis vol. 86 Availability: No items available. Save to lists Add to cart (remove)
	4.	Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins. [electronic resource] by Vu, D Neerman-Arbez, M Producer: 20070918 In: Journal of thrombosis and haemostasis : JTH vol. 5 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Novel, non-crinophagic, degradation of connecting peptide in transformed pancreatic beta cells. [electronic resource] by Neerman-Arbez, M Halban, P A Producer: 19930907 In: The Journal of biological chemistry vol. 268 Availability: No items available. Save to lists Add to cart (remove)
	6.	Levels of the conversion endoproteases PC1 (PC3) and PC2 distinguish between insulin-producing pancreatic islet beta cells and non-beta cells. [electronic resource] by Neerman-Arbez, M Cirulli, V Halban, P A Producer: 19940628 In: The Biochemical journal vol. 300 ( Pt 1) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Slow cleavage at the proinsulin B-chain/connecting peptide junction associated with low levels of endoprotease PC1/3 in transformed beta cells. [electronic resource] by Neerman-Arbez, M Sizonenko, S V Halban, P A Producer: 19930907 In: The Journal of biological chemistry vol. 268 Availability: No items available. Save to lists Add to cart (remove)
	8.	Local chromatin interactions contribute to expression of the fibrinogen gene cluster. [electronic resource] by Espitia Jaimes, C Fish, R J Neerman-Arbez, M Producer: 20191223 In: Journal of thrombosis and haemostasis : JTH vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Deletion of the fibrinogen [correction of fibrogen] alpha-chain gene (FGA) causes congenital afibrogenemia. [electronic resource] by Neerman-Arbez, M Honsberger, A Antonarakis, S E Morris, M A Producer: 19990225 In: The Journal of clinical investigation vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster. [electronic resource] by Neerman-Arbez, M Antonarakis, S E Honsberger, A Morris, M A Producer: 20000214 In: European journal of human genetics : EJHG vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management. [electronic resource] by Casini, A Neerman-Arbez, M Ariëns, R A de Moerloose, P Producer: 20160225 In: Journal of thrombosis and haemostasis : JTH vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Human proinsulin conversion in the regulated and the constitutive pathways of transfected AtT20 cells. [electronic resource] by Irminger, J C Vollenweider, F M Neerman-Arbez, M Halban, P A Producer: 19940225 In: The Journal of biological chemistry vol. 269 Availability: No items available. Save to lists Add to cart (remove)
	13.	Coexisting dysfibrinogenemia (gamma Arg275His) and FV Leiden associated with thrombosis (Fibrinogen Crete). [electronic resource] by Travlou, A Gialeraki, A Merkouri, E Politou, M Sfyridaki, A Neerman-Arbez, M Producer: 20101129 In: Thrombosis research vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	High incidence of ectopic nucleolar organizer regions in human testicular tumors. [electronic resource] by Neerman-Arbez, M DeLozier-Blanchet, C D Bolle, J F Rondez, R Morris, M Producer: 19930318 In: Cancer genetics and cytogenetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G-->T. [electronic resource] by Attanasio, C de Moerloose, P Antonarakis, S E Morris, M A Neerman-Arbez, M Producer: 20010426 In: Blood vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion. [electronic resource] by Vu, D de Moerloose, P Batorova, A Lazur, J Palumbo, L Neerman-Arbez, M Producer: 20060727 In: Journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation. [electronic resource] by Casini, A Brungs, T Lavenu-Bombled, C Vilar, R Neerman-Arbez, M de Moerloose, P Producer: 20180326 In: Journal of thrombosis and haemostasis : JTH vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream. [electronic resource] by Robert-Ebadi, H de Moerloose, P El Khorassani, M El Khattab, M Neerman-Arbez, M Producer: 20090824 In: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Successful pregnancy under fibrinogen substitution in a woman with congenital afibrinogenaemia complicated by a postpartum venous thrombosis. [electronic resource] by Lebreton, A Casini, A Alhayek, R Kouteich, K L Neerman-Arbez, M de Moerloose, P Producer: 20150804 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature. [electronic resource] by Casini, A Sokollik, C Lukowski, S W Lurz, E Rieubland, C de Moerloose, P Neerman-Arbez, M Producer: 20160809 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search

Availability

Authors

Topics

Languages

Your search returned 29 results.