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Identification of a Novel Hypoxia-Inducible Factor 1-Responsive Gene, RTP801, Involved in Apoptosis

Molecular and Cellular Biology, 2002-04, Vol.22 (7), p.2283-2293

2002

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Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease

American journal of human genetics, 1992-01, Vol.50 (1), p.222-228

1992

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Identification of a novel stress-responsive gene Hi95 involved in regulation of cell viability

Oncogene, 2002-09, Vol.21 (39), p.6017-6031

2002

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The Role of Organ Vascularization and Lipoplex-Serum Initial Contact in Intravenous Murine Lipofection

The Journal of biological chemistry, 2003-10, Vol.278 (41), p.39858-39865

2003

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Inhibition of Oxygen-Induced Retinopathy in RTP801-Deficient Mice

Investigative ophthalmology & visual science, 2004-10, Vol.45 (10), p.3796-3805

2004

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Similar levels of mRNA from the W1282X and the ΔF508 cystic fibrosis alleles, in nasal epithelial cells

The Journal of clinical investigation, 1994-04, Vol.93 (4), p.1502-1507

1994

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A New Mutation in the CFTR Gene, Composed of Two Adjacent DNA Alterations, Is a Common Cause of Cystic Fibrosis among Georgian Jews

Genomics (San Diego, Calif.), 1993, Vol.15 (1), p.236-237

1993

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trans activation of rat phosphoenolpyruvate carboxykinase (GTP) gene expression by micro-coinjection of rat liver mRNA in Xenopus laevis oocytes

Molecular and Cellular Biology, 1989-11, Vol.9 (11), p.5244-5247

1989

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Cystic fibrosis manifested as undescended testis and absence of vas deferens

Pediatrics (Evanston), 1992-12, Vol.90 (6), p.982-983

1992

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The Molecular Basis of Disease Variability among Cystic Fibrosis Patients Carrying the 3849+10 kb C→T Mutation

Genomics (San Diego, Calif.), 1998-11, Vol.53 (3), p.276-283

1998

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Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel

Human genetics, 1995-08, Vol.96 (2), p.193-197

1995

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Analysis of Random Recombination between Human MDR1 and Mouse Mdr1a cDNA in a pHaMDR-Dihydrofolate Reductase Bicistronic Expression System

Molecular pharmacology, 1998-10, Vol.54 (4), p.623-630

1998

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[34] pHaMDR-DHFR bicistronic expression system for mutational analysis of P-glycoprotein

Methods in Enzymology, 1998, Vol.292, p.474-480

1998

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Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010 delTATT in exon 21

Human molecular genetics, 1994, Vol.3 (4), p.657-658

1994

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The Molecular Basis of Disease Variability among Cystic Fibrosis Patients Carrying the 3849+10 kb C arrow right T Mutation

Genomics (San Diego, Calif.), 1998-11, Vol.53 (3), p.276-283

1998

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Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis

Human genetics, 1993-10, Vol.92 (3), p.289-295

1993

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Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010delTATT in exon 21

Human molecular genetics, 1994-04, Vol.3 (4), p.657-658

1994

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Cis -regulatory elements that confer differential expression upon the rat gene encoding phosphoenolpyruvate carboxykinase in kidney and liver

Gene, 1991-05, Vol.101 (2), p.279-283

1991

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Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic group in Israel

Human genetics, 1995, Vol.96 (2), p.193-197

1995

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Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentiation of severe disease

American journal of human genetics, 1992, Vol.50 (1), p.222-228

1992

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Cell specific expression of rat pepck gene in tissues form different embryonal origin

Cell differentiation and development, 1989-08, Vol.27, p.219-219

1989

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Elephants

The Encyclopedia of Mammals, 2006

3, 2006

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Turnover of purine nucleotides in rabbit erythrocytes. II. Studies in vitro

Biochimica et biophysica acta, 1967-11, Vol.149 (1), p.59

1967

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Turnover of purine nucleotides in rabbit erythrocytes I. Studies in vivo

Biochimica et biophysica acta, 1967-11, Vol.149 (1), p.50-58

1967

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The roots of compassion in early childhood: Relationships between theory of mind and attachment representations with empathic concern and prosocial behavior

Journal of experimental child psychology, 2024-06, Vol.242, p.105880-105880, Article 105880

Shoshani, Anat

2024

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Identification of a Novel Hypoxia-Inducible Factor 1-Responsive Gene, RTP801, Involved in Apoptosis

Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease

Identification of a novel stress-responsive gene Hi95 involved in regulation of cell viability

The Role of Organ Vascularization and Lipoplex-Serum Initial Contact in Intravenous Murine Lipofection

Inhibition of Oxygen-Induced Retinopathy in RTP801-Deficient Mice

Similar levels of mRNA from the W1282X and the ΔF508 cystic fibrosis alleles, in nasal epithelial cells

A New Mutation in the CFTR Gene, Composed of Two Adjacent DNA Alterations, Is a Common Cause of Cystic Fibrosis among Georgian Jews

trans activation of rat phosphoenolpyruvate carboxykinase (GTP) gene expression by micro-coinjection of rat liver mRNA in Xenopus laevis oocytes

Cystic fibrosis manifested as undescended testis and absence of vas deferens

The Molecular Basis of Disease Variability among Cystic Fibrosis Patients Carrying the 3849+10 kb C→T Mutation

Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel

Analysis of Random Recombination between Human MDR1 and Mouse Mdr1a cDNA in a pHaMDR-Dihydrofolate Reductase Bicistronic Expression System

[34] pHaMDR-DHFR bicistronic expression system for mutational analysis of P-glycoprotein

Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010 delTATT in exon 21

The Molecular Basis of Disease Variability among Cystic Fibrosis Patients Carrying the 3849+10 kb C arrow right T Mutation

Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis

Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010delTATT in exon 21

Cis -regulatory elements that confer differential expression upon the rat gene encoding phosphoenolpyruvate carboxykinase in kidney and liver

Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic group in Israel

Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentiation of severe disease

Cell specific expression of rat pepck gene in tissues form different embryonal origin

Elephants

Turnover of purine nucleotides in rabbit erythrocytes. II. Studies in vitro

Turnover of purine nucleotides in rabbit erythrocytes I. Studies in vivo

The roots of compassion in early childhood: Relationships between theory of mind and attachment representations with empathic concern and prosocial behavior

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