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Uptake, translocation, weathering and speciation of gold nanoparticles in potato, radish, carrot and lettuce crops

Journal of hazardous materials, 2021-09, Vol.418, p.126219, Article 126219

2021

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The pathogenic basis of malaria

Nature (London), 2002-02, Vol.415 (6872), p.673-679

2002

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Genetic diversity and chloroquine selective sweeps in Plasmodium falciparum

Nature (London), 2002-07, Vol.418 (6895), p.320-323

2002

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Implementing context information management in forensic casework: Minimizing contextual bias in firearms examination

Science & justice, 2016-03, Vol.56 (2), p.113-122

2016

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SFmap: a web server for motif analysis and prediction of splicing factor binding sites

Nucleic acids research, 2010-07, Vol.38 (Web Server issue), p.W281-W285

2010

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Pluripotent genes role in normal melanocyte lineage commitment and malignant transformation

European journal of cancer (1990), 2016-07, Vol.61, p.S109-S109

2016

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The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families

PloS one, 2015-08, Vol.10 (8), p.e0129631-e0129631

2015

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Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome

PloS one, 2020-08, Vol.15 (8), p.e0237999-e0237999

2020

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Abnormal display of PfEMP-1 on erythrocytes carrying haemoglobin C may protect against malaria

Nature, 2005-06, Vol.435 (7045), p.1117-1121

2005

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Unravelling the pathogenic role and genotype-phenotype correlation of the USH2A p.(Cys759Phe) variant among Spanish families

PloS one, 2018-06, Vol.13 (6), p.e0199048

2018

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De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa

PloS one, 2016-03, Vol.11 (3), p.e0150944-e0150944

2016

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Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families

PloS one, 2015-07, Vol.10 (7), p.e0131679-e0131679

2015

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Investigating the Molecular Basis of Retinal Degeneration in a Familial Cohort of Pakistani Decent by Exome Sequencing

PloS one, 2015-09, Vol.10 (9), p.e0136561-e0136561

2015

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Blue cone monochromacy: visual function and efficacy outcome measures for clinical trials

PloS one, 2015-04, Vol.10 (4), p.e0125700-e0125700

2015

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Dominant Retinitis Pigmentosa, p.Gly56Arg Mutation in NR2E3: Phenotype in a Large Cohort of 24 Cases

PloS one, 2016-02, Vol.11 (2), p.e0149473-e0149473

2016

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Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees

PloS one, 2015-09, Vol.10 (9), p.e0138072-e0138072

2015

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Predation Risk Perception, Food Density and Conspecific Cues Shape Foraging Decisions in a Tropical Lizard

PloS one, 2015-09, Vol.10 (9), p.e0138016-e0138016

2015

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A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population

PloS one, 2017-05, Vol.12 (5), p.e0177196-e0177196

2017

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Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations

PloS one, 2016-07, Vol.11 (7), p.e0158692-e0158692

2016

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Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons Learned

PloS one, 2015-07, Vol.10 (7), p.e0133624

2015

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Establishment of a Flexible Real-Time Polymerase Chain Reaction-Based Platform for Detecting Prevalent Deafness Mutations Associated with Variable Degree of Sensorineural Hearing Loss in Koreans

PloS one, 2016-09, Vol.11 (9), p.e0161756-e0161756

2016

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Cloning the P. falciparum gene encoding PfEMP1, a malarial variant antigen and adherence receptor on the surface of parasitized human erythrocytes

Cell, 1995-07, Vol.82 (1), p.77-87

1995

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Classification of adhesive domains in the Plasmodium falciparum Erythrocyte Membrane Protein 1 family

Molecular and biochemical parasitology, 2000-10, Vol.110 (2), p.293-310

2000

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Dependable and Efficient Clinical Molecular Diagnosis of Chinese RP Patient with Targeted Exon Sequencing

PloS one, 2015-10, Vol.10 (10), p.e0140684-e0140684

2015

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Mental Imagery and Aging

Psychology and aging, 1994-03, Vol.9 (1), p.90-102

1994

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Uptake, translocation, weathering and speciation of gold nanoparticles in potato, radish, carrot and lettuce crops

The pathogenic basis of malaria

Genetic diversity and chloroquine selective sweeps in Plasmodium falciparum

Implementing context information management in forensic casework: Minimizing contextual bias in firearms examination

SFmap: a web server for motif analysis and prediction of splicing factor binding sites

Pluripotent genes role in normal melanocyte lineage commitment and malignant transformation

The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families

Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome

Abnormal display of PfEMP-1 on erythrocytes carrying haemoglobin C may protect against malaria

Unravelling the pathogenic role and genotype-phenotype correlation of the USH2A p.(Cys759Phe) variant among Spanish families

De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa

Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families

Investigating the Molecular Basis of Retinal Degeneration in a Familial Cohort of Pakistani Decent by Exome Sequencing

Blue cone monochromacy: visual function and efficacy outcome measures for clinical trials

Dominant Retinitis Pigmentosa, p.Gly56Arg Mutation in NR2E3: Phenotype in a Large Cohort of 24 Cases

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees

Predation Risk Perception, Food Density and Conspecific Cues Shape Foraging Decisions in a Tropical Lizard

A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population

Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations

Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons Learned

Establishment of a Flexible Real-Time Polymerase Chain Reaction-Based Platform for Detecting Prevalent Deafness Mutations Associated with Variable Degree of Sensorineural Hearing Loss in Koreans

Cloning the P. falciparum gene encoding PfEMP1, a malarial variant antigen and adherence receptor on the surface of parasitized human erythrocytes

Classification of adhesive domains in the Plasmodium falciparum Erythrocyte Membrane Protein 1 family

Dependable and Efficient Clinical Molecular Diagnosis of Chinese RP Patient with Targeted Exon Sequencing

Mental Imagery and Aging

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