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Newborn screening for cystic fibrosis: Polish 4 years' experience with CFTR sequencing strategy

European journal of human genetics : EJHG, 2013-04, Vol.21 (4), p.391-396

2013

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Perspectives on tracking data reuse across biodata resources

Bioinformatics advances, 2024, Vol.4 (1), p.vbae057

2024

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Cycles of gene expression and genome response during mammalian tissue regeneration

Epigenetics & chromatin, 2018-09, Vol.11 (1), p.52-52, Article 52

2018

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1441PPROGRAMMED DEATH LIGAND-1 (PD-L1) EXPRESSION AND PROGNOSTIC VALUE IN SYNOVIAL SARCOMA

Annals of oncology, 2014-09, Vol.25 (suppl_4), p.iv503-iv504

2014

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Programmed Death Ligand-1 (Pd-L1) Expression and Prognostic Value in Synovial Sarcoma

Annals of oncology, 2014-09, Vol.25, p.iv503

2014

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MBDBMetrics: an online metrics tool to measure the impact of biological data resources

Bioinformatics advances, 2023, Vol.3 (1), p.vbad180-vbad180

2023

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Gene structure and chromosomal localization of the human P2X7 receptor

Receptors & channels, 1998, Vol.5 (6), p.347

1998

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Sodruzestvo Nezavisimych Gosudarstv v 2010 godu: Statisticeskiy ezegodnik

Mezgosudarstvennyj Statisticeskiy Komitet Sodruzestva Nezavisimych Gos

2011

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Schizophrenia and chromosomal deletions within 22q11.2

American journal of human genetics, 1995-06, Vol.56 (6), p.1502-1503

1995

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Fortuitous detection of uniparental isodisomy of chromosome 6

Journal of medical genetics, 1997-01, Vol.34 (1), p.77-78

1997

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Mapping of the Gene for the p60 Subunit of the Human Chromatin Assembly Factor (CAF1A) to the Down Syndrome Region of Chromosome 21

Genomics (San Diego, Calif.), 1996-04, Vol.33 (2), p.309-312

1996

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Localization of a Human Homolog of the Mouse Pericentrin Gene (PCNT) to Chromosome 21qter

Genomics (San Diego, Calif.), 1996-08, Vol.35 (3), p.620-624

1996

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Isolation and characterization of the mouse Aire gene

Biochemical and biophysical research communications, 1999-02, Vol.255 (2), p.483-490

1999

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Single-minded and Down syndrome?

Nature genetics, 1995-05, Vol.10 (1), p.9-10

1995

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O17 - The mTOR kinase directly regulates FBP1 gene expression via interaction with SWI/SNF chromatin remodeling complex in clear cell renal cell carcinoma (ccRCC)

European urology supplements : official journal of the European Association of Urology, 2019-10, Vol.18 (8), p.e3056-e3056

2019

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The mTOR kinase directly regulates FBP1 gene expression via interaction with SWI/SNF chromatin remodeling complex in clear cell renal cell carcinoma (ccRCC)

European urology supplements : official journal of the European Association of Urology, 2019-10, Vol.18 (8), p.e3056

2019

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A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y

Human genetics, 1999-11, Vol.105 (5), p.399-409

1999

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A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination

American journal of human genetics, 1995-08, Vol.57 (2), p.388-394

1995

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Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency

Human mutation, 1997, Vol.10 (6), p.430-435

1997

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Attention to adjacent and separate positions in space : an electrophysiological analysis

Perception & psychophysics, 1994-07, Vol.56 (1), p.42-52

1994

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Assignment 1 of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping

Cytogenetic and genome research, 1999-12, Vol.84 (3-4), p.188-189

1999

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Polarized secretion of urokinase-type plasminogen activator by epithelial cells

Experimental cell research, 1992-11, Vol.203 (1), p.236-243

1992

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Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping

Cytogenetics and cell genetics, 1999, Vol.84 (3-4), p.188

1999

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The Gene for Human U2 snRNP Auxiliary Factor Small 35-kDa Subunit (U2AF1) Maps to the Progressive Myoclonus Epilepsy (EPM1) Critical Region on Chromosome 21q22.3

Genomics (San Diego, Calif.), 1996-04, Vol.33 (2), p.298-300

1996

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NEUROPROTECTIVE EFFECTS OF SWIMMING TRAINING IN A MOUSE MODEL OF PARKINSON'S DISEASE INDUCED BY 6-HYDROXYDOPAMINE

Neuroscience, 2014, Vol.256, p.61-71

2014

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Newborn screening for cystic fibrosis: Polish 4 years' experience with CFTR sequencing strategy

Perspectives on tracking data reuse across biodata resources

Cycles of gene expression and genome response during mammalian tissue regeneration

1441PPROGRAMMED DEATH LIGAND-1 (PD-L1) EXPRESSION AND PROGNOSTIC VALUE IN SYNOVIAL SARCOMA

Programmed Death Ligand-1 (Pd-L1) Expression and Prognostic Value in Synovial Sarcoma

MBDBMetrics: an online metrics tool to measure the impact of biological data resources

Gene structure and chromosomal localization of the human P2X7 receptor

Sodruzestvo Nezavisimych Gosudarstv v 2010 godu: Statisticeskiy ezegodnik

Schizophrenia and chromosomal deletions within 22q11.2

Fortuitous detection of uniparental isodisomy of chromosome 6

Mapping of the Gene for the p60 Subunit of the Human Chromatin Assembly Factor (CAF1A) to the Down Syndrome Region of Chromosome 21

Localization of a Human Homolog of the Mouse Pericentrin Gene (PCNT) to Chromosome 21qter

Isolation and characterization of the mouse Aire gene

Single-minded and Down syndrome?

O17 - The mTOR kinase directly regulates FBP1 gene expression via interaction with SWI/SNF chromatin remodeling complex in clear cell renal cell carcinoma (ccRCC)

The mTOR kinase directly regulates FBP1 gene expression via interaction with SWI/SNF chromatin remodeling complex in clear cell renal cell carcinoma (ccRCC)

A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y

A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination

Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency

Attention to adjacent and separate positions in space : an electrophysiological analysis

Assignment 1 of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping

Polarized secretion of urokinase-type plasminogen activator by epithelial cells

Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping

The Gene for Human U2 snRNP Auxiliary Factor Small 35-kDa Subunit (U2AF1) Maps to the Progressive Myoclonus Epilepsy (EPM1) Critical Region on Chromosome 21q22.3

NEUROPROTECTIVE EFFECTS OF SWIMMING TRAINING IN A MOUSE MODEL OF PARKINSON'S DISEASE INDUCED BY 6-HYDROXYDOPAMINE

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