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An Archaeal Immune System Can Detect Multiple Protospacer Adjacent Motifs (PAMs) to Target Invader DNA

The Journal of biological chemistry, 2012-09, Vol.287 (40), p.33351-33363

2012

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A Complex of Cas Proteins 5, 6, and 7 Is Required for the Biogenesis and Stability of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-derived RNAs (crRNAs) in Haloferax volcanii

The Journal of biological chemistry, 2014-03, Vol.289 (10), p.7164-7177

2014

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The nuts and bolts of the Haloferax CRISPR-Cas system I-B

RNA biology, 2019-04, Vol.16 (4), p.469-480

2019

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The ring of confidence: a haloarchaeal CRISPR/Cas system

Biochemical Society transactions, 2013-02, Vol.41 (1), p.374-378

2013

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Requirements for a successful defence reaction by the CRISPR-Cas subtype I-B system

Biochemical Society transactions, 2013-12, Vol.41 (6), p.1444-1448

2013

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Small RNAs for defence and regulation in archaea

Extremophiles : life under extreme conditions, 2012-09, Vol.16 (5), p.685-696

2012

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The immune system of halophilic archaea

Mobile genetic elements, 2012-09, Vol.2 (5), p.228-232

2012

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The immune system of halophilic archaea

Mobile genetic elements, 2012-09, Vol.2 (5), p.0-1

2012

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Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model

Journal of molecular medicine (Berlin, Germany), 2011-04, Vol.89 (4), p.389-398

2011

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International Trial of the Edmonton Protocol for Islet Transplantation

The New England journal of medicine, 2006-09, Vol.355 (13), p.1318-1330

2006

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Molecular and biochemical characterization of a unique mutation in CCS, the human copper chaperone to superoxide dismutase

Human mutation, 2012-08, Vol.33 (8), p.1207-1215

2012

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Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin

American journal of human genetics, 2012-01, Vol.90 (1), p.61-68

2012

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Suppression of Nonsense Mutations in Rett Syndrome by Aminoglycoside Antibiotics

Pediatric research, 2009-05, Vol.65 (5), p.520-523

2009

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Characterization of the MeCP2R168X knockin mouse model for Rett syndrome

PloS one, 2014-12, Vol.9 (12), p.e115444-e115444

2014

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Characterization of the MeCP2.sup.R168X Knockin Mouse Model for Rett Syndrome

PloS one, 2014-12, Vol.9 (12)

2014

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Erratum to: Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model

Journal of molecular medicine (Berlin, Germany), 2013-06, Vol.91 (6), p.775-775

2013

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Methotrexate treatment of FraX fibroblasts results in FMR1 transcription but not in detectable FMR1 protein levels

Journal of neurodevelopmental disorders, 2013-09, Vol.5 (1), p.23-23, Article 23

2013

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Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2

American journal of medical genetics. Part A, 2005-08, Vol.137A (2), p.136-138

2005

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Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin

American journal of human genetics, 2012-02, Vol.90 (2), p.378-378

2012

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Expression of Interferon Regulatory Factor 4 in Chronic Myeloid Leukemia: Correlation With Response to Interferon Alfa Therapy

Journal of clinical oncology, 2000-10, Vol.18 (19), p.3331-3338

2000

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Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2−/y knockout mice

The Journal of physiology, 2007-03, Vol.579 (3), p.863-876

2007

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Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2â/y knockout mice

The Journal of physiology, 2007-03, Vol.579 (3), p.863

2007

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Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2

American journal of medical genetics, 2005, Vol.137A (2), p.136-138

2005

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An Archaeal Immune System Can Detect Multiple Protospacer Adjacent Motifs (PAMs) to Target Invader DNA

A Complex of Cas Proteins 5, 6, and 7 Is Required for the Biogenesis and Stability of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-derived RNAs (crRNAs) in Haloferax volcanii

The nuts and bolts of the Haloferax CRISPR-Cas system I-B

The ring of confidence: a haloarchaeal CRISPR/Cas system

Requirements for a successful defence reaction by the CRISPR-Cas subtype I-B system

Small RNAs for defence and regulation in archaea

The immune system of halophilic archaea

The immune system of halophilic archaea

Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model

International Trial of the Edmonton Protocol for Islet Transplantation

Molecular and biochemical characterization of a unique mutation in CCS, the human copper chaperone to superoxide dismutase

Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin

Suppression of Nonsense Mutations in Rett Syndrome by Aminoglycoside Antibiotics

Characterization of the MeCP2R168X knockin mouse model for Rett syndrome

Characterization of the MeCP2.sup.R168X Knockin Mouse Model for Rett Syndrome

Erratum to: Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model

Methotrexate treatment of FraX fibroblasts results in FMR1 transcription but not in detectable FMR1 protein levels

Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2

Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin

Expression of Interferon Regulatory Factor 4 in Chronic Myeloid Leukemia: Correlation With Response to Interferon Alfa Therapy

Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2−/y knockout mice

Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2â/y knockout mice

Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2

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