Ann B Moser
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Probiotics and antibodies to TNF inhibit inflammatory activity and improve nonalcoholic fatty liver disease
Z Li, S Yang, H Lin, J Huang, PA Watkins, AB Moser, C DeSimone, ...
Hepatology 37 (2), 343-350, 2003
Functions of plasmalogen lipids in health and disease
NE Braverman, AB Moser
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1822 (9 …, 2012
Peroxisome biogenesis disorders
SJ Steinberg, G Dodt, GV Raymond, NE Braverman, AB Moser, ...
Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1763 (12), 1733-1748, 2006
X-linked adrenoleukodystrophy
HW Moser, KD Smith, AB Moser
Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata
N Braverman, G Steel, C Obie, A Moser, H Moser, SJ Gould, D Valle
Nature genetics 15 (4), 369-376, 1997
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
G Dodt, N Braverman, C Wong, A Moser, HW Moser, P Watkins, D Valle, ...
Nature genetics 9 (2), 115-125, 1995
Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids
HW Moser, AB Moser, KK Frayer, W Chen, JD Schulman, BP O'Neill, ...
Neurology 51 (2), 334-334-a, 1998
Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening
L Bezman, AB Moser, GV Raymond, P Rinaldo, PA Watkins, KD Smith, ...
Annals of neurology 49 (4), 512-517, 2001
Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls
AB Moser, N Kreiter, L Bezman, SE Lu, GV Raymond, S Naidu, HW Moser
Annals of Neurology: Official Journal of the American Neurological …, 1999
Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.
BR Migeon, HW Moser, AB Moser, J Axelman, D Sillence, RA Norum
Proceedings of the National Academy of Sciences 78 (8), 5066-5070, 1981
A mouse model for X-linked adrenoleukodystrophy
JF Lu, AM Lawler, PA Watkins, JM Powers, AB Moser, HW Moser, ...
Proceedings of the National Academy of Sciences 94 (17), 9366-9371, 1997
Mutations in the gene encoding 3β-hydroxysteroid-Δ8, Δ7-isomerase cause X-linked dominant Conradi-Hünermann syndrome
N Braverman, P Lin, FF Moebius, C Obie, A Moser, H Glossmann, ...
Nature genetics 22 (3), 291-294, 1999
Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy
S Kemp, HM Wei, JF Lu, LT Braiterman, MC McGuinness, AB Moser, ...
Nature medicine 4 (11), 1261-1268, 1998
Follow-up of 89 asymptomatic patients with adrenoleukodystrophy treated with Lorenzo’s oil
HW Moser, GV Raymond, SE Lu, LR Muenz, AB Moser, J Xu, RO Jones, ...
Archives of neurology 62 (7), 1073-1080, 2005
The inflammatory myelinopathy of adreno-leukodystrophy: cells, effector molecules, and pathogenetic implications
JM Powers, Y Liu, AB Moser, HW Moser
Journal of Neuropathology & Experimental Neurology 51 (6), 630-643, 1992
Adrenoleukodystrophy: phenotypic variability and implications for therapy
HW Moser, AB Moser, KD Smith, A Bergin, J Borel, J Shankroff, OC Stine, ...
Journal of inherited metabolic disease 15 (4), 645-664, 1992
Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups
AB Moser, M Rasmussen, S Naidu, PA Watkins, M McGuinness, AK Hajra, ...
The Journal of pediatrics 127 (1), 13-22, 1995
Clinical and biochemical spectrum of patients with RSH/Smith‐Lemli‐Opitz syndrome and abnormal cholesterol metabolism
C Cunniff, LE Kratz, A Moser, MR Natowicz, RI Kelley
American journal of medical genetics 68 (3), 263-269, 1997
Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes
RI Kelley, NS Datta, WB Dobyns, AK Hajra, AB Moser, MJ Noetzel, ...
American journal of medical genetics 23 (4), 869-901, 1986
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines
NE Braverman, GV Raymond, WB Rizzo, AB Moser, ME Wilkinson, ...
Molecular genetics and metabolism 117 (3), 313-321, 2016
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