O. Ojarikre

发表

Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice

William Davies, D. Skuse, L. Wilkinson, 2005, Nature Genetics.

Deficiency in the Multicopy Sycp3-Like X-Linked Genes Slx and Slxl1 Causes Major Defects in Spermatid Differentiation

Peter J. I. Ellis, P. Burgoyne, N. Affara, 2010, Molecular biology of the cell.

Cardiovascular Development and Disease Preliminary Evidence for Aortopathy and an X-linked Parent-of-origin Effect on Aortic Valve Malformation in a Mouse Model of Turner Syndrome

L. Wilkinson, R. Hinton, W. Davies, 2022 .

Insights into regulation of the mammalian cell cycle from studies on spermatogenesis using genetic approaches in animal models

D. Elliott, J. Turner, A. Touré, 2004, Cytogenetic and Genome Research.

Identification of novel Y chromosome encoded transcripts by testis transcriptome analysis of mice with deletions of the Y chromosome long arm

K. Loveland, A. Touré, S. Mahadevaiah, 2005, Genome Biology.

Expression of peroxisomal proteins provides clear evidence for the presence of peroxisomes in the male germ cell line GC1spg

D. Elliott, J. Turner, A. Touré, 2004, Cytogenetic and Genome Research.

ATR is a multifunctional regulator of male mouse meiosis

Julian Lange, S. Keeney, D. D. de Rooij, 2018, Nature Communications.

The androgen receptor in spermatogenesis

D. Elliott, J. Turner, A. Touré, 2004, Cytogenetic and Genome Research.

Recombination between the mouse Y chromosome short arm and an additional Y short arm-derived chromosomal segment attached distal to the X chromosome PAR

M. Mitchell, Fanny Decarpentrie, P. Burgoyne, 2015, Chromosoma.

Steroid sulfatase-deficient mice exhibit endophenotypes relevant to Attention Deficit Hyperactivity Disorder

T. Humby, W. Davies, P. Burgoyne, 2012, Psychoneuroendocrinology.

Recombination between the mouse Y chromosome short arm and an additional Y short arm-derived chromosomal segment attached distal to the X chromosome PAR

M. Mitchell, Fanny Decarpentrie, P. Burgoyne, 2015, Chromosoma.

Live Offspring from Mice Lacking the Y Chromosome Long Arm Gene Complement1

P. Burgoyne, O. Ojarikre, Y. Yamauchi, 2009, Biology of reproduction.

A new deletion of the mouse Y chromosome long arm associated with the loss of Ssty expression, abnormal sperm development and sterility.

A. Touré, S. Mahadevaiah, P. Burgoyne, 2004, Genetics.

A protein encoded by a member of the multicopy Ssty gene family located on the long arm of the mouse Y chromosome is expressed during sperm development.

A. Touré, S. Mahadevaiah, P. Burgoyne, 2004, Genomics.

Does Rbmy have a role in sperm development in mice?

D. Elliott, J. Turner, A. Touré, 2003, Cytogenetic and Genome Research.

CRISPR-Cas9 effectors facilitate generation of single-sex litters and sex-specific phenotypes

Jasmin Zohren, James M. A. Turner, S. Mahadevaiah, 2021, Nature Communications.

Patterns, mechanisms, and functions of translation regulation in mammalian spermatogenic cells

D. Elliott, J. Turner, A. Touré, 2004, Cytogenetic and Genome Research.

Fertile offspring from sterile sex chromosome trisomic mice

H. Ohta, B. E. Powell, M. Saitou, 2017, Science.

Human and mouse ZFY genes produce a conserved testis-specific transcript encoding a zinc finger protein with a short acidic domain and modified transactivation potential

M. Mitchell, Eric Streichemberger, Fanny Decarpentrie, 2012, Human molecular genetics.

The expression of Y-linked Zfy2 in XY mouse oocytes leads to frequent meiosis 2 defects, a high incidence of subsequent early cleavage stage arrest and infertility

Fanny Decarpentrie, S. Mahadevaiah, Nadège Vernet, 2014, Development.

