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Overexpression of miR-7977 in CD4+ T cells is associated with multiplex autoimmunity in patients with Addison's disease

European journal of endocrinology, 2021-07, Vol.185 (1), p.145-154

2021

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Genomic variants and inferred biological processes in multiplex families with Tourette syndrome

Journal of psychiatry & neuroscience, 2023-05, Vol.48 (3), p.E179-E189

2023

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Structural Variants and Implicated Processes Associated with Familial Tourette Syndrome

International journal of molecular sciences, 2024-06, Vol.25 (11), p.5758

2024

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Rapid increase in the incidence of type 1 diabetes in Polish children from 1989 to 2004, and predictions for 2010 to 2025

Diabetologia, 2011-03, Vol.54 (3), p.508-515

2011

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Can polygenic risk scores help explain disease prevalence differences around the world? A worldwide investigation

BMC genomic data, 2023-11, Vol.24 (1), p.70-70, Article 70

2023

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Rare Variant in the SLC6A2 Encoding a Norepinephrine Transporter Is Associated with Elite Athletic Performance in the Polish Population

Genes, 2021-06, Vol.12 (6), p.919

2021

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Pathogenic Mutations and Putative Phenotype-Affecting Variants in Polish Myofibrillar Myopathy Patients

Journal of clinical medicine, 2021-02, Vol.10 (5), p.914

2021

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Delayed recognition of Wolfram syndrome frequently misdiagnosed as type 1 diabetes with early chronic complications

Experimental and clinical endocrinology & diabetes, 2014-01, Vol.122 (1), p.35-38

2014

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PTPN22, PDCD1 and CYP27B1 polymorphisms and susceptibility to type 1 diabetes in Polish patients

International journal of immunogenetics, 2010-10, Vol.37 (5), p.367-372

2010

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Increased serum osteoprotegerin in patients with primary adrenal insufficiency receiving conventional hydrocortisone substitution

Journal of physiology and pharmacology : an official journal of the Polish Physiological Society, 2012-12, Vol.63 (6), p.677

2012

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Association of the CYP27B1 C(-1260)A polymorphism with autoimmune Addison's disease

Experimental and clinical endocrinology & diabetes, 2010-08, Vol.118 (8), p.544-549

2010

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Common polymorphism (81Val>Ile) and rare mutations (257Arg>Ser and 335Ile>Ser) of the MC3R gene in obese Polish children and adolescents

Molecular biology reports, 2013-12, Vol.40 (12), p.6893-6898

2013

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ANO5 mutations in the Polish limb girdle muscular dystrophy patients: Effects on the protein structure

Scientific reports, 2019-08, Vol.9 (1), p.11533-17, Article 11533

2019

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Effect of three common SNPs in 5′-flanking region of LEP and ADIPOQ genes on their expression in Polish obese children and adolescents

Molecular biology reports, 2012-04, Vol.39 (4), p.3951-3955

2012

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A novel dominant D109A CRYAB mutation in a family with myofibrillar myopathy affects αB-crystallin structure

BBA clinical, 2017-06, Vol.7, p.1-7

2017

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287 Cyp27B1 and Pdcd1 Polymorphisms in Polish Children with Type 1 Diabetes

Pediatric research, 2010-11, Vol.68, p.148-148

2010

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Overactive BRCA1 Affects Presenilin 1 in Induced Pluripotent Stem Cell-Derived Neurons in Alzheimer’s Disease

Journal of Alzheimer's disease, 2018-01, Vol.62 (1), p.175-202

2018

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Polymorphic variants of the IL2RA gene and susceptibility to type 1 diabetes in the Polish population

Tissue antigens, 2012-03, Vol.79 (3), p.198-203

2012

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P2 Individual indications for humalog therapy in diabetic children and adolescents cases

Diabetes research and clinical practice, 1999-04, Vol.44, p.S10-S10

Fichna, P.

