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Loss of Neutrophil Homing to the Periodontal Tissues Modulates the Composition and Disease Potential of the Oral Microbiota

Infection and immunity, 2021-11, Vol.89 (12), p.e0030921-e0030921

2021

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Horizontal and Vertical Transfer of Oral Microbial Dysbiosis and Periodontal Disease

Journal of dental research, 2019-12, Vol.98 (13), p.1503-1510

2019

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Current Practice in Forensic Medicine, Volume 3

1, 2022

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Mutations in the Retinal Guanylate Cyclase (RETGC-1) Gene in Dominant Cone-Rod Dystrophy

Human molecular genetics, 1998-07, Vol.7 (7), p.1179-1184

1998

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

Nature genetics, 2000-01, Vol.24 (1), p.79-83

2000

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Halothane genotype, pre-slaughter handling and stunning method all influence pork quality

Meat science, 2000-11, Vol.56 (3), p.291-299

2000

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Coccidia-induced mucogenesis promotes the onset of necrotic enteritis by supporting Clostridium perfringens growth

Veterinary immunology and immunopathology, 2008-03, Vol.122 (1), p.104-115

2008

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A Mutation in Guanylate Cyclase Activator 1A (GUCA1A) in an Autosomal Dominant Cone Dystrophy Pedigree Mapping to a New Locus on Chromosome 6p21.1

Human molecular genetics, 1998-02, Vol.7 (2), p.273-277

1998

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Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies

Journal of medical genetics, 2001-09, Vol.38 (9), p.611-614

2001

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Comparison of CO2 stunning with manual electrical stunning (50 Hz) of pigs on carcass and meat quality

Meat science, 2002, Vol.60 (1), p.63-68

2002

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The use of an e-learning constructivist solution in workplace learning

International journal of industrial ergonomics, 2009-05, Vol.39 (3), p.548-553

2009

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A Novel Locus for Leber Congenital Amaurosis (LCA4) with Anterior Keratoconus Mapping to Chromosome 17p13

Investigative ophthalmology & visual science, 2000-03, Vol.41 (3), p.629-633

2000

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Ligand-Specific Opening of a Gated-Porin Channel in the Outer Membrane of Living Bacteria

Science (American Association for the Advancement of Science), 1997-05, Vol.276 (5316), p.1261-1264

1997

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Current Practice in Forensic Medicine, Volume 2

John A. M. Gall, Jason Payne-James / John A. M. Gall, Jason Payne-James

2016

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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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Spectroscopic diagnostics of chemical processes: applications of tunable optical parametric oscillators

Applied physics. B, Lasers and optics, 2000-11, Vol.71 (5), p.651-663

2000

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Neurogenesis of excitation-contraction uncoupling in aging skeletal muscle

Exercise and sport sciences reviews, 2004-01, Vol.32 (1), p.36-40

2004

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Founder Effect, Seen in the British Population, of the 172 Peripherin/RDS Mutation—and Further Refinement of Genetic Positioning of the Peripherin/RDS Gene

American journal of human genetics, 1998-01, Vol.62 (1), p.192-195

1998

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A Locus for Autosomal Recessive Congenital Microphthalmia Maps to Chromosome 14q32

American journal of human genetics, 1998-05, Vol.62 (5), p.1113-1116

1998

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Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies

Journal of medical genetics, 1999-09, Vol.36 (9), p.691-693

1999

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The Routledge Handbook of Social Work Theory

1st edition., 2019

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Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32

British journal of ophthalmology, 1999-08, Vol.83 (8), p.919-922

1999

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A New Locus for Autosomal Recessive RP (RP29) Mapping to Chromosome 4q32-q34 in a Pakistani Family

Investigative ophthalmology & visual science, 2001-06, Vol.42 (7), p.1436-1438

2001

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A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

Nature genetics, 1999-04, Vol.21 (4), p.355-356

1999

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Corporal punishment in elementary education: Views of Barbadian schoolchildren

Child abuse & neglect, 1994-04, Vol.18 (4), p.377-386

1994

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Loss of Neutrophil Homing to the Periodontal Tissues Modulates the Composition and Disease Potential of the Oral Microbiota

Horizontal and Vertical Transfer of Oral Microbial Dysbiosis and Periodontal Disease

Current Practice in Forensic Medicine, Volume 3

Mutations in the Retinal Guanylate Cyclase (RETGC-1) Gene in Dominant Cone-Rod Dystrophy

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

Halothane genotype, pre-slaughter handling and stunning method all influence pork quality

Coccidia-induced mucogenesis promotes the onset of necrotic enteritis by supporting Clostridium perfringens growth

A Mutation in Guanylate Cyclase Activator 1A (GUCA1A) in an Autosomal Dominant Cone Dystrophy Pedigree Mapping to a New Locus on Chromosome 6p21.1

Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies

Comparison of CO2 stunning with manual electrical stunning (50 Hz) of pigs on carcass and meat quality

The use of an e-learning constructivist solution in workplace learning

A Novel Locus for Leber Congenital Amaurosis (LCA4) with Anterior Keratoconus Mapping to Chromosome 17p13

Ligand-Specific Opening of a Gated-Porin Channel in the Outer Membrane of Living Bacteria

Current Practice in Forensic Medicine, Volume 2

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

Spectroscopic diagnostics of chemical processes: applications of tunable optical parametric oscillators

Neurogenesis of excitation-contraction uncoupling in aging skeletal muscle

Founder Effect, Seen in the British Population, of the 172 Peripherin/RDS Mutation—and Further Refinement of Genetic Positioning of the Peripherin/RDS Gene

A Locus for Autosomal Recessive Congenital Microphthalmia Maps to Chromosome 14q32

Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies

The Routledge Handbook of Social Work Theory

Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32

A New Locus for Autosomal Recessive RP (RP29) Mapping to Chromosome 4q32-q34 in a Pakistani Family

A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

Corporal punishment in elementary education: Views of Barbadian schoolchildren

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