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Multilingual Global Cities: Singapore, Hong Kong, Dubai

1st, 2021

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Multi-modal access method (eye-tracking + switch-scanning) for individuals with severe motor impairment: A preliminary investigation

Assistive technology, 2023-07, Vol.35 (4), p.321-329

2023

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An epigenetic and transcriptomic signature of immune tolerance in human monocytes through multi-omics integration

Genome medicine, 2021-08, Vol.13 (1), p.131-131, Article 131

2021

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LAD-1/variant syndrome is caused by mutations in FERMT3

Blood, 2009-05, Vol.113 (19), p.4740-4746

2009

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SGCE isoform characterization and expression in human brain: implications for myoclonus―dystonia pathogenesis?

European journal of human genetics : EJHG, 2011-04, Vol.19 (4), p.438-444

2011

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Molecular pathology, developmental changes and synaptic dysfunction in (pre-) symptomatic human C9ORF72-ALS/FTD cerebral organoids

Acta neuropathologica communications, 2024-09, Vol.12 (1), p.152-31, Article 152

2024

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Amplified fragment length polymorphism and whole genome sequencing: a comparison of methods in the investigation of a nosocomial outbreak with vancomycin resistant enterococci

Antimicrobial resistance & infection control, 2019-09, Vol.8 (1), p.153-153, Article 153

2019

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In vivo tumor growth inhibition and biodistribution studies of locked nucleic acid (LNA) antisense oligonucleotides

Nucleic acids research, 2003-02, Vol.31 (3), p.953-962

2003

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Intracellular pyruvate levels positively correlate with cytokine production capacity in tolerant monocytes from patients with pneumonia

Biochimica et biophysica acta. Molecular basis of disease, 2022-11, Vol.1868 (11), p.166519-166519, Article 166519

2022

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SMARCB1/INI1 maternal germ line mosaicism in schwannomatosis

Clinical genetics, 2010-01, Vol.77 (1), p.86-91

2010

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Dynamic clonal hematopoiesis and functional T-cell immunity in a supercentenarian

Leukemia, 2021-07, Vol.35 (7), p.2125-2129

2021

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Indexing Authenticity: Sociolinguistic Perspectives

1st edition., 2014

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FIBROSCLEROSIS AND SCLEROSING ADENOSIS WITH MICROCALCIFICATIONS IN THE BREAST. MOLECULAR PATHOGENESIS, TIMELY DIAGNOSIS AND TREATMENT

Issledovaniâ i praktika v medicine, 2019-06, Vol.6 (2), p.75-85

2019

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A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy

Human molecular genetics, 2012-01, Vol.21 (2), p.358-370

2012

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Metagenomic DNA sequencing for semi-quantitative pathogen detection from urine: a prospective, laboratory-based, proof-of-concept study

The Lancet. Microbe, 2022-08, Vol.3 (8), p.e588-e597

2022

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Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnostics

Journal of medical genetics, 2013-09, Vol.50 (9), p.614-626

2013

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Human T-cell memory consists mainly of unexpanded clones

Immunology letters, 2010-09, Vol.133 (1), p.42-48

2010

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Streptococcus pneumoniae Arginine Synthesis Genes Promote Growth and Virulence in Pneumococcal Meningitis

The Journal of infectious diseases, 2014-06, Vol.209 (11), p.1781-1791

2014

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Engineered self-organization of neural networks using carbon nanotube clusters

Physica A, 2005-05, Vol.350 (2), p.611-621

2005

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Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene

The Journal of clinical investigation, 1996-08, Vol.98 (4), p.1028-1033

1996

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Corneale intrastromale Presbyopiebehandlung (IntraCor) mit dem Femtec-Femtosekundenlaser

Klinische Monatsblätter für Augenheilkunde, 2009, Vol.226 (S 01)

2009

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1-Thiomethoxsalen and 1-Thiopsoralen: Synthesis, Photobiological Properties, and Site Specific Reaction of Thiopsoralens with DNA

Journal of medicinal chemistry, 1995-03, Vol.38 (6), p.869-874

1995

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Improving User Experience for Passenger Information Systems. Prototypes and Reference Objects

IEEE transactions on professional communication, 2013-06, Vol.60 (2), p.120

2013

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Looking ultra deep: Short identical sequences and transcriptional slippage

Genomics (San Diego, Calif.), 2011-08, Vol.98 (2), p.90-95

2011

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Prevention of preterm delivery with vaginal progesterone in women with preterm labour (4P): randomised double‐blind placebo‐controlled trial

BJOG : an international journal of obstetrics and gynaecology, 2015-01, Vol.122 (1), p.80-91

2015

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Multilingual Global Cities: Singapore, Hong Kong, Dubai

Multi-modal access method (eye-tracking + switch-scanning) for individuals with severe motor impairment: A preliminary investigation

An epigenetic and transcriptomic signature of immune tolerance in human monocytes through multi-omics integration

LAD-1/variant syndrome is caused by mutations in FERMT3

SGCE isoform characterization and expression in human brain: implications for myoclonus―dystonia pathogenesis?

Molecular pathology, developmental changes and synaptic dysfunction in (pre-) symptomatic human C9ORF72-ALS/FTD cerebral organoids

Amplified fragment length polymorphism and whole genome sequencing: a comparison of methods in the investigation of a nosocomial outbreak with vancomycin resistant enterococci

In vivo tumor growth inhibition and biodistribution studies of locked nucleic acid (LNA) antisense oligonucleotides

Intracellular pyruvate levels positively correlate with cytokine production capacity in tolerant monocytes from patients with pneumonia

SMARCB1/INI1 maternal germ line mosaicism in schwannomatosis

Dynamic clonal hematopoiesis and functional T-cell immunity in a supercentenarian

Indexing Authenticity: Sociolinguistic Perspectives

FIBROSCLEROSIS AND SCLEROSING ADENOSIS WITH MICROCALCIFICATIONS IN THE BREAST. MOLECULAR PATHOGENESIS, TIMELY DIAGNOSIS AND TREATMENT

A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy

Metagenomic DNA sequencing for semi-quantitative pathogen detection from urine: a prospective, laboratory-based, proof-of-concept study

Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnostics

Human T-cell memory consists mainly of unexpanded clones

Streptococcus pneumoniae Arginine Synthesis Genes Promote Growth and Virulence in Pneumococcal Meningitis

Engineered self-organization of neural networks using carbon nanotube clusters

Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene

Corneale intrastromale Presbyopiebehandlung (IntraCor) mit dem Femtec-Femtosekundenlaser

1-Thiomethoxsalen and 1-Thiopsoralen: Synthesis, Photobiological Properties, and Site Specific Reaction of Thiopsoralens with DNA

Improving User Experience for Passenger Information Systems. Prototypes and Reference Objects

Looking ultra deep: Short identical sequences and transcriptional slippage

Prevention of preterm delivery with vaginal progesterone in women with preterm labour (4P): randomised double‐blind placebo‐controlled trial

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