1999

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Autoantibodies to IA-2 in insulin-dependent diabetes mellitus: Measurements with a new immunoprecipitation assay

Clinica chimica acta, 2000-01, Vol.291 (1), p.53-66

2000

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Sexual dimorphism in the expression of GAD65 autoantibodies at onset of type 1 diabetes in contrasting populations

Diabetes research and clinical practice, 2000-09, Vol.50, p.201-201

2000

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Cytochemical and functional evaluation of ACTH responsive isolated rat adrenocortical cells. The maintenance of sex differences

Folia histochemica et cytobiologica, 1987, Vol.25 (1), p.3

1987

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Association of chosen microsatellite markers on chromosomes 10, 11p and 14q with IDDM susceptibility in the population of midwestern Poland

Journal of applied genetics, 1996-01, Vol.37 (2), p.217-228

1996

Volltextzugriff (PDF)

In vitro studies of nuclear volume of rat adrenocortical cells: lace of ACTH effect

Zeitschrift fur mikroskopisch-anatomische Forschung, 1980, Vol.94 (4), p.721

1980

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Deletion mapping of interval 6 of the human Y chromosome

Human genetics, 1991-06, Vol.87 (2), p.234-236

1991

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Overexpression of miR-7977 in CD4+ T cells is associated with multiplex autoimmunity in patients with Addison's disease

Genomic variants and inferred biological processes in multiplex families with Tourette syndrome

Structural Variants and Implicated Processes Associated with Familial Tourette Syndrome

Rapid increase in the incidence of type 1 diabetes in Polish children from 1989 to 2004, and predictions for 2010 to 2025

Can polygenic risk scores help explain disease prevalence differences around the world? A worldwide investigation

Rare Variant in the SLC6A2 Encoding a Norepinephrine Transporter Is Associated with Elite Athletic Performance in the Polish Population

Pathogenic Mutations and Putative Phenotype-Affecting Variants in Polish Myofibrillar Myopathy Patients

Delayed recognition of Wolfram syndrome frequently misdiagnosed as type 1 diabetes with early chronic complications

PTPN22, PDCD1 and CYP27B1 polymorphisms and susceptibility to type 1 diabetes in Polish patients

Increased serum osteoprotegerin in patients with primary adrenal insufficiency receiving conventional hydrocortisone substitution

Association of the CYP27B1 C(-1260)A polymorphism with autoimmune Addison's disease

Common polymorphism (81Val>Ile) and rare mutations (257Arg>Ser and 335Ile>Ser) of the MC3R gene in obese Polish children and adolescents

ANO5 mutations in the Polish limb girdle muscular dystrophy patients: Effects on the protein structure

Effect of three common SNPs in 5′-flanking region of LEP and ADIPOQ genes on their expression in Polish obese children and adolescents

A novel dominant D109A CRYAB mutation in a family with myofibrillar myopathy affects αB-crystallin structure

287 Cyp27B1 and Pdcd1 Polymorphisms in Polish Children with Type 1 Diabetes

Overactive BRCA1 Affects Presenilin 1 in Induced Pluripotent Stem Cell-Derived Neurons in Alzheimer’s Disease

Polymorphic variants of the IL2RA gene and susceptibility to type 1 diabetes in the Polish population

P2 Individual indications for humalog therapy in diabetic children and adolescents cases

Autoantibodies to IA-2 in insulin-dependent diabetes mellitus: Measurements with a new immunoprecipitation assay

Sexual dimorphism in the expression of GAD65 autoantibodies at onset of type 1 diabetes in contrasting populations

Cytochemical and functional evaluation of ACTH responsive isolated rat adrenocortical cells. The maintenance of sex differences

Association of chosen microsatellite markers on chromosomes 10, 11p and 14q with IDDM susceptibility in the population of midwestern Poland

In vitro studies of nuclear volume of rat adrenocortical cells: lace of ACTH effect

Deletion mapping of interval 6 of the human Y chromosome

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