A new class of histone H2A mutations in Saccharomyces cerevisiae causes specific transcriptional defects in vivo.

Por Hirschhorn, J N, Bortvin, A L, Ricupero-Hovasse, S L, Winston, F
Publicado em 1995

A new trinuclear complex of platinum and iron efficiently promotes cleavage of plasmid DNA.

Por Lempers, E L, Bashkin, J S, Kostić, N M
Publicado em 1993

Functional interaction between GCN5 and polyamines: a new role for core histone acetylation.

Por Pollard, K J, Samuels, M L, Crowley, K A, Hansen, J C, Peterson, C L
Publicado em 1999

Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease

Por Blok, M J, Spruijt, L, de Coo, I F M, Schoonderwoerd, K, Hendrickx, A, Smeets, H J
Publicado em 2007

Characterisation of a new alpha thalassemia 1 defect due to a partial deletion of the alpha globin gene complex.

Por Pressley, L, Higgs, D R, Aldridge, B, Metaxatou-Mavromati, A, Clegg, J B, Weatherall, D J
Publicado em 1980

Novel fungal genera and species associated with the sooty blotch and flyspeck complex on apple in China and the USA

Por Yang, H.L., Sun, G.Y., Batzer, J.C., Crous, P.W., Groenewald, J.Z., Gleason, M.L.
Publicado em 2010

Incubation of MDCO-216 (ApoA-IMilano/POPC) with Human Serum Potentiates ABCA1-Mediated Cholesterol Efflux Capacity, Generates New Prebeta-1 HDL, and Causes an Increase in HDL Size

Por Kempen, Herman J., Schranz, Dorota B., Asztalos, Bela F., Otvos, James, Jeyarajah, Elias, Drazul-Schrader, Denise, Collins, Heidi L., Adelman, Steven J., Wijngaard, Peter L. J.
Publicado no J Lipids (2014)

Incubation of MDCO-216 (ApoA-IMilano/POPC) with Human Serum Potentiates ABCA1-Mediated Cholesterol Efflux Capacity, Generates New Prebeta-1 HDL, and Causes an Increase in HDL Size

Por Herman J. Kempen, Dorota B. Schranz, Bela F. Asztalos, James Otvos, Elias Jeyarajah, Denise Drazul-Schrader, Heidi L. Collins, Steven J. Adelman, Peter L. J. Wijngaard
Publicado em 2014-01-01

An ancient revisits cosmology.

Por Greenstein, J L
Publicado em 1993

Identification and characterization of ten new water gaps in seeds and fruits with physical dormancy and classification of water-gap complexes

Por Gama-Arachchige, N. S., Baskin, J. M., Geneve, R. L., Baskin, C. C.
Publicado em 2013

New developments in the treatment of hypoactive sexual desire disorder – a focus on Flibanserin

Por Jayne, Christopher J, Heard, Michael J, Zubair, Sarah, Johnson, Dustie L
Publicado no Int J Womens Health (2017)

New frontiers in neuroimaging applications to inborn errors of metabolism

Por Prust, Morgan J., Gropman, Andrea L., Hauser, Natalie
Publicado em 2011

Investigating the Potential Influence of Cause of Death and Cocaine Levels on the Differential Expression of Genes Associated with Cocaine Abuse

Por Bannon, Michael J., Savonen, Candace L., Hartley, Zachary J., Johnson, Magen M., Schmidt, Carl J.
Publicado no PLoS One (2015)

Complex patterns of linkage disequilibrium in the Huntington disease region.

Por MacDonald, M E, Lin, C, Srinidhi, L, Bates, G, Altherr, M, Whaley, W L, Lehrach, H, Wasmuth, J, Gusella, J F
Publicado em 1991

Haploinsufficiency for Core Exon Junction Complex Components Disrupts Embryonic Neurogenesis and Causes p53-Mediated Microcephaly

Por Mao, Hanqian, McMahon, John J., Tsai, Yi-Hsuan, Wang, Zefeng, Silver, Debra L.
Publicado no PLoS Genet (2016)

Dynamic light scattering study of calmodulin-target peptide complexes.

Por Papish, Andriyka L, Tari, Leslie W, Vogel, Hans J
Publicado em 2002

Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome

Por Gerards, M, Sluiter, W, van den Bosch, B J C, de Wit, L E A, Calis, C M H, Frentzen, M, Akbari, H, Schoonderwoerd, K, Scholte, H R, Jongbloed, R J, Hendrickx, A T M, de Coo, I F M, Smeets, H J M
Publicado em 2009

Late outcome of Senning and Mustard procedures for correction of transposition of the great arteries

Por Dos, L, Teruel, L, Ferreira, I J, Rodriguez-Larrea, J, Miro, L, Girona, J, Albert, D C, Gonçalves, A, Murtra, M, Casaldaliga, J
Publicado em 2005

E2 transacylase-deficient (type II) maple syrup urine disease. Aberrant splicing of E2 mRNA caused...

Por Chuang, J L, Cox, R P, Chuang, D T
Publicado em 1997

Mycobacterium arupense, Mycobacterium heraklionense, and a Newly Proposed Species, “Mycobacterium virginiense” sp. nov., but Not Mycobacterium nonchromogenicum, as Species of the Mycobacterium terrae Complex...

Por Vasireddy, Ravikiran, Vasireddy, Sruthi, Brown-Elliott, Barbara A., Wengenack, Nancy L., Eke, Uzoamaka A., Benwill, Jeana L., Turenne, Christine, Wallace, Richard J.
Publicado no J Clin Microbiol (2016)