Results
|
1321.
|
|
|
1322.
|
Dystroglycan on radial glia end feet is required for pial basement membrane integrity and columnar organization of the developing cerebral cortex. [electronic resource] by
- Myshrall, Timothy D
- Moore, Steven A
- Ostendorf, Adam P
- Satz, Jakob S
- Kowalczyk, Tom
- Nguyen, Huy
- Daza, Ray A M
- Lau, Charmaine
- Campbell, Kevin P
- Hevner, Robert F
Producer: 20130204
In:
Journal of neuropathology and experimental neurology vol. 71
Availability: No items available.
|
|
1323.
|
|
|
1324.
|
Virus entry. Lassa virus entry requires a trigger-induced receptor switch. [electronic resource] by
- Jae, Lucas T
- Raaben, Matthijs
- Herbert, Andrew S
- Kuehne, Ana I
- Wirchnianski, Ariel S
- Soh, Timothy K
- Stubbs, Sarah H
- Janssen, Hans
- Damme, Markus
- Saftig, Paul
- Whelan, Sean P
- Dye, John M
- Brummelkamp, Thijn R
Producer: 20140711
In:
Science (New York, N.Y.) vol. 344
Availability: No items available.
|
|
1325.
|
|
|
1326.
|
|
|
1327.
|
Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan. [electronic resource] by
- Matsumoto, Hiroshi
- Hayashi, Yukiko K
- Kim, Dae-Son
- Ogawa, Megumu
- Murakami, Terumi
- Noguchi, Satoru
- Nonaka, Ikuya
- Nakazawa, Tomoyuki
- Matsuo, Takiko
- Futagami, Satoshi
- Campbell, Kevin P
- Nishino, Ichizo
Producer: 20050617
In:
Neuromuscular disorders : NMD vol. 15
Availability: No items available.
|
|
1328.
|
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy. [electronic resource] by
- Barone, Rita
- Aiello, Chiara
- Race, Valérie
- Morava, Eva
- Foulquier, Francois
- Riemersma, Moniek
- Passarelli, Chiara
- Concolino, Daniela
- Carella, Massimo
- Santorelli, Filippo
- Vleugels, Wendy
- Mercuri, Eugenio
- Garozzo, Domenico
- Sturiale, Luisa
- Messina, Sonia
- Jaeken, Jaak
- Fiumara, Agata
- Wevers, Ron A
- Bertini, Enrico
- Matthijs, Gert
- Lefeber, Dirk J
Producer: 20130103
In:
Annals of neurology vol. 72
Availability: No items available.
|
|
1329.
|
|
|
1330.
|
|
|
1331.
|
Genetic and microbial factors modulating the ubiquitin proteasome system in inflammatory bowel disease. [electronic resource] by
- Cleynen, Isabelle
- Vazeille, Emilie
- Artieda, Marta
- Verspaget, Hein W
- Szczypiorska, Magdalena
- Bringer, Marie-Agnès
- Lakatos, Peter L
- Seibold, Frank
- Parnell, Kirstie
- Weersma, Rinse K
- Mahachie John, Jestinah M
- Morgan-Walsh, Rebecca
- Staelens, Dominiek
- Arijs, Ingrid
- De Hertogh, Gert
- Müller, Stefan
- Tordai, Atilla
- Hommes, Daniel W
- Ahmad, Tariq
- Wijmenga, Cisca
- Pender, Sylvia
- Rutgeerts, Paul
- Van Steen, Kristel
- Lottaz, Daniel
- Vermeire, Severine
- Darfeuille-Michaud, Arlette
Producer: 20140909
In:
Gut vol. 63
Availability: No items available.
|
|
1332.
|
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. [electronic resource] by
- Dinçer, P
- Leturcq, F
- Richard, I
- Piccolo, F
- Yalnizoglu, D
- de Toma, C
- Akçören, Z
- Broux, O
- Deburgrave, N
- Brenguier, L
- Roudaut, C
- Urtizberea, J A
- Jung, D
- Tan, E
- Jeanpierre, M
- Campbell, K P
- Kaplan, J C
- Beckmann, J S
- Topaloglu, H
Producer: 19970905
In:
Annals of neurology vol. 42
Availability: No items available.
|
|
1333.
|
|
|
1334.
|
|
|
1335.
|
|
|
1336.
|
|
|
1337.
|
|
|
1338.
|
POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations. [electronic resource] by
- Di Costanzo, Stefania
- Balasubramanian, Anuradha
- Pond, Heather L
- Rozkalne, Anete
- Pantaleoni, Chiara
- Saredi, Simona
- Gupta, Vandana A
- Sunu, Christine M
- Yu, Timothy W
- Kang, Peter B
- Salih, Mustafa A
- Mora, Marina
- Gussoni, Emanuela
- Walsh, Christopher A
- Manzini, M Chiara
Producer: 20150610
In:
Human molecular genetics vol. 23
Availability: No items available.
|
|
1339.
|
|
|
1340.
|
|