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Antihyperglycemic effects of total flavonoids from Polygonatum odoratum in STZ and alloxan-induced diabetic rats

Journal of ethnopharmacology, 2009-07, Vol.124 (3), p.539-543

2009

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Rare cancer and return to work: experiences and needs of patients and (health care) professionals

Disability and rehabilitation, 2023-07, Vol.45 (16), p.2585-2596

2023

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The Analysis and Identification of P2P Botnet’s Traffic Flows

International journal of communication networks and information security, 2011-11, Vol.3 (2), p.138

2011

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Mutations in the CEP290 ( NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

American journal of human genetics, 2006-09, Vol.79 (3), p.556-561

2006

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Sucrose Induction of Anthocyanin Biosynthesis Mediated by DELLA

Molecular plant, 2014-03, Vol.7 (3), p.570-572

2014

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Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa

American journal of human genetics, 2008-11, Vol.83 (5), p.594-603

2008

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Application of low intensity ultrasound in the extraction of totally impacted mandibular third molars

Shanghai kou qiang yi xue, 2006-10, Vol.15 (5), p.497

2006

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Statistical Analysis on Characteristics of Gas Emission in a Fully Mechanized Caving Face under Drainage Conditions

Advanced materials research, 2013, Vol.734-737, p.634-637

2013

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Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 ( CRB1) Gene

American journal of human genetics, 2001-07, Vol.69 (1), p.198-203

2001

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CRB1 mutation spectrum in inherited retinal dystrophies

Human mutation, 2004-11, Vol.24 (5), p.355-369

2004

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Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Nature genetics, 1999-10, Vol.23 (2), p.217-221

1999

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Experimental Study on Thermal Performance of Steel Mesh Frame Sandwich Insulation Board

Applied Mechanics and Materials, 2012-08, Vol.193-194, p.847-851

2012

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Ocular and extra-ocular features of patients with Leber congenital amaurosis and mutations in CEP290

Molecular vision, 2012-02, Vol.18, p.412-425

2012

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Embedded Software Development with C

1, 2009

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A new Tone's method in APOLLO3® and its application to fast and thermal reactor calculations

Nuclear Engineering and Technology, 2017, 49(6), , pp.1269-1286

2017

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Bevacizumab in age‐related macular degeneration: a randomized controlled trial on the effect of injections every 4 weeks, 6 weeks and 8 weeks

Acta ophthalmologica (Oxford, England), 2013-09, Vol.91 (6), p.e456-e461

2013

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Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis

Investigative ophthalmology & visual science, 2006-03, Vol.47 (3), p.1167-1176

2006

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Evolution of microvoids in PAN-based carbon fibers

New Carbon Materials, 2010-02, Vol.25 (1), p.41-47

2010

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Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon

Human genetics, 2003-08, Vol.113 (3), p.268-275

2003

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Clinical relevance of straylight in patients with retinitis pigmentosa

Acta ophthalmologica (Oxford, England), 2012-09, Vol.90 (s249), p.0-0

2012

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Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa

European journal of human genetics : EJHG, 2004-12, Vol.12 (12), p.1024-1032

2004

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Homogeneous phenomenon of the graft when using different genotype characteristic of recipients/donors in living donor liver transplantation

World journal of hepatology, 2013-11, Vol.5 (11), p.642-648

2013

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A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

Journal of medical genetics, 2003-09, Vol.40 (9), p.709-713

2003

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OR11-002 - Mutations in MVK cause non-syndromic RP

Pediatric rheumatology online journal, 2013-11, Vol.11 (S1), p.A191-A191, Article A191

2013

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Antihyperglycemic effects of total flavonoids from Polygonatum odoratum in STZ and alloxan-induced diabetic rats

Rare cancer and return to work: experiences and needs of patients and (health care) professionals

The Analysis and Identification of P2P Botnet’s Traffic Flows

Mutations in the CEP290 ( NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides

Sucrose Induction of Anthocyanin Biosynthesis Mediated by DELLA

Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa

Application of low intensity ultrasound in the extraction of totally impacted mandibular third molars

Statistical Analysis on Characteristics of Gas Emission in a Fully Mechanized Caving Face under Drainage Conditions

Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 ( CRB1) Gene

CRB1 mutation spectrum in inherited retinal dystrophies

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Experimental Study on Thermal Performance of Steel Mesh Frame Sandwich Insulation Board

Ocular and extra-ocular features of patients with Leber congenital amaurosis and mutations in CEP290

Embedded Software Development with C

A new Tone's method in APOLLO3® and its application to fast and thermal reactor calculations

Bevacizumab in age‐related macular degeneration: a randomized controlled trial on the effect of injections every 4 weeks, 6 weeks and 8 weeks

Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis

Evolution of microvoids in PAN-based carbon fibers

Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon

Clinical relevance of straylight in patients with retinitis pigmentosa

Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa

Homogeneous phenomenon of the graft when using different genotype characteristic of recipients/donors in living donor liver transplantation

A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

OR11-002 - Mutations in MVK cause non-syndromic RP

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