G. Brodsky

发表

A novel mutation in PLP1 causes severe hereditary spastic paraplegia type 2.

L. Noetzli, P. Sanz, G. Brodsky, 2014, Gene.

Sources of Variability in Platelet Accumulation on Type 1 Fibrillar Collagen in Microfluidic Flow Assays

Andrew T. Irish, Keith B. Neeves, G. Brodsky, 2013, PloS one.

Current perspective new insights into the molecular basis of familial dilated cardiomyopathy.

L. Mestroni, F. Muntoni, A. di Lenarda, 2001, Italian heart journal : official journal of the Italian Federation of Cardiology.

The human GARS-AIRS-GART gene encodes two proteins which are differentially expressed during human brain development and temporally overexpressed in cerebellum of individuals with Down syndrome.

G. Brodsky, D. Patterson, T. Barnes, 1997, Human molecular genetics.

Peptides derived from MARCKS block coagulation complex assembly on phosphatidylserine

H. Yin, L. Brass, G. Brodsky, 2017, Scientific Reports.

Development of a mouse model for the study of human purine metabolism.

G. Brodsky, D. Patterson, T. Barnes, 1994, Advances in experimental medicine and biology.

Epidemiology of cardiac actin gene mutations in dilated cardiomyopathy

L. Mestroni, M. B. Perryman, G. Brodsky, 1999 .

Hypoplastic left heart syndrome myocytes are differentiated but possess a unique phenotype.

M. B. Perryman, S. Helmke, G. Brodsky, 2003, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.

A novel transgenic mouse model of CBS-deficient homocystinuria does not incur hepatic steatosis or fibrosis and exhibits a hypercoagulative phenotype that is ameliorated by betaine treatment

L. Meltesen, R. Rozen, G. Brodsky, 2010, Molecular genetics and metabolism.

Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice

L. Reinholdt, R. Westrick, K. Tomberg, 2016, PloS one.

Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement.

L. Mestroni, F. Muntoni, G. Sinagra, 2000, Circulation.

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.

L. Mestroni, F. Muntoni, P. Fain, 2003, Journal of the American College of Cardiology.

A hyper-recombination mutation in S. cerevisiae identifies a novel eukaryotic topoisomerase

J. Wallis, G. Chrebet, R. Rothstein, 1989, Cell.

Constitutive induction of pro-inflammatory and chemotactic cytokines in cystathionine beta-synthase deficient homocystinuria.

G. Brodsky, J. V. Van Hove, D. Graham, 2011, Molecular genetics and metabolism.

The ENTPD1 promoter polymorphism −860 A > G (rs3814159) is associated with increased gene transcription, protein expression, CD39/NTPDase1 enzymatic activity, and thromboembolism risk

K. Moreau, C. Aquilante, U. Broeckel, 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Localization of STCH to human chromosome 21q11.1.

F. Kaye, G. Otterson, G. Brodsky, 1995, Genomics.

Mutations in the Chinese hamster ovary cell GART gene of de novo purine synthesis.

G. Brodsky, D. Patterson, A. Knox, 2009, Gene.

The prelamin A pre-peptide induces cardiac and skeletal myoblast differentiation.

G. Brodsky, K. Maclean, L. Miller, 2007, Biochemical and biophysical research communications.

The ENTPD1 promoter polymorphism −860 A > G (rs3814159) is associated with increased gene transcription, protein expression, CD39/NTPDase1 enzymatic activity, and thromboembolism risk

K. Moreau, C. Aquilante, U. Broeckel, 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Mutations in the Chinese hamster ovary cell GART gene of de novo purine synthesis.

G. Brodsky, D. Patterson, A. Knox, 2009, Gene.