Synergistic effects of germ cell expressed genes on male fertility in mice

D. Elliott, J. Turner, A. Touré, 2004, Cytogenetic and Genome Research.

A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis

M. Mitchell, C. Bishop, S. Mahadevaiah, 2001, Nature Genetics.

The Y-Encoded Gene Zfy2 Acts to Remove Cells with Unpaired Chromosomes at the First Meiotic Metaphase in Male Mice

M. Mitchell, A. Bradley, H. Prosser, 2011, Current Biology.

Altered brain gene expression but not steroid biochemistry in a genetic mouse model of neurodevelopmental disorder

W. Davies, O. Ojarikre, Simon Trent, 2014, Molecular Autism.

Biological mechanisms associated with increased perseveration and hyperactivity in a genetic mouse model of neurodevelopmental disorder

T. Humby, G. Bedse, T. Cassano, 2013, Psychoneuroendocrinology.

The BCL-2 pathway preserves mammalian genome integrity by eliminating recombination-defective oocytes

K. Niakan, A. Mccarthy, D. Wells, 2020, Nature Communications.

SETDB1 Links the Meiotic DNA Damage Response to Sex Chromosome Silencing in Mice

K. Niakan, A. Snijders, D. D. de Rooij, 2018, Developmental cell.

Expression of the B56δ subunit of protein phosphatase 2A and Mea1 in mouse spermatogenesis. Identification of a new B56γ subunit (B56γ4) specifically expressed in testis

D. Elliott, J. Turner, A. Touré, 2004, Cytogenetic and Genome Research.

Non-Canonical and Sexually Dimorphic X Dosage Compensation States in the Mouse and Human Germline

Antoine H. F. M. Peters, Michael B. Stadler, A. Sesay, 2017, Developmental cell.

Evidence that postnatal growth retardation in XO mice is due to haploinsufficiency for a non-PAR X gene

J. Turner, P. Burgoyne, O. Ojarikre, 2003, Cytogenetic and Genome Research.

DNA damage response protein TOPBP1 regulates X chromosome silencing in the mammalian germ line

D. D. de Rooij, James M. A. Turner, E. Elinati, 2017, Proceedings of the National Academy of Sciences.

Genetic and Pharmacological Modulation of the Steroid Sulfatase Axis Improves Response Control; Comparison with Drugs Used in ADHD

L. Wilkinson, T. Humby, W. Davies, 2014, Neuropsychopharmacology.

Altered Serotonergic Function may Partially Account for Behavioral Endophenotypes in Steroid Sulfatase-deficient Mice

T. Humby, G. Bedse, T. Cassano, 2012, Neuropsychopharmacology.

Generating single-sex litters: development of CRISPR-Cas9 genetic tools to produce all-male offspring

Jasmin Zohren, James M. A. Turner, O. Ojarikre, 2020, bioRxiv.

ATR is a multifunctional regulator of male mouse meiosis

Julian Lange, S. Keeney, D. D. de Rooij, 2017, bioRxiv.

The BCL-2 pathway preserves mammalian genome integrity by eliminating recombination-defective oocytes

K. Niakan, A. Mccarthy, D. Wells, 2020, Nature Communications.

Deficiency in the Multicopy Sycp3-Like X-Linked Genes Slx and Slxl1 Causes Major Defects in Spermatid Differentiation

Peter J. I. Ellis, P. Burgoyne, N. Affara, 2010, Molecular biology of the cell.

ATR is a multifunctional regulator of male mouse meiosis

Julian Lange, S. Keeney, D. D. de Rooij, 2017, bioRxiv.

Steroid sulfatase-deficient mice exhibit endophenotypes relevant to Attention Deficit Hyperactivity Disorder

T. Humby, W. Davies, P. Burgoyne, 2012, Psychoneuroendocrinology.

Biological mechanisms associated with increased perseveration and hyperactivity in a genetic mouse model of neurodevelopmental disorder

T. Humby, T. Cassano, W. Davies, 2013, Psychoneuroendocrinology.

Determining the potency of primordial germ cells by injection into early mouse embryos.

Harry G. Leitch, James M. A. Turner, Nobuhiko Hamazaki, 2024, Developmental cell.