Pascal Bernard

Melbourne, VIC 3010, Australia

Last Updated: 09/26/2026

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Found 14 publications

A long non-coding RNA Leat1 mediates the hormone responsiveness of EfnB2 during male urogenital development.

A long non-coding RNA Leat1 mediates the hormone responsiveness of EfnB2 during male urogenital development.

Journal: Research square

Published: July 18, 2023

A long non-coding RNA Leat1 mediates the hormone responsiveness of EfnB2 during male urogenital development.

A long non-coding RNA Leat1 mediates the hormone responsiveness of EfnB2 during male urogenital development.

Journal: Communications biology

Published: June 22, 2023

Oestrogen Activates the MAP3K1 Cascade and β-Catenin to Promote Granulosa-like Cell Fate in a Human Testis-Derived Cell Line.

Oestrogen Activates the MAP3K1 Cascade and β-Catenin to Promote Granulosa-like Cell Fate in a Human Testis-Derived Cell Line.

Journal: International journal of molecular sciences

Published: April 15, 2021

The inner ear proteome of fish.

The inner ear proteome of fish.

Journal: The FEBS journal

Published: September 02, 2018

Does transcription play a role in creating a condensin binding site?

Does transcription play a role in creating a condensin binding site?

Journal: Transcription

Published: January 31, 2015

Marker genes identify three somatic cell types in the fetal mouse ovary.

Marker genes identify three somatic cell types in the fetal mouse ovary.

Journal: Developmental biology

Published: June 27, 2014

RNA processing factors Swd2.2 and Sen1 antagonize RNA Pol III-dependent transcription and the localization of condensin at Pol III genes.

RNA processing factors Swd2.2 and Sen1 antagonize RNA Pol III-dependent transcription and the localization of condensin at Pol III genes.

Journal: PLoS genetics

Published: May 22, 2014

CPF-associated phosphatase activity opposes condensin-mediated chromosome condensation.

CPF-associated phosphatase activity opposes condensin-mediated chromosome condensation.

Journal: PLoS genetics

Published: December 18, 2013

Loss of function mutation in the palmitoyl-transferase HHAT leads to syndromic 46,XY disorder of sex development by impeding Hedgehog protein palmitoylation and signaling.

Loss of function mutation in the palmitoyl-transferase HHAT leads to syndromic 46,XY disorder of sex development by impeding Hedgehog protein palmitoylation and signaling.

Journal: PLoS genetics

Published: November 08, 2013

A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation.

A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutation.

Journal: PloS one

Published: March 22, 2012

Excess DAX1 leads to XY ovotesticular disorder of sex development (DSD) in mice by inhibiting steroidogenic factor-1 (SF1) activation of the testis enhancer of SRY-box-9 (Sox9).

Excess DAX1 leads to XY ovotesticular disorder of sex development (DSD) in mice by inhibiting steroidogenic factor-1 (SF1) activation of the testis enhancer of SRY-box-9 (Sox9).

Journal: Endocrinology

Published: February 02, 2012

Sox9 gene regulation and the loss of the XY/XX sex-determining mechanism in the mole vole Ellobius lutescens.

Sox9 gene regulation and the loss of the XY/XX sex-determining mechanism in the mole vole Ellobius lutescens.

Journal: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology

Published: January 05, 2012

Showing 1-12 of 14

Last Updated: 09/26/2026