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Humanin P3S, haplogroup N1b and the risk of Alzheimer's disease

Aging cell, 2024-07, Vol.23 (7), p.e14207-n/a

Logan, Ian Stewart

2024

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Pseudogenization of the Humanin gene is common in the mitochondrial DNA of many vertebrates

Dōngwùxué yánjiū, 2017-07, Vol.38 (4), p.198

Logan, Ian S

2017

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ZIKA--How fast does this virus mutate?

Dōngwùxué yánjiū, 2016-03, Vol.37 (2), p.110-115

Logan, Ian S

2016

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mtDNA Data Mining in GenBank Needs Surveying

American journal of human genetics, 2009-12, Vol.85 (6), p.929-933

2009

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Leber Hereditary Optic Neuropathy: A Mitochondrial Disease Unique in Many Ways

Handbook of experimental pharmacology, 2017, Vol.240, p.309-336

2017

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Recurrent somatic mutation of FAT1 in multiple human cancers leads to aberrant Wnt activation

Nature genetics, 2013-03, Vol.45 (3), p.253-261

2013

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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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Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencing

PloS one, 2014-08, Vol.9 (8), p.e104281-e104281

2014

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Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome

American journal of human genetics, 2008-08, Vol.83 (2), p.170-179

2008

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Restoring the natural tropism of AAV2 vectors for human liver

Science translational medicine, 2020-09, Vol.12 (560)

2020

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SARS-CoV-2 omicron BA.2.87.1 exhibits higher susceptibility to serum neutralization than EG.5.1 and JN.1

Emerging microbes & infections, 2024-12, Vol.13 (1), p.2359004

2024

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Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

American journal of human genetics, 2012-09, Vol.91 (3), p.565-571

2012

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An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Nature cell biology, 2015-08, Vol.17 (8), p.1074-1087

2015

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Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma

American journal of human genetics, 2011-09, Vol.89 (3), p.464-473

2011

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An Improved Small-Molecule Inhibitor of FtsZ with Superior In Vitro Potency, Drug-Like Properties, and In Vivo Efficacy

Antimicrobial Agents and Chemotherapy, 2013-01, Vol.57 (1), p.317-325

2013

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HACE1 deficiency causes an autosomal recessive neurodevelopmental syndrome

Journal of medical genetics, 2015-12, Vol.52 (12), p.797-803

2015

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Functional characterization of dehydratase/aminotransferase pairs from Helicobacter and Campylobacter: enzymes distinguishing the pseudaminic acid and bacillosamine biosynthetic pathways

The Journal of biological chemistry, 2006-01, Vol.281 (2), p.723-732

2006

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Structural and Functional Characterization of PseC, an Aminotransferase Involved in the Biosynthesis of Pseudaminic Acid, an Essential Flagellar Modification in Helicobacter pylori

The Journal of biological chemistry, 2006-03, Vol.281 (13), p.8907-8916

2006

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Identification of Novel Glycosyltransferases Required for Assembly of the Pasteurella multocida A:1 Lipopolysaccharide and Their Involvement in Virulence

Infection and Immunity, 2009-04, Vol.77 (4), p.1532-1542

2009

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Protein Glycosylation in Campylobacter jejuni: Partial Suppression of pglF by Mutation of pseC

Journal of Bacteriology, 2007-09, Vol.189 (18), p.6731-6733

2007

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Illuminator, a desktop program for mutation detection using short-read clonal sequencing

Genomics (San Diego, Calif.), 2011-10, Vol.98 (4), p.302-309

2011

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Humanin P3S, haplogroup N1b and the risk of Alzheimer's disease

Pseudogenization of the Humanin gene is common in the mitochondrial DNA of many vertebrates

ZIKA--How fast does this virus mutate?

mtDNA Data Mining in GenBank Needs Surveying

Leber Hereditary Optic Neuropathy: A Mitochondrial Disease Unique in Many Ways

Recurrent somatic mutation of FAT1 in multiple human cancers leads to aberrant Wnt activation

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

Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencing

CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium

Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)

Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome

The mutational landscape of adenoid cystic carcinoma

Restoring the natural tropism of AAV2 vectors for human liver

SARS-CoV-2 omicron BA.2.87.1 exhibits higher susceptibility to serum neutralization than EG.5.1 and JN.1

Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma

An Improved Small-Molecule Inhibitor of FtsZ with Superior In Vitro Potency, Drug-Like Properties, and In Vivo Efficacy

HACE1 deficiency causes an autosomal recessive neurodevelopmental syndrome

Functional characterization of dehydratase/aminotransferase pairs from Helicobacter and Campylobacter: enzymes distinguishing the pseudaminic acid and bacillosamine biosynthetic pathways

Structural and Functional Characterization of PseC, an Aminotransferase Involved in the Biosynthesis of Pseudaminic Acid, an Essential Flagellar Modification in Helicobacter pylori

Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

Identification of Novel Glycosyltransferases Required for Assembly of the Pasteurella multocida A:1 Lipopolysaccharide and Their Involvement in Virulence

Protein Glycosylation in Campylobacter jejuni: Partial Suppression of pglF by Mutation of pseC

Illuminator, a desktop program for mutation detection using short-read clonal sequencing

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