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Transformation-associated recombination (TAR) cloning for genomics studies and synthetic biology

Chromosoma, 2016-09, Vol.125 (4), p.621-632

2016

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Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome

American journal of human genetics, 2018-02, Vol.102 (2), p.296-308

2018

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Contribution of mGluR5 to pathophysiology in a mouse model of human chromosome 16p11.2 microdeletion

Nature neuroscience, 2015-02, Vol.18 (2), p.182-184

2015

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Pharmacological enhancement of mGlu5 receptors rescues behavioral deficits in SHANK3 knock-out mice

Molecular psychiatry, 2017-05, Vol.22 (5), p.689-702

2017

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Mild reproductive impact of a Y chromosome deletion on a C57BL/6J substrain

Mammalian genome, 2017-06, Vol.28 (5-6), p.155-165

2017

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Lipid Nanoparticle Formulation Increases Efficiency of DNA-Vectored Vaccines/Immunoprophylaxis in Animals Including Transchromosomic Bovines

Scientific reports, 2020-05, Vol.10 (1), p.8764, Article 8764

2020

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Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition

PLoS genetics, 2017-07, Vol.13 (7), p.e1006886-e1006886

2017

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Rescue of Sly Expression Is Not Sufficient to Rescue Spermiogenic Phenotype of Mice with Deletions of Y Chromosome Long Arm

Genes, 2019-02, Vol.10 (2), p.133

2019

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Comprehensive analysis of two Shank3 and the Cacna1c mouse models of autism spectrum disorder

Genes, brain and behavior, 2018-01, Vol.17 (1), p.4-22

2018

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Male‐specific alterations in structure of isolation call sequences of mouse pups with 16p11.2 deletion

Genes, brain and behavior, 2020-09, Vol.19 (7), p.e12681-n/a

2020

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An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions

PloS one, 2013-02, Vol.8 (2), p.e57460

2013

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15q13.3 homozygous knockout mouse model display epilepsy-, autism- and schizophrenia-related phenotypes

Translational psychiatry, 2016-07, Vol.6 (7), p.e860-e860

2016

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Decreased exploratory activity in a mouse model of 15q duplication syndrome; implications for disturbance of serotonin signaling

PloS one, 2010-12, Vol.5 (12), p.e15126-e15126

2010

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Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex

Proceedings of the National Academy of Sciences - PNAS, 2011-03, Vol.108 (11), p.4447-4452

2011

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Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficits

Communications biology, 2021-12, Vol.4 (1), p.1411-1411, Article 1411

2021

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Ts1Cje Down syndrome model mice exhibit environmental stimuli-triggered locomotor hyperactivity and sociability concurrent with increased flux through central dopamine and serotonin metabolism

Experimental neurology, 2017-07, Vol.293, p.1-12

2017

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Deletion of PREPl causes growth impairment and hypotonia in mice

PloS one, 2014-02, Vol.9 (2), p.e89160

2014

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Genetic and hormonal control of bone volume, architecture, and remodeling in XXY mice

Journal of bone and mineral research, 2010-10, Vol.25 (10), p.2148-2154

2010

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Restrained Phosphatidylcholine Synthesis in a Cellular Model of Down’s Syndrome is Associated with the Overexpression of Dyrk1A

Molecular neurobiology, 2017-03, Vol.54 (2), p.1092-1100

2017

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Congenital Heart Disease Revealing Familial 22q11 Deletion Syndrome

International journal of cardiovascular sciences, 2020-07, Vol.33 (4), p.425-426

2020

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A Zebrafish Model of 5q-Syndrome Using CRISPR/Cas9 Targeting RPS14 Reveals a p53-Independent and p53-Dependent Mechanism of Erythroid Failure

Journal of genetics and genomics, 2016-05, Vol.43 (5), p.307-318

2016

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Anatomy of trisomy 18

Clinical anatomy (New York, N.Y.), 2016-07, Vol.29 (5), p.628-632

2016

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Diagnostics and Prognostication of Myelodysplastic Syndromes

Annals of Laboratory Medicine, 2017, 37(6), , pp.465-474

Zini, Gina

2017

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Increased prostaglandin E₂-EP2 signalling in cumulus cells of female mice sired by males with the Y-chromosome long-arm deletion

Reproduction fertility and development, 2013, Vol.25 (6), p.900

2013

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Mijelodisplastični sindrom – nove spoznaje i „stara“ morfologija

Liječnički vjesnik, 2019-09, Vol.141 (7-8), p.209

2019

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Transformation-associated recombination (TAR) cloning for genomics studies and synthetic biology

Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome

Contribution of mGluR5 to pathophysiology in a mouse model of human chromosome 16p11.2 microdeletion

Pharmacological enhancement of mGlu5 receptors rescues behavioral deficits in SHANK3 knock-out mice

Mild reproductive impact of a Y chromosome deletion on a C57BL/6J substrain

Lipid Nanoparticle Formulation Increases Efficiency of DNA-Vectored Vaccines/Immunoprophylaxis in Animals Including Transchromosomic Bovines

Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition

Rescue of Sly Expression Is Not Sufficient to Rescue Spermiogenic Phenotype of Mice with Deletions of Y Chromosome Long Arm

Comprehensive analysis of two Shank3 and the Cacna1c mouse models of autism spectrum disorder

Male‐specific alterations in structure of isolation call sequences of mouse pups with 16p11.2 deletion

An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions

15q13.3 homozygous knockout mouse model display epilepsy-, autism- and schizophrenia-related phenotypes

Decreased exploratory activity in a mouse model of 15q duplication syndrome; implications for disturbance of serotonin signaling

Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex

Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficits

Ts1Cje Down syndrome model mice exhibit environmental stimuli-triggered locomotor hyperactivity and sociability concurrent with increased flux through central dopamine and serotonin metabolism

Deletion of PREPl causes growth impairment and hypotonia in mice

Genetic and hormonal control of bone volume, architecture, and remodeling in XXY mice

Restrained Phosphatidylcholine Synthesis in a Cellular Model of Down’s Syndrome is Associated with the Overexpression of Dyrk1A

Congenital Heart Disease Revealing Familial 22q11 Deletion Syndrome

A Zebrafish Model of 5q-Syndrome Using CRISPR/Cas9 Targeting RPS14 Reveals a p53-Independent and p53-Dependent Mechanism of Erythroid Failure

Anatomy of trisomy 18

Diagnostics and Prognostication of Myelodysplastic Syndromes

Increased prostaglandin E₂-EP2 signalling in cumulus cells of female mice sired by males with the Y-chromosome long-arm deletion

Mijelodisplastični sindrom – nove spoznaje i „stara“ morfologija

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