28 results on '"Rahmani, Zohra"'
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2. Erratum: Dulac et al., “A Novel Neuron-Specific Regulator of the V-ATPase inDrosophila”
3. Separating the Spindle, Checkpoint, and Timer Functions of BubR1
4. Critical Role of the D21S55 Region on Chromosome 21 in the Pathogenesis of Down Syndrome
5. A Novel Neuron-Specific Regulator of the V-ATPase inDrosophila
6. aPKC‐mediated phosphorylation regulates asymmetric membrane localization of the cell fate determinant Numb
7. New Insights into the Role of BubR1 in Mitosis and Beyond
8. Partial physical map of human chromosome 21 from fibroblast and lymphocyte DNA
9. New chromosome 21 DNA markers isolated by pulsed field gel electrophoresis from an ETS2-containing Down syndrome chromosomal region
10. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
11. Superoxide Dismutase, Oxygen Radical Metabolism, and Amyotrophic Lateral Sclerosis
12. Overexpression of mSim2 gene in the zona limitans of the diencephalon of segmental trisomy 16 Ts1Cje fetuses, a mouse model for trisomy 21: a novel whole-mount based RNA hybridization study
13. A novel mutation in the N-terminal domain of Drosophila BubR1 affects the spindle assembly checkpoint function of BubR1
14. Chapter Six - New Insights into the Role of BubR1 in Mitosis and Beyond
15. Cenp-meta is required for sustained spindle checkpoint
16. A mitotic role for Mad1 beyond the spindle checkpoint
17. APRO4 negatively regulates Src tyrosine kinase activity in PC12 cells
18. DYRK1A Enhances the Mitogen-activated Protein Kinase Cascade in PC12 Cells by Forming a Complex with Ras, B-Raf, and MEK1
19. Down syndrome critical region around D21S55 on proximal 21q22.3
20. Dual-specificity tyrosine-phosphorylated and regulated kinase 1A (DYRK1A) interacts with the phytanoyl-CoA α-hydroxylase associated protein 1 (PAHX-AP1), a brain specific protein
21. Hepatitis B Virus X Protein Colocalizes to Mitochondria with a Human Voltage-Dependent Anion Channel, HVDAC3, and Alters Its Transmembrane Potential
22. Expression of the Mnb (dyrk) Protein in Adult and Embryonic Mouse Tissues
23. Isolation of a novel human voltage-dependent anion channel gene
24. A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis
25. Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21
26. Gene-dosage mapping of 30 DNA markers on chromosome 21
27. 3 - Superoxide Dismutase, Oxygen Radical Metabolism, and Amyotrophic Lateral Sclerosis
28. Etude du rôle et de la régulation de BubR1 dans la ségrégation des chromosomes acentriques
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