T. Potikha

发表

Galectin-1 is essential for efficient liver regeneration following hepatectomy

G. Rabinovich, E. Galun, O. Pappo, 2016, Oncotarget.

A novel splice‐site mutation in ECM‐1 gene in a consanguineous family with lipoid proteinosis

B. Glaser, A. Zlotogorski, L. Horev, 2005, Experimental dermatology.

The homozygous M712T mutation of UDP‐N‐acetylglucosamine 2‐epimerase/N‐acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy

K. Yarema, W. Reutter, S. Mitrani‐Rosenbaum, 2004, FEBS letters.

A mutant of Arabidopsis thaliana displaying altered patterns of cellulose deposition

D. Delmer, T. Potikha, 1995 .

Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair.

A. Tosti, A. Zlotogorski, L. Horev, 2009, Journal of the American Academy of Dermatology.

HCV Tumor Promoting Effect Is Dependent on Host Genetic Background

E. Galun, O. Pappo, D. Goldenberg, 2009, PloS one.

Lipoid proteinosis: identification of two novel mutations in the human ECM-1 gene and lack of genotype-phenotype correlation.

J. McGrath, A. Zlotogorski, L. Horev, 2009, Acta Dermato-Venereologica.

BjalphaIT: a novel scorpion alpha-toxin selective for insects--unique pharmacological tool.

M. Elazar, J. Tytgat, T. Arnon, 2005, Insect biochemistry and molecular biology.

p57Kip2 (cdkn1c): sequence, splice variants and unique temporal and spatial expression pattern in the rat pancreas

B. Glaser, T. Potikha, I. Ariel, 2005, Laboratory Investigation.

Interstrain differences in chronic hepatitis and tumor development in a murine model of inflammation‐mediated hepatocarcinogenesis

Evgeniy Stoyanov, Amnon Peled, Orit Pappo, 2013, Hepatology.

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Tsviya Olender, Doron Lancet, Jacques S. Beckmann, 2001, Nature Genetics.

Structures and functions of annexins in plants

D. Delmer, T. Potikha, 1997, Cellular and Molecular Life Sciences CMLS.

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.

A. Eliakim, B. Glaser, L. Aguilar-Bryan, 2004, The Journal of clinical endocrinology and metabolism.

Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13

C. L. Jackson, M. Shemesh, T. Levi, 2001, European Journal of Human Genetics.

BjαIT: a novel scorpion α-toxin selective for insects—unique pharmacological tool

M. Elazar, J. Tytgat, T. Arnon, 2005 .

Lack of galectin‐1 exacerbates chronic hepatitis, liver fibrosis, and carcinogenesis in murine hepatocellular carcinoma model

G. Rabinovich, E. Galun, O. Pappo, 2019, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

The involvement of hydrogen peroxide in the differentiation of secondary walls in cotton fibers

Levine, D. Delmer, A. Levine, 1999, Plant physiology.