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EXPRESSION OF THE DEVELOPMENTAL AND ONCOGENIC PAX2 GENE IN HUMAN PROSTATE CANCER

The Journal of urology, 2001-06, Vol.165 (6), p.2115-2120

2001

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Molecular mapping of alzheimer-type dementia in Down's syndrome

Annals of neurology, 1998-03, Vol.43 (3), p.380-383

1998

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Juliusz Kessling

BMJ (Online), 2020-09, p.m3663

Kessling, Anna M

2020

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Association of the TNF-α-308 (G→A) polymorphism with self-reported history of childhood asthma

Human genetics, 2000-12, Vol.107 (6), p.591-596

2000

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MTHFR association with arteriosclerotic vascular disease?

Human genetics, 1998-07, Vol.103 (1), p.11-21

1998

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Allelic variability in D21S11, but not in APP or APOE, is associated with cognitive decline in Down syndrome

Neuroreport, 1997-05, Vol.8 (7), p.1645-1649

1997

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Influences of common variants of apolipoprotein E on measures of lipid metabolism in a sample selected for health

Arteriosclerosis and thrombosis, 1991-07, Vol.11 (4), p.1100-1110

1991

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Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?

Human genetics, 2000-11, Vol.107 (5), p.476-482

2000

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Sources of Variation in Plasma Lipid and Lipoprotein Traits in a Sample Selected for Health

American journal of epidemiology, 1999-12, Vol.150 (11), p.1229-1237

1999

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Etiology and pathogenesis of down syndrome

Early human development, 1996-09, Vol.46 (1-2), p.175-176

Kessling, Anna M.

1996

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Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction

Human genetics, 2000-05, Vol.106 (5), p.525-530

2000

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Novel Methodology for the Detection of Chromosome 21-Specific α-Satellite DNA Sequences

Genomics (San Diego, Calif.), 1999-05, Vol.57 (3), p.429-432

1999

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EXPRESSION OF THE DEVELOPMENTAL AND ONCOGENIC PAX2 GENE IN HUMAN PROSTATE CANCER

The Journal of urology, 2001-06, p.2115-2120

2001

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Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction

Human genetics, 2000-05, Vol.106 (5), p.525-530

2000

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Association of the TNF-[alpha]-308 (G[arrow right]A) polymorphism with self-reported history of childhood asthma

Human genetics, 2000-12, Vol.107 (6), p.591-596

2000

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THE DEVELOPMENTAL AND ONCOGENIC GENES PAX2, 5 & 8 ARE EXPRESSED IN TRANSITIONAL CELL CARCINOMA OF THE BLADDER

The Journal of urology, 1999-04, p.123

1999

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Apolipoprotein B gene variants are involved in the determination of serum cholesterol levels: a study in normo- and hypelipidaemic individuals

Atherosclerosis, 1987, Vol.67 (1), p.81-89

1987

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Identification of a second "French Canadian" LDL receptor gene deletion and development of a rapid method to detect both deletions

Clinical genetics, 1989-10, Vol.36 (4), p.219-228

1989

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Unusual genotypes in the COL6A1 gene in parents of children with trisomy 21 and major congenital heart defects

Human genetics, 1994-04, Vol.93 (4), p.443-446

1994

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Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect

American journal of human genetics, 1993-08, Vol.53 (2), p.462-471

1993

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The Problem of Polygenic Disease

Ciba Foundation Symposium 149 ‐ Human Genetic Information: Science, Law and Ethics, 2007, p.63-80

2007

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Variations in the apolipoprotein AI-CIII-AIV gene region and in lecithin: cholesterol acyltransferase concentration are determinants of plasma cholesterol concentrations

Atherosclerosis, 1988-03, Vol.70 (1), p.13-19

1988

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A PvuII polymorphism in the 5' flanking region of the apolipoprotein AIV gene: its use to study genetic variation determining serum lipid and apolipoprotein concentration

Human genetics, 1988-03, Vol.78 (3), p.237-239

1988

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A Phenocopy of Type III Dysbetalipoproteinemia Occurring in a Candidate Family for a Putative Apo E Receptor Defect

Annals of medicine (Helsinki), 1991, Vol.23 (2), p.161-167

1991

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Use of DNA Polymorphisms of the Apolipoprotein Genes to Study the Role of Genetic Variation in the Determination of Serum Lipid Levels

Ciba Foundation Symposium 130 ‐ Molecular Approaches to Human Polygenic Disease, 2007, p.128-149

2007

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EXPRESSION OF THE DEVELOPMENTAL AND ONCOGENIC PAX2 GENE IN HUMAN PROSTATE CANCER

Molecular mapping of alzheimer-type dementia in Down's syndrome

Juliusz Kessling

Association of the TNF-α-308 (G→A) polymorphism with self-reported history of childhood asthma

MTHFR association with arteriosclerotic vascular disease?

Allelic variability in D21S11, but not in APP or APOE, is associated with cognitive decline in Down syndrome

Influences of common variants of apolipoprotein E on measures of lipid metabolism in a sample selected for health

Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?

Sources of Variation in Plasma Lipid and Lipoprotein Traits in a Sample Selected for Health

Etiology and pathogenesis of down syndrome

Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction

Novel Methodology for the Detection of Chromosome 21-Specific α-Satellite DNA Sequences

EXPRESSION OF THE DEVELOPMENTAL AND ONCOGENIC PAX2 GENE IN HUMAN PROSTATE CANCER

Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction

Association of the TNF-[alpha]-308 (G[arrow right]A) polymorphism with self-reported history of childhood asthma

THE DEVELOPMENTAL AND ONCOGENIC GENES PAX2, 5 & 8 ARE EXPRESSED IN TRANSITIONAL CELL CARCINOMA OF THE BLADDER

Apolipoprotein B gene variants are involved in the determination of serum cholesterol levels: a study in normo- and hypelipidaemic individuals

Identification of a second "French Canadian" LDL receptor gene deletion and development of a rapid method to detect both deletions

Unusual genotypes in the COL6A1 gene in parents of children with trisomy 21 and major congenital heart defects

Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect

The Problem of Polygenic Disease

Variations in the apolipoprotein AI-CIII-AIV gene region and in lecithin: cholesterol acyltransferase concentration are determinants of plasma cholesterol concentrations

A PvuII polymorphism in the 5' flanking region of the apolipoprotein AIV gene: its use to study genetic variation determining serum lipid and apolipoprotein concentration

A Phenocopy of Type III Dysbetalipoproteinemia Occurring in a Candidate Family for a Putative Apo E Receptor Defect

Use of DNA Polymorphisms of the Apolipoprotein Genes to Study the Role of Genetic Variation in the Determination of Serum Lipid Levels

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