Z. Rahmani

发表

DYRK1A enhances the mitogen-activated protein kinase cascade in PC12 cells by forming a complex with Ras, B-Raf, and MEK1.

P. Kelly, Z. Rahmani, 2005, Molecular biology of the cell.

Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21

J. Delabar, Z. Rahmani, D. Theophile, 1993, European journal of human genetics : EJHG.

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

J. Haines, M. Pericak-Vance, H. Horvitz, 1993, Nature.

aPKC‐mediated phosphorylation regulates asymmetric membrane localization of the cell fate determinant Numb

P. Thibault, F. Schweisguth, G. Brothers, 2007, The EMBO journal.

Dual-specificity tyrosine-phosphorylated and regulated kinase 1A (DYRK1A) interacts with the phytanoyl-CoA alpha-hydroxylase associated protein 1 (PAHX-AP1), a brain specific protein.

Z. Rahmani, Marilyne Bescond, 2005, The international journal of biochemistry & cell biology.

Cenp-meta is required for sustained spindle checkpoint

R. Karess, Z. Rahmani, Thomas Rubin, 2014, Biology Open.

Superoxide dismutase, oxygen radical metabolism, and amyotrophic lateral sclerosis.

Z. Rahmani, D. Patterson, H. Warner, 1994, Molecular genetic medicine.

New chromosome 21 DNA markers isolated by pulsed field gel electrophoresis from an ETS2-containing Down syndrome chromosomal region

M. Yaspo, J. Delabar, Z. Rahmani, 1992, Human Genetics.

APRO4 negatively regulates Src tyrosine kinase activity in PC12 cells

Z. Rahmani, 2006, Journal of Cell Science.

APRO 4 negatively regulates Src tyrosine kinase activity in PC 12 cells

Z. Rahmani, 2022 .

Lamp1 Deficiency Enhances Sensitivity to α-Synuclein and Oxidative Stress in Drosophila Models of Parkinson Disease

S. Birman, Z. Rahmani, Satya Surabhi, 2022, International journal of molecular sciences.

Expression of the mnb (dyrk) protein in adult and embryonic mouse tissues.

J. Delabar, Z. Rahmani, M. Rachidi, 1998, Biochemical and biophysical research communications.

Hepatitis B Virus X Protein Colocalizes to Mitochondria with a Human Voltage-Dependent Anion Channel, HVDAC3, and Alters Its Transmembrane Potential

A. Siddiqui, Z. Rahmani, R. Lasher, 2000, Journal of Virology.

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

A. Aurias, J. Delabar, Z. Rahmani, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level.

J. Delabar, Z. Rahmani, D. Theophile, 1994, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

New insights into the role of BubR1 in mitosis and beyond.

R. Karess, Z. Rahmani, K. Wassmann, 2013, International review of cell and molecular biology.

A novel mutation in the N-terminal domain of Drosophila BubR1 affects the spindle assembly checkpoint function of BubR1

Z. Rahmani, J. Montagne, M. Duranteau, 2016, Biology Open.

A mitotic role for Mad1 beyond the spindle checkpoint

R. Karess, Z. Rahmani, R. Terracol, 2011, Journal of Cell Science.

Separating the spindle, checkpoint, and timer functions of BubR1

R. Karess, Z. Rahmani, C. Lefebvre, 2009, The Journal of cell biology.

Down syndrome: a model for the study of Alzheimer’s disease and aging

J. Delabar, Z. Rahmani, Z. Chettouh, 1990 .

Partial physical map of human chromosome 21 from fibroblast and lymphocyte DNA

M. Yaspo, J. Delabar, Z. Rahmani, 1993, Human Genetics.

Gene-dosage mapping of 30 DNA markers on chromosome 21.

D. Patterson, J. Delabar, Z. Rahmani, 1992, Genomics.

Down Syndrome Critical Region Around D 21 S 55 On Proximal 21 q 22 . 3

A. Aurias, J. Delabar, Z. Rahmani, 2005 .

Down syndrome critical region around D21S55 on proximal 21q22.3.

A. Aurias, Z. Rahmani, Z. Chettouh, 2005, American journal of medical genetics. Supplement.

Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21.

J. Fermanian, Z. Rahmani, Z. Chettouh, 1990, American journal of human genetics.

Isolation of a novel human voltage-dependent anion channel gene

A. Siddiqui, Z. Rahmani, C. Maunoury, 1998, European Journal of Human Genetics.

A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis.

H. Horvitz, T. Usdin, Z. Rahmani, 1994, Human molecular genetics.

Molecular mapping of the Down syndrome phenotype on chromosome 21.

J. Delabar, Z. Rahmani, D. Theophile, 1993, Progress in clinical and biological research.

Molecular Analysis of Patients with Alzheimer's Disease

J. Delabar, Y. Lamour, Z. Rahmani, 1988 .

Physical mapping of chromosome 21.

D. Patterson, Z. Rahmani, K. Gardiner, 1993, Progress in clinical and biological research.

Chromosome 21, Trisomy 21, and Alzheimer’s Disease

J. Delabar, J. Huret, Z. Rahmani, 1988 .

Separating the spindle, checkpoint, and timer functions of BubR1

R. Karess, Z. Rahmani, C. Lefebvre, 2009, The Journal of cell biology.