M. Brusel

发表

Type I procollagen COOH-terminal proteinase enhancer protein: identification, primary structure, and chromosomal localization of the cognate human gene (PCOLCE).

R. Eddy, T. Shows, D. Greenspan, 1994, The Journal of biological chemistry.

Bone Morphogenetic Protein-1: The Type I Procollagen C-Proteinase

D. Greenspan, E. Kessler, K. Takahara, 1996, Science.

Bone Morphogenetic Protein-1 (BMP-1) Mediates C-terminal Processing of Procollagen V Homotrimer*

E. Kessler, M. Brusel, F. Ruggiero, 2001, The Journal of Biological Chemistry.

COL1 C‐propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta

T. Hefferan, M. Yaszemski, A. Boskey, 2011, Human mutation.

Exogenous NaV1.1 activity in excitatory and inhibitory neurons reverts Dravet syndrome comorbidities when delivered post-symptom onset in mice with Dravet

Ethan M. Goldberg, M. Rubinstein, E. Kremer, 2022, bioRxiv.

Detection of Duchenne muscular dystrophy gene products in amniotic fluid and chorionic villus sampling cells

M. Brusel, U. Nudel, D. Yaffe, 1993 .

COL1A1 C-propeptide mutations cause ER mislocalization of procollagen and impair C-terminal procollagen processing.

D. Eyre, S. Leikin, A. Ashok, 2019, Biochimica et biophysica acta. Molecular basis of disease.

Quasi-Elastic (p, px) Reactions on Lithium and Carbon at 156 MeV

M. Bernas, M. Sowiński, M. Brusel, 1970 .

Heat-induced seizures, premature mortality, and hyperactivity in a novel Scn1a nonsense model for Dravet syndrome

V. Dani, M. Rubinstein, M. Brusel, 2023, bioRxiv.

The NTR domain of procollagen C-proteinase enhancer-1 (PCPE-1) mediates PCPE-1 binding to syndecans-1, -2 and -4 as well as fibronectin.

E. Kessler, M. Brusel, T. Weiss, 2014, The international journal of biochemistry & cell biology.

Functional Investigation of a Neuronal Microcircuit in the CA1 Area of the Hippocampus Reveals Synaptic Dysfunction in Dravet Syndrome Mice

M. Rubinstein, M. Brusel, Y. Almog, 2022, Frontiers in Molecular Neuroscience.

Developmental alterations in firing properties of hippocampal CA1 inhibitory and excitatory neurons in a mouse model of Dravet syndrome

M. Rubinstein, M. Brusel, Y. Almog, 2020, Neurobiology of Disease.

In vivo, in vitro and in silico correlations of four de novo SCN1A missense mutations

M. Rubinstein, B. Ben-Zeev, M. Brusel, 2019, PloS one.

Early hippocampal hyperexcitability followed by disinhibition in a mouse model of Dravet syndrome

M. Brusel, Y. Almog, K. Anderson, 2019, bioRxiv.

Acute effect of antiseizure drugs on background oscillations in Scn1a A1783V Dravet syndrome mouse model

M. Brusel, Shir Quinn, Mor Ovadia, 2022, bioRxiv.