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The Journal of Rheumatology
|
October 13, 2009
Is E148Q a benign polymorphism or a disease-causing mutation?
Dina Marek-Yagel, Ifat Bar-Joseph, Elon Pras, et al.
International Journal of Oncology
|
January 5, 2006
Estradiol and nicotine exposure enhances A549 bronchioloalveolar carcinoma xenograft growth in mice through the stimulation of angiogenesis
Michael J Jarzynka, Ping Guo, Ifat Bar-Joseph, et al.
Haematologica
|
October 13, 2022
Defective binding of ETS1 and STAT4 due to a mutation in the promoter region of <i>THPO</i> as a novel mechanism of congenital amegakaryocytic thrombocytopenia
Valeria Capaci, Etai Adam, Ifat Bar-Joseph, et al.
The Journal of Biological Chemistry
|
September 26, 2003
Altered fatty acid composition of dopaminergic neurons expressing alpha-synuclein and human brains with alpha-synucleinopathies
Ronit Sharon, Ifat Bar-Joseph, Gudrun E Mirick, et al.
Neuron
|
February 25, 2003
The formation of highly soluble oligomers of alpha-synuclein is regulated by fatty acids and enhanced in Parkinson's disease
Ronit Sharon, Ifat Bar-Joseph, Matthew P Frosch, et al.
Cancer Research
|
May 8, 2007
Angiopoietin-2 stimulates breast cancer metastasis through the alpha(5)beta(1) integrin-mediated pathway
Yorihisha Imanishi, Bo Hu, Michael J Jarzynka, et al.
Arthritis Care & Research
|
May 28, 2010
Role of the R92Q TNFRSF1A mutation in patients with familial Mediterranean fever
Dina Marek-Yagel, Yackov Berkun, Shai Padeh, et al.
Cancer Research
|
August 3, 2007
ELMO1 and Dock180, a bipartite Rac1 guanine nucleotide exchange factor, promote human glioma cell invasion
Michael J Jarzynka, Bo Hu, Kwok-Min Hui, et al.
European Journal of Medical Genetics
|
November 19, 2021
Broadening the phenotype of LRRK1 mutations - Features of malignant osteopetrosis and optic nerve atrophy with intrafamilial variable expressivity
Odelia Chorin, Guy Chowers, Rawan Agbariah, et al.
Human Genetics
|
July 25, 2012
Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia
Ifat Bar-joseph, Elon Pras, Haike Reznik-Wolf, et al.
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of 2
Search research articles
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Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
The Journal of Rheumatology
|
October 13, 2009
Is E148Q a benign polymorphism or a disease-causing mutation?
Dina Marek-Yagel, Ifat Bar-Joseph, Elon Pras, et al.
International Journal of Oncology
|
January 5, 2006
Estradiol and nicotine exposure enhances A549 bronchioloalveolar carcinoma xenograft growth in mice through the stimulation of angiogenesis
Michael J Jarzynka, Ping Guo, Ifat Bar-Joseph, et al.
Haematologica
|
October 13, 2022
Defective binding of ETS1 and STAT4 due to a mutation in the promoter region of <i>THPO</i> as a novel mechanism of congenital amegakaryocytic thrombocytopenia
Valeria Capaci, Etai Adam, Ifat Bar-Joseph, et al.
The Journal of Biological Chemistry
|
September 26, 2003
Altered fatty acid composition of dopaminergic neurons expressing alpha-synuclein and human brains with alpha-synucleinopathies
Ronit Sharon, Ifat Bar-Joseph, Gudrun E Mirick, et al.
Neuron
|
February 25, 2003
The formation of highly soluble oligomers of alpha-synuclein is regulated by fatty acids and enhanced in Parkinson's disease
Ronit Sharon, Ifat Bar-Joseph, Matthew P Frosch, et al.
Cancer Research
|
May 8, 2007
Angiopoietin-2 stimulates breast cancer metastasis through the alpha(5)beta(1) integrin-mediated pathway
Yorihisha Imanishi, Bo Hu, Michael J Jarzynka, et al.
Arthritis Care & Research
|
May 28, 2010
Role of the R92Q TNFRSF1A mutation in patients with familial Mediterranean fever
Dina Marek-Yagel, Yackov Berkun, Shai Padeh, et al.
Cancer Research
|
August 3, 2007
ELMO1 and Dock180, a bipartite Rac1 guanine nucleotide exchange factor, promote human glioma cell invasion
Michael J Jarzynka, Bo Hu, Kwok-Min Hui, et al.
European Journal of Medical Genetics
|
November 19, 2021
Broadening the phenotype of LRRK1 mutations - Features of malignant osteopetrosis and optic nerve atrophy with intrafamilial variable expressivity
Odelia Chorin, Guy Chowers, Rawan Agbariah, et al.
Human Genetics
|
July 25, 2012
Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia
Ifat Bar-joseph, Elon Pras, Haike Reznik-Wolf, et al.
Page
of 2