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861.
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862.
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Induced pluripotent stem cell models of progranulin-deficient frontotemporal dementia uncover specific reversible neuronal defects. [electronic resource] by
- Almeida, Sandra
- Zhang, Zhijun
- Coppola, Giovanni
- Mao, Wenjie
- Futai, Kensuke
- Karydas, Anna
- Geschwind, Michael D
- Tartaglia, M Carmela
- Gao, Fuying
- Gianni, Davide
- Sena-Esteves, Miguel
- Geschwind, Daniel H
- Miller, Bruce L
- Farese, Robert V
- Gao, Fen-Biao
Producer: 20130326
In:
Cell reports vol. 2
Availability: No items available.
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863.
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Association Between Progranulin and Gaucher Disease. [electronic resource] by
- Jian, Jinlong
- Zhao, Shuai
- Tian, Qing-Yun
- Liu, Helen
- Zhao, Yunpeng
- Chen, Wen-Chi
- Grunig, Gabriele
- Torres, Paola A
- Wang, Betty C
- Zeng, Bai
- Pastores, Gregory
- Tang, Wei
- Sun, Ying
- Grabowski, Gregory A
- Kong, Max Xiangtian
- Wang, Guilin
- Chen, Ying
- Liang, Fengxia
- Overkleeft, Herman S
- Saunders-Pullman, Rachel
- Chan, Gerald L
- Liu, Chuan-Ju
Producer: 20170214
In:
EBioMedicine vol. 11
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864.
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865.
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PGRN acts as a novel regulator of mitochondrial homeostasis by facilitating mitophagy and mitochondrial biogenesis to prevent podocyte injury in diabetic nephropathy. [electronic resource] by
- Zhou, Di
- Zhou, Meng
- Wang, Ziying
- Fu, Yi
- Jia, Meng
- Wang, Xiaojie
- Liu, Min
- Zhang, Yan
- Sun, Yu
- Lu, Yi
- Tang, Wei
- Yi, Fan
Producer: 20200706
In:
Cell death & disease vol. 10
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866.
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867.
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868.
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869.
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Predicting functional decline in behavioural variant frontotemporal dementia. [electronic resource] by
- Josephs, Keith A
- Whitwell, Jennifer L
- Weigand, Stephen D
- Senjem, Matthew L
- Boeve, Bradley F
- Knopman, David S
- Smith, Glenn E
- Ivnik, Robert J
- Jack, Clifford R
- Petersen, Ronald C
Producer: 20110411
In:
Brain : a journal of neurology vol. 134
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870.
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871.
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Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulin. [electronic resource] by
- McDade, E
- Boeve, B F
- Burrus, T M
- Boot, B P
- Kantarci, K
- Fields, J
- Lowe, V J
- Peller, P
- Knopman, D
- Baker, M
- Finch, N
- Rademakers, R
- Petersen, R
Producer: 20120612
In:
Neurology vol. 78
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872.
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873.
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Nocturnal levels of chemerin and progranulin in adolescents: influence of sex, body mass index, glucose metabolism and sleep. [electronic resource] by
- Daxer, Johann
- Herttrich, Theresa
- Zhao, Ying Y
- Vogel, Mandy
- Hiemisch, Andreas
- Scheuermann, Kathrin
- Körner, Antje
- Kratzsch, Jürgen
- Kiess, Wieland
- Quante, Mirja
Producer: 20170508
In:
Journal of pediatric endocrinology & metabolism : JPEM vol. 30
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874.
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875.
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876.
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"Frontotemporoparietal" dementia: clinical phenotype associated with the c.709-1G>A PGRN mutation. [electronic resource] by
- Moreno, F
- Indakoetxea, B
- Barandiaran, M
- Alzualde, A
- Gabilondo, A
- Estanga, A
- Ruiz, J
- Ruibal, M
- Bergareche, A
- Martí-Massó, J F
- López de Munain, A
Producer: 20091202
In:
Neurology vol. 73
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877.
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Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia. [electronic resource] by
- van der Zee, Julie
- Le Ber, Isabelle
- Maurer-Stroh, Sebastian
- Engelborghs, Sebastiaan
- Gijselinck, Ilse
- Camuzat, Agnès
- Brouwers, Nathalie
- Vandenberghe, Rik
- Sleegers, Kristel
- Hannequin, Didier
- Dermaut, Bart
- Schymkowitz, Joost
- Campion, Dominique
- Santens, Patrick
- Martin, Jean-Jacques
- Lacomblez, Lucette
- De Pooter, Tim
- Peeters, Karin
- Mattheijssens, Maria
- Vercelletto, Martine
- Van den Broeck, Marleen
- Cruts, Marc
- De Deyn, Peter P
- Rousseau, Frederic
- Brice, Alexis
- Van Broeckhoven, Christine
Producer: 20070501
In:
Human mutation vol. 28
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878.
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Progranulin genetic variability contributes to amyotrophic lateral sclerosis. [electronic resource] by
- Sleegers, K
- Brouwers, N
- Maurer-Stroh, S
- van Es, M A
- Van Damme, P
- van Vught, P W J
- van der Zee, J
- Serneels, S
- De Pooter, T
- Van den Broeck, M
- Cruts, M
- Schymkowitz, J
- De Jonghe, P
- Rousseau, F
- van den Berg, L H
- Robberecht, W
- Van Broeckhoven, C
Producer: 20080902
In:
Neurology vol. 71
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879.
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880.
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Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation. [electronic resource] by
- Suárez-Calvet, Marc
- Dols-Icardo, Oriol
- Lladó, Albert
- Sánchez-Valle, Raquel
- Hernández, Isabel
- Amer, Guillermo
- Antón-Aguirre, Sofía
- Alcolea, Daniel
- Fortea, Juan
- Ferrer, Isidre
- van der Zee, Julie
- Dillen, Lubina
- Van Broeckhoven, Christine
- Molinuevo, José Luís
- Blesa, Rafael
- Clarimón, Jordi
- Lleó, Alberto
Producer: 20140620
In:
Journal of neurology, neurosurgery, and psychiatry vol. 85
Availability: No items available.
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