עקוב אחר
Frank Baas
Frank Baas
LUMC
כתובת אימייל מאומתת בדומיין lumc.nl
כותרת
צוטט על ידי
צוטט על ידי
שנה
Analysis of expression of cMOAT (MRP2), MRP3, MRP4, and MRP5, homologues of the multidrug resistance-associated protein gene (MRP1), in human cancer cell lines
M Kool, M de Haas, GL Scheffer, RJ Scheper, MJT van Eijk, JA Juijn, ...
Cancer research 57 (16), 3537-3547, 1997
11811997
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ...
Science 347 (6229), 1436-1441, 2015
10382015
The human transcriptome map: clustering of highly expressed genes in chromosomal domains
H Caron, B Schaik, M Mee, F Baas, G Riggins, P Sluis, MC Hermus, ...
Science 291 (5507), 1289-1292, 2001
9672001
The human multidrug resistance-associated protein MRP is a plasma membrane drug-efflux pump
GJ Zaman, MJ Flens, MR Van Leusden, M De Haas, HS Mülder, ...
Proceedings of the National Academy of Sciences 91 (19), 8822-8826, 1994
8961994
MRP3, an organic anion transporter able to transport anti-cancer drugs
M Kool, M Van Der Linden, M de Haas, GL Scheffer, JML De Vree, ...
Proceedings of the National Academy of Sciences 96 (12), 6914-6919, 1999
8321999
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)
A Muchir, G Bonne, AJ van der Kooi, M van Meegen, F Baas, PA Bolhuis, ...
Human molecular genetics 9 (9), 1453-1459, 2000
7672000
Duplication in chromosome 17p11. 2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)
P Raeymaekers, V Timmerman, E Nelis, P De Jonghe, JE Hoogenduk, ...
Neuromuscular disorders 1 (2), 93-97, 1991
7551991
Mutations in ABCC6 cause pseudoxanthoma elasticum
AAB Bergen, AS Plomp, EJ Schuurman, S Terry, M Breuning, ...
Nature genetics 25 (2), 228, 2000
7082000
A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin‐Johnson syndrome
CC Paulusma, M Kool, PJ Bosma, GL Scheffer, F ter Borg, RJ Scheper, ...
Hepatology 25 (6), 1539-1542, 1997
7061997
The unfolded protein response is activated in Alzheimer’s disease
JJM Hoozemans, R Veerhuis, ES Van Haastert, JM Rozemuller, F Baas, ...
Acta neuropathologica 110, 165-172, 2005
6562005
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
6472018
Role of glutathione in the export of compounds from cells by the multidrug-resistance-associated protein.
GJ Zaman, J Lankelma, O vAN Tellingen, J Beijnen, H Dekker, ...
Proceedings of the National Academy of Sciences 92 (17), 7690-7694, 1995
6461995
Inactivating Mutations in the Gene for Thyroid Oxidase 2 (THOX2) and Congenital Hypothyroidism
JC Moreno, H Bikker, MJE Kempers, ASP Van Trotsenburg, F Baas, ...
New England Journal of Medicine 347 (2), 95-102, 2002
6332002
Multidrug-resistance protein 5 is a multispecific organic anion transporter able to transport nucleotide analogs
J Wijnholds, CAAM Mol, L van Deemter, M de Haas, GL Scheffer, F Baas, ...
Proceedings of the National Academy of Sciences 97 (13), 7476-7481, 2000
6092000
Abnormal heart rate and body temperature in mice lacking thyroid hormone receptor α1
L Wikström, C Johansson, C Saltó, C Barlow, AC Barros, F Baas, ...
The EMBO journal 17 (2), 455-461, 1998
5761998
Drug export activity of the human canalicular multispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA.
R Evers, M Kool, L van Deemter, H Janssen, J Calafat, LCJM Oomen, ...
The Journal of clinical investigation 101 (7), 1310-1319, 1998
5731998
Identical point mutations of PMP–22 in Trembler–J mouse and Charcot–Marie–Tooth disease type 1A
LJ Valentijn, F Baas, RA Wolterman, JE Hoogendijk, NHA van den Bosch, ...
Nature genetics 2 (4), 288-291, 1992
5081992
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13. 2–21.3
C Vance, A Al-Chalabi, D Ruddy, BN Smith, X Hu, J Sreedharan, ...
Brain 129 (4), 868-876, 2006
5072006
Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells
JCT Van Deutekom, M Bremmer-Bout, AAM Janson, IB Ginjaar, F Baas, ...
Human molecular genetics 10 (15), 1547-1554, 2001
5002001
N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy–Lom
L Kalaydjieva, D Gresham, R Gooding, L Heather, F Baas, R De Jonge, ...
The American Journal of Human Genetics 67 (1), 47-58, 2000
4892000
המערכת אינה יכולה לבצע את הפעולה כעת. נסה שוב מאוחר יותר.
מאמרים 1–20