Commentary

Por Olson, Timothy S., Bessler, Monica
Publicado em 2013

Human K(ATP) channelopathies: diseases of metabolic homeostasis

Por Olson, Timothy M., Terzic, Andre
Publicado em 2009

CXCR2- and E-Selectin–induced Neutrophil Arrest during Inflammation In Vivo

Por Smith, Michael L., Olson, Timothy S., Ley, Klaus
Publicado em 2004

Acquired Aplastic Anemia in Children

Por Hartung, Helge D., Olson, Timothy S., Bessler, Monica
Publicado em 2013

Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia

Por Babushok, Daria V., Olson, Timothy S., Bessler, Monica
Publicado no N Engl J Med (2015)

Genetic predisposition to myelodysplastic syndrome and acute myeloid leukemia in children and young adults

Por Babushok, Daria V., Bessler, Monica, Olson, Timothy S.
Publicado no Leuk Lymphoma (2015)

Recent advances in understanding clonal haematopoiesis in aplastic anaemia

Por Stanley, Natasha, Olson, Timothy S., Babushok, Daria V.
Publicado no Br J Haematol (2017)

X-Linked Nonsyndromic Sinus Node Dysfunction and Atrial Fibrillation Caused by Emerin Mutation

Por KARST, MARGARET L., HERRON, KATHLEEN J., OLSON, TIMOTHY M.
Publicado em 2008

Comprehensive Mutation Scanning of LMNA in 268 Patients With Lone Atrial Fibrillation

Por Brauch, Katharine M., Chen, Lin Y., Olson, Timothy M.
Publicado em 2009

Exome Sequencing Establishes Diagnosis of Alström Syndrome in an Infant Presenting with Non-Syndromic Dilated Cardiomyopathy

Por Long, Pamela A., Evans, Jared M., Olson, Timothy M.
Publicado no Am J Med Genet A (2015)

Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy

Por Long, Pamela A., Larsen, Brandon T., Evans, Jared M., Olson, Timothy M.
Publicado no J Am Heart Assoc (2015)

Lone Atrial Fibrillation: Influence of Familial Disease on Gender Predilection

Por CHEN, LIN Y., HERRON, KATHLEEN J., TAI, BEE C., OLSON, TIMOTHY M.
Publicado em 2008

Advances in Cardiac ATP-Sensitive K(+) Channelopathies From Molecules to Populations

Por Terzic, Andre, Alekseev, Alexey E., Yamada, Satsuki, Reyes, Santiago, Olson, Timothy M.
Publicado em 2011

K(ATP) channel Kir6.2 E23K variant overrepresented in human heart failure is associated with impaired exercise stress response

Por Reyes, Santiago, Park, Sungjo, Johnson, Bruce D., Terzic, Andre, Olson, Timothy M.
Publicado em 2009

Cardiac K(ATP) channels in health and disease

Por Kane, Garvan C., Liu, Xiao-Ke, Yamada, Satsuki, Olson, Timothy M., Terzic, Andre
Publicado em 2005

Mice with a Mutation in the Mdm2 Gene That Interferes with MDM2/Ribosomal Protein Binding Develop a Defect in Erythropoiesis

Por Kamio, Takuya, Gu, Bai-wei, Olson, Timothy S., Zhang, Yanping, Mason, Philip J., Bessler, Monica
Publicado no PLoS One (2016)

Histoplasmosis infection in patients with rheumatoid arthritis, 1998-2009

Por Olson, Timothy C, Bongartz, Tim, Crowson, Cynthia S, Roberts, Glenn D, Orenstein, Robert, Matteson, Eric L
Publicado em 2011

Genomes or exomes: evaluation of cost, time and coverage

Por Middha, Sumit, Theis, Jeanne L, Goodloe, Adele H, Olson, Timothy M, Kocher, Jean-Pierre A
Publicado em 2011

De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy

Por Long, Pamela A., Zimmermann, Michael T., Kim, Maengjo, Evans, Jared M., Xu, Xiaolei, Olson, Timothy M.
Publicado no Hum Genet (2016)

K(ATP) channel polymorphism is associated with left ventricular size in hypertensive individuals: a large-scale community-based study

Por Reyes, Santiago, Terzic, Andre, Mahoney, Douglas W., Redfield, Margaret M., Rodeheffer, Richard J., Olson, Timothy M.
Publicado em 2008