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Deletion of SREBF1, a Functional Bone-Muscle Pleiotropic Gene, Alters Bone Density and Lipid Signaling in Zebrafish

Endocrinology (Philadelphia), 2021-01, Vol.162 (1), p.1

2021

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Lrp5 Mutant and Crispant Zebrafish Faithfully Model Human Osteoporosis, Establishing the Zebrafish as a Platform for CRISPR‐Based Functional Screening of Osteoporosis Candidate Genes

Journal of bone and mineral research, 2021-09, Vol.36 (9), p.1749-1764

2021

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Interleukin 7 and thymic stromal lymphopoietin: from immunity to leukemia

Cellular and molecular life sciences : CMLS, 2014-02, Vol.71 (3), p.365-378

2014

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Beneficial Effect of Vitamin D on Non-Alcoholic Fatty Liver Disease (NAFLD) Progression in the Zebrafish Model

Nutrients, 2023-03, Vol.15 (6), p.1362

2023

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Role of hydrolyzed collagen in bone regeneration of adult zebrafish

Bone Reports, 2020-10, Vol.13, p.100411, Article 100411

2020

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NGLY1 Deficiency Zebrafish Model Manifests Abnormalities of the Nervous and Musculoskeletal Systems

Frontiers in cell and developmental biology, 2022-06, Vol.10, p.902969-902969

2022

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Zebrafish mutants reveal unexpected role of Lrp5 in osteoclast regulation

Frontiers in endocrinology (Lausanne), 2022-09, Vol.13, p.985304-985304

2022

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Membrane palmitoylated protein 7 (MPP7) and anaphase promoting complex subunit 1 (ANAPC1) associate with bone remodelling and osteoporosis

Bone Reports, 2020-10, Vol.13, p.100653, Article 100653

2020

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Lrp5 mutant and crispant zebrafish faithfully model human osteoporosis, establishing the zebrafish as a platform for CRISPR-based functional screening of osteoporosis candidate genes

Bone Reports, 2021-04, Vol.14, p.100836, Article 100836

2021

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Lrp5 gene knockout causes craniofacial deformities and fractures in adult zebrafish

Bone Reports, 2021-04, Vol.14, p.101047, Article 101047

2021

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Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis

Communications biology, 2023-07, Vol.6 (1), p.691-691, Article 691

2023

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Evaluation of the long-term skeletal effect induced by teratogen 5-aza-2′deoxycytidine on offspring of high (C3H/HeJ) and low (C57BL/6J) bone mass phenotype mice

Bone Reports, 2018-06, Vol.8, p.239-243

2018

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A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer

BMC cancer, 2007, Vol.7 (1), p.14-14, Article 14

2007

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Gain-of-function mutations in interleukin-7 receptor-α (IL7R) in childhood acute lymphoblastic leukemias

The Journal of experimental medicine, 2011-05, Vol.208 (5), p.901-908

2011

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Lugol as a chemical enabler of enhanced imaging for bone-muscle tissues in fish model

Bone Reports, 2022-05, Vol.16, p.101448, Article 101448

2022

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Towards precision medicine in childhood leukemia – Insights from mutationally activated cytokine receptor pathways in acute lymphoblastic leukemia

Cancer letters, 2014-09, Vol.352 (1), p.15-20

2014

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Compensatory Mechanisms In Mouse Offspring With Inherently Weak Bones Are Suggesting A Gene‐By‐Environment Interaction In Utero

The FASEB journal, 2015-04, Vol.29 (S1)

2015

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Mutation spectrum in HNPCC in the Israeli population

Familial cancer, 2008-12, Vol.7 (4), p.309-317

2008

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Targeting oncogenic interleukin‐7 receptor signalling with N‐acetylcysteine in T cell acute lymphoblastic leukaemia

British journal of haematology, 2015-01, Vol.168 (2), p.230-238

2015

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Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients From Different Ethnic Groups of the Israeli Population

American journal of ophthalmology, 2011-02, Vol.151 (2), p.263-271.e1

2011

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Gain-of-function mutations in interleukin-7 receptor -α ( IL7R ) in childhood acute lymphoblastic leukemias

The Journal of experimental medicine, 2011-06, Vol.208 (6), p.1333-1333

2011

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Evaluation of the long-term skeletal effect induced by teratogen 5-aza-2'deoxycytidine on offspring of high (C3H/HeJ) and low (C57BL/6J) bone mass phenotype mice

Bone Reports, 2018-06, Vol.8, p.239-243

2018

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A protocol for genetic evaluation of patients with multiple colorectal adenomas and without evidence of APC gene mutation

The Israel Medical Association journal, 2010-09, Vol.12 (9), p.549-553

2010

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Deletion of SREBF1, a Functional Bone-Muscle Pleiotropic Gene, Alters Bone Density and Lipid Signaling in Zebrafish

Lrp5 Mutant and Crispant Zebrafish Faithfully Model Human Osteoporosis, Establishing the Zebrafish as a Platform for CRISPR‐Based Functional Screening of Osteoporosis Candidate Genes

Interleukin 7 and thymic stromal lymphopoietin: from immunity to leukemia

Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome

Beneficial Effect of Vitamin D on Non-Alcoholic Fatty Liver Disease (NAFLD) Progression in the Zebrafish Model

Role of hydrolyzed collagen in bone regeneration of adult zebrafish

NGLY1 Deficiency Zebrafish Model Manifests Abnormalities of the Nervous and Musculoskeletal Systems

Zebrafish mutants reveal unexpected role of Lrp5 in osteoclast regulation

Membrane palmitoylated protein 7 (MPP7) and anaphase promoting complex subunit 1 (ANAPC1) associate with bone remodelling and osteoporosis

Lrp5 mutant and crispant zebrafish faithfully model human osteoporosis, establishing the zebrafish as a platform for CRISPR-based functional screening of osteoporosis candidate genes

Lrp5 gene knockout causes craniofacial deformities and fractures in adult zebrafish

Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis

Evaluation of the long-term skeletal effect induced by teratogen 5-aza-2′deoxycytidine on offspring of high (C3H/HeJ) and low (C57BL/6J) bone mass phenotype mice

A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer

Gain-of-function mutations in interleukin-7 receptor-α (IL7R) in childhood acute lymphoblastic leukemias

Lugol as a chemical enabler of enhanced imaging for bone-muscle tissues in fish model

Towards precision medicine in childhood leukemia – Insights from mutationally activated cytokine receptor pathways in acute lymphoblastic leukemia

Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group

Compensatory Mechanisms In Mouse Offspring With Inherently Weak Bones Are Suggesting A Gene‐By‐Environment Interaction In Utero

Mutation spectrum in HNPCC in the Israeli population

Targeting oncogenic interleukin‐7 receptor signalling with N‐acetylcysteine in T cell acute lymphoblastic leukaemia

Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients From Different Ethnic Groups of the Israeli Population

Gain-of-function mutations in interleukin-7 receptor -α ( IL7R ) in childhood acute lymphoblastic leukemias

Evaluation of the long-term skeletal effect induced by teratogen 5-aza-2'deoxycytidine on offspring of high (C3H/HeJ) and low (C57BL/6J) bone mass phenotype mice

A protocol for genetic evaluation of patients with multiple colorectal adenomas and without evidence of APC gene mutation

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