A. Galli

发表

High-throughput discovery of novel developmental phenotypes

Steve D. M. Brown, Lisa X. Yu, Jacqueline K. White, 2017 .

Human and mouse essentiality screens as a resource for disease gene discovery

Steve D. M. Brown, Jacqueline K. White, Ghina Bou About, 2020, Nature Communications.

Reduction of BMP4 activity by gremlin 1 enables ureteric bud outgrowth and GDNF/WNT11 feedback signalling during kidney branching morphogenesis

R. Zeller, J. Lopez-Rios, A. Galli, 2007, Development.

Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy

D. Adams, W. Weninger, A. Galli, 2014, Disease Models & Mechanisms.

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome

Michael E. Coulter, C. Walsh, S. Wiemann, 2017, Genome research.

The venous system of E14.5 mouse embryos—reference data and examples for diagnosing malformations in embryos with gene deletions

Jacqueline K. White, W. Weninger, A. Galli, 2021, Journal of anatomy.

Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21–S23

D. Adams, W. Weninger, A. Galli, 2017, Journal of anatomy.

Placentation defects are highly prevalent in embryonic lethal mouse mutants

Jacqueline K. White, D. Adams, J. Collins, 2018, Nature.

Common and distinct transcriptional signatures of mammalian embryonic lethality

Jacqueline K. White, D. Adams, I. Sealy, 2019, Nature Communications.

Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM)

Jacqueline K. White, W. Weninger, A. Galli, 2021, Biomedicines.

The Col4a2em1(IMPC)Wtsi mouse line: lessons from the Deciphering the Mechanisms of Developmental Disorders program

Jacqueline K. White, D. Adams, W. Weninger, 2019, Biology Open.

Corrigendum: High-throughput discovery of novel developmental phenotypes

Steve D. M. Brown, Jacqueline K. White, Mark W. Moore, 2017, Nature.

Differential regulation of gene expression in the digit forming area of the mouse limb bud by SHH and gremlin 1/FGF-mediated epithelial-mesenchymal signalling

R. Zeller, A. Zuniga, Nadège Lagarde, 2006, Development.

Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm

Steven J. M. Jones, D. Labuda, H. Dietz, 2014, Nature Genetics.

Rapid conversion of EUCOMM/KOMP-CSD alleles in mouse embryos using a cell-permeable Cre recombinase

R. Ramirez-Solis, E. Ryder, J. Bussell, 2013, Transgenic Research.

Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole‐body energy expenditure

Anneliese O. Speak, N. Karp, C. Lelliott, 2016, The Journal of pathology.

Regulation of extra-embryonic endoderm stem cell differentiation by Nodal and Cripto signaling

Mariano J. Alvarez, A. Califano, M. Alvarez, 2011, Development.

Detailed characterizations of cranial nerve anatomy in E14.5 mouse embryos/fetuses and their use as reference for diagnosing subtle, but potentially lethal malformations in mutants

A. Galli, T. Mohun, S. Geyer, 2022, Frontiers in Cell and Developmental Biology.

Characterization of Sgo1 expression in developing and adult mouse.

S. Nattel, G. Andelfinger, A. Galli, 2017, Gene expression patterns : GEP.

Human and mouse essentiality screens as a resource for disease gene discovery

Steve D. M. Brown, Jacqueline K. White, Denise G. Lanza, 2019, bioRxiv.

Rapid conversion of EUCOMM/KOMP-CSD alleles in mouse embryos using a cell-permeable Cre recombinase

R. Ramirez-Solis, E. Ryder, J. Bussell, 2013, Transgenic Research.

Activin/Nodal signaling and NANOG orchestrate human embryonic stem cell fate decisions by controlling the H3K4me3 chromatin mark

Antonella Galli, Ludovic Vallier, Pedro Madrigal, 2015, Genes & development.

Synthetic lethality between PAXX and XLF in mammalian development

Anneliese O. Speak, A. Speak, D. Adams, 2016, Genes & development.

