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Obesity Research|April 24, 2001
The adipose tissue phenotype of hormone-sensitive lipase deficiency in miceS P Wang, N Laurin, J Himms-Hagen, et al.
Blood|February 1, 1997
Granulocyte-colony stimulating factor (filgrastim) accelerates granulocyte recovery after intensive postremission chemotherapy for acute myeloid leukemia with aziridinyl benzoquinone and mitoxantrone: Cancer and Leukemia Group B study 9022J O Moore, R K Dodge, P C Amrein, et al.
The Journal of Biological Chemistry|February 15, 1992
Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequencesL C Brody, G A Mitchell, C Obie, et al.
Brain Structure & Function|May 24, 2014
An analysis of von Economo neurons in the cerebral cortex of cetaceans, artiodactyls, and perissodactylsMary Ann Raghanti, Linda B Spurlock, F Robert Treichler, et al.
Applied and Environmental Microbiology|February 17, 2009
Ecophysiology of "Halarsenatibacter silvermanii" strain SLAS-1T, gen. nov., sp. nov., a facultative chemoautotrophic arsenate respirer from salt-saturated Searles Lake, CaliforniaJodi Switzer Blum, Sukkyun Han, Brian Lanoil, et al.
Veterinary Microbiology|December 26, 2012
Pre-infection of pigs with Mycoplasma hyopneumoniae induces oxidative stress that influences outcomes of a subsequent infection with a swine influenza virus of H1N1 subtypeC Deblanc, F Robert, T Pinard, et al.
Biochemistry|August 29, 2019
Structural Perturbations of Rhodopseudomonas palustris Form II RuBisCO Mutant Enzymes That Affect CO2 FixationSriram Satagopan, Justin A North, Mark A Arbing, et al.
Cancer|January 1, 1982
Radiation therapy with or without primary limited surgery for operable breast cancer: a 20-year experience at the Marseilles Cancer InstituteR Amalric, F Santamaria, F Robert, et al.
Investigational New Drugs|November 1, 1992
A phase II trial of CI-921 in advanced malignanciesN T Sklarin, P H Wiernik, W R Grove, et al.
American Journal of Human Genetics|April 16, 1998
HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41QG A Mitchell, P T Ozand, M F Robert, et al.
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