What Is Special about the “Human” in “Human Genetics”?

Por Nussbaum, Robert L.
Publicado em 2005

Mining yeast in silico unearths a golden nugget for mitochondrial biology

Por Nussbaum, Robert L.
Publicado em 2005

A tribute to Richard S. Spielman

Por Nussbaum, Robert L.
Publicado em 2009

The Identification of Alpha-Synuclein as the First Parkinson Disease Gene

Por Nussbaum, Robert L.
Publicado no J Parkinsons Dis (2017)

The Deficiency of PIP(2) 5-Phosphatase in Lowe Syndrome Affects Actin Polymerization

Por Suchy, Sharon F., Nussbaum, Robert L.
Publicado em 2002

X-inactivation analysis of embryonic lethality in Ocrl(wt/−);Inpp5b(−/−) mice

Por Bernard, David J., Nussbaum, Robert L.
Publicado em 2010

Prolongation of chemically-induced methemoglobinemia in mice lacking α-synuclein: A novel pharmacologic and toxicologic phenotype

Por Kuo, Yien-Ming, Nussbaum, Robert L.
Publicado no Toxicol Rep (2015)

A Case of Myocardial Infarction in a Patient with Werner's Syndrome

Por Soto-Figueroa, S. Fernando, Nussbaum, Robert L., Garcia, Efrain
Publicado em 1984

Thompson & Thompson genética médica /

Por Nussbaum, Robert L., McInnes, Roderick R., Willard, Huntington.
Publicado em 2008.

Prevalence of Parkinson's disease in populations of African ancestry: a review.

Por McInerney-Leo, Aideen, Gwinn-Hardy, Katrina, Nussbaum, Robert L.
Publicado em 2004

A single nucleotide polymorphism in the 3′UTR of the SNCA gene encoding alpha-synuclein is a new potential susceptibility locus for Parkinson disease

Por Sotiriou, Sotiria, Gibney, Gretchen, Baxevanis, Andreas D., Nussbaum, Robert L.
Publicado em 2009

Species-specific difference in expression and splice-site choice in Inpp5b, an inositol polyphosphate 5-phosphatase paralogous to the enzyme deficient in Lowe Syndrome

Por Bothwell, Susan P., Farber, Leslie W., Hoagland, Adam, Nussbaum, Robert L.
Publicado em 2010

Augmentation of phenotype in a transgenic Parkinson mouse heterozygous for a Gaucher mutation

Por Fishbein, Ianai, Kuo, Yien-Ming, Giasson, Benoit I., Nussbaum, Robert L.
Publicado no Brain (2014)

Regulation of α-Synuclein Expression by Poly (ADP Ribose) Polymerase-1 (PARP-1) Binding to the NACP-Rep1 Polymorphic Site Upstream of the SNCA Gene

Por Chiba-Falek, Ornit, Kowalak, Jeffrey A., Smulson, Mark E., Nussbaum, Robert L.
Publicado em 2005

Proteomics Analysis Identifies Phosphorylation-dependent α-Synuclein Protein Interactions

Por McFarland, Melinda A., Ellis, Christopher E., Markey, Sanford P., Nussbaum, Robert L.
Publicado em 2008

Deficiency in the p110α subunit of PI3K results in diminished Tie2 expression and Tie2(-/-)–like vascular defects in mice

Por Lelievre, Etienne, Bourbon, Pierre-Marie, Duan, Li-Juan, Nussbaum, Robert L., Fong, Guo-Hua
Publicado em 2005

Mitochondrial translocation of α-synuclein is promoted by intracellular acidification

Por Cole, Nelson B., DiEuliis, Diane, Leo, Paul, Mitchell, Drake C., Nussbaum, Robert L.
Publicado em 2008

Genetic Testing Before Anticoagulation? A Systematic Review of Pharmacogenetic Dosing of Warfarin

Por Kangelaris, Kirsten Neudoerffer, Bent, Stephen, Nussbaum, Robert L., Garcia, David A., Tice, Jeffrey A.
Publicado em 2009

Genetic Testing Before Anticoagulation? A Systematic Review of Pharmacogenetic Dosing of Warfarin

Por Kangelaris, Kirsten Neudoerffer, Bent, Stephen, Nussbaum, Robert L., Garcia, David A., Tice, Jeffrey A.
Publicado em 2009

Transgenic mice expressing S129 phosphorylation mutations in α-synuclein

Por Escobar, Valerie Drews, Kuo, Yien-Ming, Orrison, Bonnie M., Giasson, Benoit I., Nussbaum, Robert L.
Publicado em 2014