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A. Moser

Nature Genetics, Biochimica et Biophysica Acta, Annals of Neurology, Proceedings of the National Academy of Sciences of the United States of America, Hepatology, Transplantation, Journal of Neuropathology and Experimental Neurology Show more
12
Role
Title
Level Year L/R
🐜 Probiotics and antibodies to TNF inhibit inflammatory activity and improve nonalcoholic fatty liver disease
9 auth. Zhiping Li, Shiqi Yang, Huizhi Lin, Jiawen Huang, P. Watkins, A. Moser, ... C. Desimone, Xiao-yu Song, A. Diehl 		9 2003
9
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🐒 Functions of plasmalogen lipids in health and disease.
N. Braverman, A. Moser 		9 2012
9
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🐜 Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
8 auth. G. Dodt, N. Braverman, Candice C. Wong, A. Moser, H. Moser, P. Watkins, ... D. Valle, S. Gould 		8 1995
8
🐜
🐜 Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata
7 auth. N. Braverman, G. Steel, C. Obie, A. Moser, H. Moser, S. Gould, ... D. Valle 		8 1997
8
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🐜 Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening
8 auth. L. Bezman, A. Moser, G. Raymond, P. Rinaldo, P. Watkins, Kirby D. Smith, ... Nancy E. Kass, H. Moser 		8 2001
8
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🦁 Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls
7 auth. A. Moser, N. Kreiter, L. Bezman, Shou‐En Lu, G. Raymond, S. Naidu, ... H. Moser 		8 1999
8
🦁
🐬 Peroxisome biogenesis disorders.
S. Steinberg, G. Dodt, G. Raymond, N. Braverman, A. Moser, H. Moser 		8 2006
8
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🐬 Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.
B. Migeon, H. Moser, A. Moser, J. Axelman, D. Sillence, R. Norum 		8 1981
8
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🐜 A mouse model for X-linked adrenoleukodystrophy.
8 auth. Jyh-Feng Lu, A. Lawler, P. Watkins, J. Powers, A. Moser, H. Moser, ... H. Moser, Klrby D. Smith 		8 1997
8
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🐜 Hepatocyte transplantation in a 4-year-old girl with peroxisomal biogenesis disease: technique, safety, and metabolic follow-up.
12 auth. E. Sokal, F. Smets, A. Bourgois, L. Van Maldergem, J. Buts, R. Reding, ... Jean Bernard Otte, V. Evrard, D. Latinne, M. Vincent, A. Moser, H. Soriano 		8 2003
8
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🐬 The Inflammatory Myelinopathy of Adreno‐Leukodystrophy: Cells, Effector Molecules, and Pathogenetic Implications
J. Powers, Yan Liu, A. Moser, H. Moser 		8 1992
8
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🐜 Mutations in the gene encoding 3Ξ²-hydroxysteroid-Ξ” 8,Ξ”7-isomerase cause X-linked dominant Conradi-HΓΌnermann syndrome
12 auth. N. Braverman, P. Lin, F. F. Moebius, C. Obie, A. Moser, H. Glossmann, ... W. Wilcox, D. Rimoin, Moyra J. Smith, L. Kratz, R. Kelley, D. Valle 		7 1999
7
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