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LinkedIn: Maila Giannandrea | LinkedIn
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Visualizza il profilo professionale di Maila Giannandrea su LinkedIn. LinkedIn è la rete professionale più grande al mondo utilizzata dai professionisti come Maila Giannandrea per trovare collegamenti che possano segnalare candidati, esperti e business partner.
LinkedIn: Maila Giannandrea | LinkedIn
Maila Giannandreas berufliches Profil anzeigen LinkedIn ist das weltweit größte berufliche Netzwerk, das Fach- und Führungskräften wie Maila Giannandrea ...
Facebook: Maila Giannandrea | Facebook
Maila Giannandrea is on Facebook. Join Facebook to connect with Maila Giannandrea and others you may know. Facebook gives people the power to share and makes the ...
Dokumente zum Namen
A CTNNA3 compound heterozygous deletion implicates a role for...
www.scienceopen.com
Contributors. Elena Bacchelli. Fabiola Ceroni. Dalila Pinto. Silvia Lomartire. Maila Giannandrea. Patrizia D'Adamo. Elena Bonora. Piero Parchi.
д-р радослава василева въжарова, софийски Каталог
nt-cmb.medun.acad.bg
Bacchelli Elena, Fabiola Ceroni, Dalila Pinto, Silvia Lomartire, Maila Giannandrea, Patrizia. D'Adamo, Elena Bonora, Piero Parchi, Raffaella Tancredi, Agatino Battaglia and Elena. Maestrini. A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum ...
Wissenschaftliche Veröffentlichungen
The American Journal of Human Genetics | Vol 95, Issue 6, Pages...
www.sciencedirect.com
McLean, Maila Giannandrea, ... Paul J. Lockhart. Download PDF.
A CTNNA3 compound heterozygous deletion implicates a role for αT ...jneurodevdisorders.biomedcentral.com › articles
jneurodevdisorders.biomedcentral.com
· Maila Giannandrea & Patrizia D'Adamo. Vita-Salute San Raffaele University, MilanItaly. Patrizia D'Adamo. Unit of Medical Genetics, ...
Veröffentlichungen allgemein
A CTNNA3 compound heterozygous deletion implicates a role for...
link.springer.com
... Lomartire · (1); Maila Giannandrea · (6); Patrizia D'Adamo · ...
Artikel & Meinungen
The intellectual disability protein RAB39B selectively regulates...
www.nature.com
· Maria Lidia Mignogna, Maila Giannandrea, Antonia Gurgone & Patrizia D'Adamo. F. Hoffmann-La Roche AG, pRED Pharma Research & Early ...
Sonstiges
Mutations in RAB39B Cause X-Linked Intellectual Disability and...
slideplayer.com
... Maila Giannandrea, Charles A. Galea, Jessica R. Riseley, Sarah E.M. Stephenson, Elizabeth Fitzpatrick, Stefan A. Haas, Kate Pope, Kirk J. Hogan, ...
Consciousness - Yahoo Groups
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Maila Giannandrea, Fabrizia C. Guarnieri, Niels H. Gehring, Elena Monzani, Fabio Benfenati, Andreas E. Kulozik, Flavia Valtorta. Temperature ...
Maila Giannandrea | LinkedIn
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Maila Giannandrea Location Milan Area, Italy Industry Research Join LinkedIn and access Maila Giannandrea’s full profile.
Mutations in the Small GTPase Gene RAB39B Are Responsible for...
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... in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly Maila Giannandrea,.
Maila%20Giannandrea: مفت ڈاؤنلوڈ. ای بک لائبریری۔ Z-Library پر آن...
ur.booksc.eu
Maila%20Giannandrea: مفت ڈاؤنلوڈ. ای بک لائبریری۔ Z-Library پر آن لائن کتابوں کی دکانیں | BookSC. Download books for free. Find books
Epilepsy: Giannandrea, Maila - Expertscape.com
expertscape.com
Maila Giannandrea has special expertise in Epilepsy
A CTNNA3 compound heterozygous deletion implicates a role for...
cyberleninka.org
... paper in Biological sciences , author of scholarly article — Elena Bacchelli, Fabiola Ceroni, Dalila Pinto, Silvia Lomartire, Maila Giannandrea, et al.