Glypicans are differentially expressed during patterning and neurogenesis of early mouse brain.

S. Forlani, A. Galli, K. Lawson, 2007, Biochemical and biophysical research communications.

Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos

R. Zeller, A. Galli, A. Roure, 2003, Development.

Prevalence of sexual dimorphism in mammalian phenotypic traits

Steve D. M. Brown, Anneliese O. Speak, Jacqueline K. White, 2017, Nature Communications.

Genome-wide in vivo screen identifies novel host regulators of metastatic colonization

Edward Ryder, David J. Adams, Louise van der Weyden, 2017, Nature.

GLI3 constrains digit number by controlling both progenitor proliferation and BMP-dependent exit to chondrogenesis.

Rolf Zeller, Antonella Galli, Dario Speziale, 2012, Developmental cell.

Dual RMCE for efficient re-engineering of mouse mutant alleles

B. Rosen, R. Zeller, J. Lopez-Rios, 2010, Nature Methods.

Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation

B. Séraphin, V. Gladyshev, M. O'Donohue, 2019, PLoS genetics.

Glypicans and FGFs in CNS Development and Function

A. Galli, 2003 .

Distinct Roles of Hand2 in Initiating Polarity and Posterior Shh Expression during the Onset of Mouse Limb Bud Development

R. Paro, R. Zeller, S. Mackem, 2010, PLoS genetics.

PRMT5 is essential for the maintenance of chondrogenic progenitor cells in the limb bud

Hongkai Ji, S. Vokes, S. Mackem, 2016, Development.

Limb Pattern Formation

A. Zuniga, A. Galli, 2006 .

Targeting of NAT10 enhances healthspan in a mouse model of human accelerated aging syndrome

Jacqueline K. White, N. Karp, C. Lelliott, 2018, Nature Communications.

Mouse limb deformity mutations disrupt a global control region within the large regulatory landscape required for Gremlin expression.

D. Duboule, R. Zeller, A. Zuniga, 2004, Genes & development.

The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation

Damian Smedley, Paul Flicek, Steve D. M. Brown, 2018, Conservation Genetics.

Regulation of extra-embryonic endoderm stem cell differentiation by Nodal and Cripto signaling

A. Califano, M. Alvarez, M. Shen, 2011, Development.

PCR fingerprinting of whole genomes : the spacers between the 16 s and 23 s rRNA genes and of intergenic tRNA gene regions reveal a different intraspecific genomic variability of Bacillus cereus and Bacillus licheniforrnis

E. Zanardini, A. Galli, Galli, 2008 .

Highly variable penetrance of abnormal phenotypes in embryonic lethal knockout mice

R. Ramirez-Solis, D. Adams, W. Weninger, 2016, Mechanisms of Development.

Hypoglossal Nerve Abnormalities as Biomarkers for Central Nervous System Defects in Mouse Lines Producing Embryonically Lethal Offspring

W. Weninger, A. Galli, T. Mohun, 2021, Frontiers in Neuroanatomy.

FGF2 Signaling Is Required for the Development of Neuronal Circuits Regulating Blood Pressure

R. Zeller, A. Zuniga, H. Ehmke, 2002, Circulation research.

Visualising the Cardiovascular System of Embryos of Biomedical Model Organisms with High Resolution Episcopic Microscopy (HREM)

David J. Adams, Antonella Galli, Jacqueline K. White, 2018, Journal of cardiovascular development and disease.

A gene expression resource generated by genome-wide lacZ profiling in the mouse

N. Karp, R. Ramirez-Solis, D. Smedley, 2015, Disease Models & Mechanisms.

Common and distinct transcriptional signatures of mammalian embryonic lethality

Jacqueline K. White, D. Adams, I. Sealy, 2019, Nature Communications.

High-throughput discovery of novel developmental phenotypes

Lisa X. Yu, Jacqueline K. White, Juan J. Gallegos, 2016, Nature.

Genetic determinants of micronucleus formation in vivo

A. Speak, R. McIntyre, W. Skarnes, 2024, Nature.