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The origin and evolution of cell types

Nature reviews. Genetics, 2016-12, Vol.17 (12), p.744

2016

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Induction of Antagonistic Soluble Decoy Receptor Tyrosine Kinases by Intronic PolyA Activation

Molecular cell, 2011-09, Vol.43 (6), p.927-939

2011

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A type III effector antagonizes death receptor signalling during bacterial gut infection

Nature (London), 2013-09, Vol.501 (7466), p.247-251

2013

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Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions

Nature genetics, 2019-01, Vol.51 (1), p.96-105

2019

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Neural crest origin of olfactory ensheathing glia

Proceedings of the National Academy of Sciences - PNAS, 2010-12, Vol.107 (49), p.21040-21045

2010

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Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte

American journal of human genetics, 2011-09, Vol.89 (3), p.451-458

2011

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The development of lateral line placodes: Taking a broader view

Developmental biology, 2014-05, Vol.389 (1), p.68-81

2014

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Mutations in TJP2 cause progressive cholestatic liver disease

Nature genetics, 2014-04, Vol.46 (4), p.326-328

2014

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Patrolling monocytes promote intravascular neutrophil activation and glomerular injury in the acutely inflamed glomerulus

Proceedings of the National Academy of Sciences - PNAS, 2016-08, Vol.113 (35), p.E5172-E5181

2016

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The evolution and development of vertebrate lateral line electroreceptors

Journal of experimental biology, 2013-07, Vol.216 (Pt 13), p.2515-2522

2013

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Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain

American journal of human genetics, 2015-12, Vol.97 (6), p.878-885

2015

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The molecular basis of how buried human leukocyte antigen polymorphism modulates natural killer cell function

Proceedings of the National Academy of Sciences - PNAS, 2020-05, Vol.117 (21), p.11636-11647

2020

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Evolution of the hypoxia-sensitive cells involved in amniote respiratory reflexes

eLife, 2017-04, Vol.6

2017

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Distinct Roles of the Antiapoptotic Effectors NleB and NleF from Enteropathogenic Escherichia coli

Infection and immunity, 2017-04, Vol.85 (4)

2017

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Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta

American journal of human genetics, 2016-10, Vol.99 (4), p.984-990

2016

Volltextzugriff (PDF)

Don’t eavesdrop!—Listen! Hearing an older person’s story in Atwood’s The Blind Assassin

European geriatric medicine, 2021-10, Vol.12 (5), p.1113-1114

Bostock, Clare V.

2021

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Identification of Mutations in SLC24A4, Encoding a Potassium-Dependent Sodium/Calcium Exchanger, as a Cause of Amelogenesis Imperfecta

American journal of human genetics, 2013-02, Vol.92 (2), p.307-312

2013

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CD4 + T cell calibration of antigen-presenting cells optimizes antiviral CD8 + T cell immunity

Nature immunology, 2023-06, Vol.24 (6), p.979

2023

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Splicing factor hnRNPH drives an oncogenic splicing switch in gliomas

The EMBO journal, 2011-10, Vol.30 (19), p.4084-4097

2011

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Feminisation: threat or opportunity?

Veterinary record, 2016-04, Vol.178 (16), p.391-393

Allen, L. Clare V.

2016

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Pathogenic Variants in PIGG Cause Intellectual Disability with Seizures and Hypotonia

American journal of human genetics, 2016-04, Vol.98 (4), p.615-626

2016

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Assisted reproductive technology in Australia and New Zealand: cumulative live birth rates as measures of success

Medical journal of Australia, 2017-08, Vol.207 (3), p.114-118

2017

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Specification of GnRH-1 neurons by antagonistic FGF and retinoic acid signaling

Developmental biology, 2012-02, Vol.362 (2), p.254-262

2012

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Insights into Electroreceptor Development and Evolution from Molecular Comparisons with Hair Cells

Integrative and comparative biology, 2018-08, Vol.58 (2), p.329-340

2018

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The origin and evolution of cell types

Induction of Antagonistic Soluble Decoy Receptor Tyrosine Kinases by Intronic PolyA Activation

A type III effector antagonizes death receptor signalling during bacterial gut infection

Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions

Neural crest origin of olfactory ensheathing glia

Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte

The development of lateral line placodes: Taking a broader view

Mutations in TJP2 cause progressive cholestatic liver disease

Patrolling monocytes promote intravascular neutrophil activation and glomerular injury in the acutely inflamed glomerulus

The evolution and development of vertebrate lateral line electroreceptors

Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain

The molecular basis of how buried human leukocyte antigen polymorphism modulates natural killer cell function

Evolution of the hypoxia-sensitive cells involved in amniote respiratory reflexes

Distinct Roles of the Antiapoptotic Effectors NleB and NleF from Enteropathogenic Escherichia coli

Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta

Don’t eavesdrop!—Listen! Hearing an older person’s story in Atwood’s The Blind Assassin

Identification of Mutations in SLC24A4, Encoding a Potassium-Dependent Sodium/Calcium Exchanger, as a Cause of Amelogenesis Imperfecta

CD4 + T cell calibration of antigen-presenting cells optimizes antiviral CD8 + T cell immunity

Splicing factor hnRNPH drives an oncogenic splicing switch in gliomas

Feminisation: threat or opportunity?

Pathogenic Variants in PIGG Cause Intellectual Disability with Seizures and Hypotonia

Assisted reproductive technology in Australia and New Zealand: cumulative live birth rates as measures of success

Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia

Specification of GnRH-1 neurons by antagonistic FGF and retinoic acid signaling

Insights into Electroreceptor Development and Evolution from Molecular Comparisons with Hair Cells

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