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Adverse childhood experiences, epigenetics and telomere length variation in childhood and beyond: a systematic review of the literature

European child & adolescent psychiatry, 2020-10, Vol.29 (10), p.1329-1338

2020

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A survey of the use of seclusion and physical restraint at school and at home for children under the care of the NHS Lanarkshire CAMHS – learning disability team

BJPsych open, 2021-06, Vol.7 (S1), p.S222-S222

2021

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Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome

Mammalian genome, 2000-08, Vol.11 (8), p.675-681

2000

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Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene

Genome research, 1998-08, Vol.8 (8), p.834

1998

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Mutations of UFD1L Are Not Responsible for the Majority of Cases of DiGeorge Syndrome/Velocardiofacial Syndrome without Deletions within Chromosome 22q11

American journal of human genetics, 1999-07, Vol.65 (1), p.247-249

1999

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A human gene similar to Drosophila melanogaster peanut maps to the DiGeorge syndrome region of 22q11

Human genetics, 1997-11, Vol.101 (1), p.6-12

1997

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Cloning and mapping of murine Nfe2l1

Genomics (San Diego, Calif.), 1995-02, Vol.25 (3), p.716-719

1995

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Molecular Characterisation of Murine Nfe2l1

McKie, Judith Mary

1998

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ProQuest

Molecular characterisation of murine Nfe211

McKie, Judith Mary

1998

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ProQuest

512. Interim Results of a Prospective Cohort Study to Monitor the Emergence of Resistance in Immunocompromised Non-Hospitalized Patients With COVID-19 Who Were Treated with Sotrovimab in Great Britain: LUNAR Study

Open forum infectious diseases, 2023-11, Vol.10 (Supplement_2)

2023

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Long term effects of denufosol tetrasodium in patients with cystic fibrosis

Journal of cystic fibrosis, 2012-12, Vol.11 (6), p.539-549

2012

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A Novel Tissue Inhibitor of Metalloproteinases-3 Mutation Reveals a Common Molecular Phenotype in Sorsby's Fundus Dystrophy

The Journal of biological chemistry, 2000-09, Vol.275 (35), p.27027

2000

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Arabinanase A from Pseudomonas fluorescens subsp. cellulosa exhibits both an endo- and an exo- mode of action

Biochemical journal, 1997-04, Vol.323 ( Pt 2) (2), p.547-555

1997

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A novel tissue inhibitor of metalloproteinases-3 mutation reveals a common molecular phenotype in Sorsby's fundus dystrophy

The Journal of biological chemistry, 2000-09, Vol.275 (35), p.27027-27031

2000

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Predictors of micronutrient status in men and women over 75 years old living in the community

British journal of nutrition, 2002-11, Vol.88 (5), p.555-561

2002

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Clinical features of a novel TIMP-3 mutation causing Sorsby's fundus dystrophy: implications for disease mechanism

British journal of ophthalmology, 2001-12, Vol.85 (12), p.1429-1431

2001

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Health and Education Working Together: The New South Wales School-Link Initiative

The international journal of mental health promotion, 2002-11, Vol.4 (4), p.36-43

2002

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Achieving positive health in older age: Developing a nutritional anthropology

Journal of the Institute of Health Education, 1994-01, Vol.32 (3), p.89-91

1994

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Adverse childhood experiences, epigenetics and telomere length variation in childhood and beyond: a systematic review of the literature

A survey of the use of seclusion and physical restraint at school and at home for children under the care of the NHS Lanarkshire CAMHS – learning disability team

Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome

Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene

Mutations of UFD1L Are Not Responsible for the Majority of Cases of DiGeorge Syndrome/Velocardiofacial Syndrome without Deletions within Chromosome 22q11

A human gene similar to Drosophila melanogaster peanut maps to the DiGeorge syndrome region of 22q11

Cloning and mapping of murine Nfe2l1

Molecular Characterisation of Murine Nfe2l1

Molecular characterisation of murine Nfe211

512. Interim Results of a Prospective Cohort Study to Monitor the Emergence of Resistance in Immunocompromised Non-Hospitalized Patients With COVID-19 Who Were Treated with Sotrovimab in Great Britain: LUNAR Study

Long term effects of denufosol tetrasodium in patients with cystic fibrosis

A Novel Tissue Inhibitor of Metalloproteinases-3 Mutation Reveals a Common Molecular Phenotype in Sorsby's Fundus Dystrophy

Arabinanase A from Pseudomonas fluorescens subsp. cellulosa exhibits both an endo- and an exo- mode of action

A novel tissue inhibitor of metalloproteinases-3 mutation reveals a common molecular phenotype in Sorsby's fundus dystrophy

Predictors of micronutrient status in men and women over 75 years old living in the community

Clinical features of a novel TIMP-3 mutation causing Sorsby's fundus dystrophy: implications for disease mechanism

Health and Education Working Together: The New South Wales School-Link Initiative

Achieving positive health in older age: Developing a nutritional anthropology

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