Maila Giannandrea
www.infona.pl
Advances in understanding the etiology of Parkinson disease have been driven by the identification of causative mutations in families. Genetic analysis of an ...
Human cytomegalovirus DNA polymerase catalytic subunit pUL54...
research.monash.edu
Gualtiero Alvisi, Alessandro Ripalti, Apollinaire Ngankeu, Maila Giannandrea, Stefano G Caraffi, Manisha Dias, David Andrew Jans · Biochemistry & Molecular ...
HHV5 - Polymerase - Polbasepolbase.neb.com › polymerases › 359-hhv5
polbase.neb.com
2006, Gualtiero Alvisi, Alessandro Ripalti, Apollinaire Ngankeu, Maila Giannandrea, Stefano G Caraffi, Manisha M Dias, David A Jans, Human cytomegalovirus ...
Increased dosage of RAB39B affects neuronal development and could...
moh-it.pure.elsevier.com
Increased dosage of RAB39B affects neuronal development and could explain the cognitive impairment in male patients with distal Xq28 copy number gains. Lieselot Vanmarsenille, Maila Giannandrea, Nathalie Fieremans, Jelle Verbeeck, Stefanie Belet, Martine Raynaud, Annick Vogels, Katrin Männik, Katrin Õunap, ...
Mutations in the Small GTPase Gene RAB39B Are Responsible for...
research.sahmri.org.au
Maila Giannandrea, Veronica Bianchi, Maria Lidia Mignogna, Alessandra Sirri, Salvatore Carrabino, Errico D'Elia, Matteo Vecellio, Silvia ...
Increased dosage of RAB39B affects neuronal development and ...researchportal.vub.be › publications
researchportal.vub.be
Lieselot Vanmarsenille, Maila Giannandrea, Nathalie Fieremans, Jelle Verbeeck, Stefanie Belet, Martine Raynaud, Annick Vogels, Katrin Männik, Katrin Õunap, ...
Lieselot Vanmarsenille | Research Portal
researchportal.be
Authors: Lieselot Vanmarsenille, Maila Giannandrea, Nathalie Fieremans, Jelle Verbeeck, Stefanie Belet, Martine Raynaud, Annick Vogels, Katrin Männik, ...
[PDF] Mutations in RAB39B cause X-linked intellectual disability and...
www.semanticscholar.org
Semantic Scholar extracted view of
The W356× Syn I variant is poorly expressed in transfected HeLa cells.
figshare.com
posted on , 18:49 by Maila Giannandrea Fabrizia C. Guarnieri Niels H. Gehring Elena Monzani Fabio Benfenati Andreas E. Kulozik Flavia Valtorta.
The intellectual disability protein RAB39B selectively regulates...
jhu.pure.elsevier.com
Maria Lidia Mignogna, Maila Giannandrea, Antonia Gurgone, Francesca Fanelli, Francesco Raimondi, Lisa Mapelli, Silvia Bassani, Huaqiang ...
The W356× Syn I variant is not targeted to nerve terminals in either...
figshare.com
Maila Giannandrea · Fabrizia C. Guarnieri · Niels H. Gehring · Elena Monzani · Fabio Benfenati · Andreas E. Kulozik · Flavia Valtorta.
Increased Dosage of RAB39B Affects Neuronal Development and Could...
www.bionity.com
Autoren: Lieselot Vanmarsenille, Maila Giannandrea, Nathalie Fieremans, Jelle Verbeeck, Stefanie Belet, Martine Raynaud, Annick Vogels, ...
homozygous nonsense mutation: Topics by WorldWideScience.org
worldwidescience.org
Maila Giannandrea. Full Text Available Synapsins are a family of neuronal phosphoproteins associated with the cytosolic surface of synaptic vesicles.
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