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Rhinovirus and the developing lung

Paediatric respiratory reviews, 2014-09, Vol.15 (3), p.268-274

2014

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Recommendations for locus-specific databases and their curation

Human mutation, 2008, Vol.29 (1), p.2-5

2008

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structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases

Human mutation, 2007-10, Vol.28 (10), p.931-932

2007

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MRSA infection in cystic fibrosis patients leads to a more rapid decline in lung function

Journal of cystic fibrosis, 2010, Vol.9, p.S33-S33

2010

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MRSA infection in cystic fibrosis patients leads to a more rapid decline in lung function

Paediatric respiratory reviews, 2010, Vol.11, p.S26-S26

2010

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The role of rhinovirus infections in young children with cystic fibrosis

Journal of clinical virology, 2020-08, Vol.129, p.104478-104478, Article 104478

2020

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P077 The role of PCR testing for Pseudomonas aeruginosa in the airways of children with cystic fibrosis

Journal of cystic fibrosis, 2020-06, Vol.19, p.S77-S77

2020

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The retinoblastoma tumor suppressor pathway modulates the invasiveness of ErbB2-positive breast cancer

Oncogene, 2014-07, Vol.33 (30), p.3980-3991

2014

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Enhancement of spin Seebeck effect in Fe3O4/Pt thin films with α-Fe nanodroplets

Applied physics letters, 2023-10, Vol.123 (17)

2023

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Anomalous Nernst effect in Co2MnSi thin films

Journal of physics. D, Applied physics, 2019-11, Vol.53 (3)

2019

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The role of different human rhinovirus species in acute respiratory illnesses in childhood

Cox, D.W

2014

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Spin Seebeck effect in polycrystalline yttrium iron garnet pellets prepared by the solid-state method

Europhysics letters, 2019-05, Vol.126 (3), p.37001

2019

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Cloning and mapping of murine superoxide dismutase copper chaperone (Ccsd) and mapping of the human ortholog

Cytogenetics and cell genetics, 2000, Vol.88 (1-2), p.35

2000

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Twenty-four novel mutations in Wilson disease patients of predominantly European ancestry

Human mutation, 2005-09, Vol.26 (3), p.280-280

2005

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Polymorphisms in canine ATP7B: Candidate modifier of copper toxicosis in the Bedlington terrier

The veterinary journal (1997), 2008-08, Vol.177 (2), p.293-296

2008

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Long range restriction mapping of 13q14. 2 focused on the Wilson disease region

Genomics (San Diego, Calif.), 1993-06, Vol.16:3

1993

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Tandem Repeats 3′ of the IGHA Genes in the Human Immunoglobulin Heavy Chain Gene Cluster

Genomics (San Diego, Calif.), 1996-07, Vol.35 (1), p.189-195

1996

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Complete Physical Map of the Human Immunoglobulin Heavy Chain Constant Region Gene Complex

Proceedings of the National Academy of Sciences - PNAS, 1989-07, Vol.86 (14), p.5567-5571

1989

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Physical and genetic mapping of the serpin gene cluster at 14q32. 1: Allelic association and a unique haplotype associated with [alpha][sub 1]-antitrypsin deficiency

American journal of human genetics, 1994-07, Vol.55:1

1994

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Haplotype studies in Wilson disease

American journal of human genetics, 1994, Vol.54 (1), p.71-78

1994

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Characterization and chromosomal localization of five canine ATOX1 pseudogenes

Cytogenetics and cell genetics, 2001, Vol.93 (1-2), p.105

2001

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Physical Linkage of a Human Immunoglobulin Heavy Chain Variable Region Gene Segment to Diversity and Joining Region Elements

Proceedings of the National Academy of Sciences - PNAS, 1988-11, Vol.85 (21), p.8196-8200

1988

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Bgl II polymorphism for the α 1 antitrjpsin-related gene on chromosome 14

Nucleic acids research, 1987, Vol.15 (11), p.4701-4701

1987

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Activation of prorenin by proteases from polymorphonuclear leukocytes

Canadian journal of physiology and pharmacology, 1980-04, Vol.58 (4), p.406

1980

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Immunoglobulin heavy chain variable region polymorphisms and multiple sclerosis susceptibility

Journal of neuroimmunology, 1993-04, Vol.44 (1), p.77-83

1993

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Rhinovirus and the developing lung

Recommendations for locus-specific databases and their curation

structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases

MRSA infection in cystic fibrosis patients leads to a more rapid decline in lung function

MRSA infection in cystic fibrosis patients leads to a more rapid decline in lung function

The role of rhinovirus infections in young children with cystic fibrosis

P077 The role of PCR testing for Pseudomonas aeruginosa in the airways of children with cystic fibrosis

The retinoblastoma tumor suppressor pathway modulates the invasiveness of ErbB2-positive breast cancer

Enhancement of spin Seebeck effect in Fe3O4/Pt thin films with α-Fe nanodroplets

Anomalous Nernst effect in Co2MnSi thin films

The role of different human rhinovirus species in acute respiratory illnesses in childhood

Spin Seebeck effect in polycrystalline yttrium iron garnet pellets prepared by the solid-state method

Cloning and mapping of murine superoxide dismutase copper chaperone (Ccsd) and mapping of the human ortholog

Twenty-four novel mutations in Wilson disease patients of predominantly European ancestry

Polymorphisms in canine ATP7B: Candidate modifier of copper toxicosis in the Bedlington terrier

Long range restriction mapping of 13q14. 2 focused on the Wilson disease region

Tandem Repeats 3′ of the IGHA Genes in the Human Immunoglobulin Heavy Chain Gene Cluster

Complete Physical Map of the Human Immunoglobulin Heavy Chain Constant Region Gene Complex

Physical and genetic mapping of the serpin gene cluster at 14q32. 1: Allelic association and a unique haplotype associated with [alpha][sub 1]-antitrypsin deficiency

Haplotype studies in Wilson disease

Characterization and chromosomal localization of five canine ATOX1 pseudogenes

Physical Linkage of a Human Immunoglobulin Heavy Chain Variable Region Gene Segment to Diversity and Joining Region Elements

Bgl II polymorphism for the α 1 antitrjpsin-related gene on chromosome 14

Activation of prorenin by proteases from polymorphonuclear leukocytes

Immunoglobulin heavy chain variable region polymorphisms and multiple sclerosis susceptibility

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