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Mustapha Amyere

Showing results (1-10 of 17) with videos related to

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European Journal of Human Genetics : EJHG|April 28, 2006
Localization of candidate regions for a novel gene for Kartagener syndromeIlse Gutierrez-Roelens, Thierry Sluysmans, Mark Jorissen, et al.
Journal of Cell Science|September 2, 2004
v-Src accelerates spontaneous motility via phosphoinositide 3-kinase, phospholipase C and phospholipase D, but abrogates chemotaxis in Rat-1 and MDCK cellsAnna Platek, Marcel Mettlen, Isabelle Camby, et al.
The Journal of Investigative Dermatology|March 4, 2011
KITLG mutations cause familial progressive hyper- and hypopigmentationMustapha Amyere, Thomas Vogt, Joe Hoo, et al.
International Journal of Medical Microbiology : IJMM|March 14, 2002
Origin, originality, functions, subversions and molecular signalling of macropinocytosisMustapha Amyere, Marcel Mettlen, Patrick Van Der Smissen, et al.
Traffic (Copenhagen, Denmark)|April 29, 2006
Src triggers circular ruffling and macropinocytosis at the apical surface of polarized MDCK cellsMarcel Mettlen, Anna Platek, Patrick Van Der Smissen, et al.
Molecular Syndromology|January 8, 2015
Common somatic alterations identified in maffucci syndrome by molecular karyotypingMustapha Amyere, Anne Dompmartin, Vinciane Wouters, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 2012
Giant cell tumor occurring in familial Paget's disease of bone: report of clinical characteristics and linkage analysis of a large pedigreeFernando Gianfrancesco, Domenico Rendina, Daniela Merlotti, et al.
Journal of Hypertension|January 17, 2009
Rare presentation of familial paraganglioma without evidence of mutation in the SDH, RET and VHL genes: towards further genetic heterogeneityAlexandre Persu, Mustapha Amyere, Ilse Gutierrez-Roelens, et al.
American Journal of Medical Genetics. Part A|November 7, 2015
Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetusAntoine B Christiaens, Pierre M L Deprez, Mustapha Amyere, et al.
American Journal of Human Genetics|February 5, 2013
Somatic uniparental isodisomy explains multifocality of glomuvenous malformationsMustapha Amyere, Virginie Aerts, Pascal Brouillard, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
European Journal of Human Genetics : EJHG|April 28, 2006
Localization of candidate regions for a novel gene for Kartagener syndromeIlse Gutierrez-Roelens, Thierry Sluysmans, Mark Jorissen, et al.
Journal of Cell Science|September 2, 2004
v-Src accelerates spontaneous motility via phosphoinositide 3-kinase, phospholipase C and phospholipase D, but abrogates chemotaxis in Rat-1 and MDCK cellsAnna Platek, Marcel Mettlen, Isabelle Camby, et al.
The Journal of Investigative Dermatology|March 4, 2011
KITLG mutations cause familial progressive hyper- and hypopigmentationMustapha Amyere, Thomas Vogt, Joe Hoo, et al.
International Journal of Medical Microbiology : IJMM|March 14, 2002
Origin, originality, functions, subversions and molecular signalling of macropinocytosisMustapha Amyere, Marcel Mettlen, Patrick Van Der Smissen, et al.
Traffic (Copenhagen, Denmark)|April 29, 2006
Src triggers circular ruffling and macropinocytosis at the apical surface of polarized MDCK cellsMarcel Mettlen, Anna Platek, Patrick Van Der Smissen, et al.
Molecular Syndromology|January 8, 2015
Common somatic alterations identified in maffucci syndrome by molecular karyotypingMustapha Amyere, Anne Dompmartin, Vinciane Wouters, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 2012
Giant cell tumor occurring in familial Paget's disease of bone: report of clinical characteristics and linkage analysis of a large pedigreeFernando Gianfrancesco, Domenico Rendina, Daniela Merlotti, et al.
Journal of Hypertension|January 17, 2009
Rare presentation of familial paraganglioma without evidence of mutation in the SDH, RET and VHL genes: towards further genetic heterogeneityAlexandre Persu, Mustapha Amyere, Ilse Gutierrez-Roelens, et al.
American Journal of Medical Genetics. Part A|November 7, 2015
Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetusAntoine B Christiaens, Pierre M L Deprez, Mustapha Amyere, et al.
American Journal of Human Genetics|February 5, 2013
Somatic uniparental isodisomy explains multifocality of glomuvenous malformationsMustapha Amyere, Virginie Aerts, Pascal Brouillard, et al.
Pageof 2