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NUP98 Dysregulation in Myeloid Leukemogenesis

Annals of the New York Academy of Sciences, 2007-06, Vol.1106 (1), p.114-142

2007

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Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome

Journal of medical genetics, 2004-08, Vol.41 (8), p.609-614

2004

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Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

Journal of medical genetics, 1999-04, Vol.36 (4), p.290-294

1999

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TRAIL (Apo2l) suppresses growth of primary human leukemia and myelodysplasia progenitors

Leukemia, 2002, Vol.16 (1), p.67-73

2002

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Shared and individual specificities of immunodominant cytotoxic T-cell clones in paroxysmal nocturnal hemoglobinuria as determined by molecular analysis

Experimental hematology, 2004-03, Vol.32 (3), p.261-269

2004

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In-vivo dominant immune responses in aplastic anaemia: molecular tracking of putatively pathogenetic T-cell clones by TCR β-CDR3 sequencing

The Lancet (British edition), 2004-07, Vol.364 (9431), p.355-364

2004

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Mitochondria Play a Central Role in Apoptosis Induced by α-Tocopheryl Succinate, an Agent with Antineoplastic Activity: Comparison with Receptor-Mediated Pro-Apoptotic Signaling

Biochemistry (Easton), 2003-04, Vol.42 (14), p.4277-4291

2003

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Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers

Cancer research (Chicago, Ill.), 2006-01, Vol.66 (2), p.659-664

2006

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Molecular Analysis of TCR Clonotypes in LGL: A Clonal Model for Polyclonal Responses

The Journal of immunology (1950), 2004-02, Vol.172 (3), p.1960-1969

2004

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Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia

Human heredity, 1998-01, Vol.48 (1), p.30-33

1998

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Evidence for genetic anticipation in hereditary non-polyposis colorectal cancer

Human genetics, 2005-05, Vol.116 (6), p.461-465

2005

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A de Novo PABPN1 Germline Mutation in a Patient with Oculopharyngeal Muscular Dystrophy

The Laryngoscope, 2006-01, Vol.116 (1), p.111-114

2006

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Expression of genes regulating angiogenesis in human circulating hematopoietic cord blood CD34+/CD133+ cells

European journal of haematology, 2003-03, Vol.70 (3), p.143-150

2003

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Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindred

European journal of human genetics : EJHG, 2004-05, Vol.12 (5), p.365-371

2004

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Diamond blackfan anemia stem cells fail to repopulate erythropoiesis in NOD/SCID mice

Blood cells, molecules, & diseases, 2003-07, Vol.31 (1), p.93-97

2003

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Genetic predisposition as a basis for chemoprevention, surgical and other interventions in colorectal cancer

Recent results in cancer research, 2003, Vol.163, p.235

2003

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TRAIL suppresses growth of primary human leukemia and myelodysplasia progenitors

Leukemia, 2002-01, Vol.16 (1), p.67

2002

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Mitochondria play a central role in apoptosis induced by a-tocopheryl succinate, an agent with antineoplastic activity: Comparison with receptor-mediated pro-apoptotic signaling

Biochemistry (Easton), 2003, Vol.42 (14), p.4277

2003

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2 clinico-genetic types of primary congenital glaucomas in Slovakia

Česká a slovenská oftalmologie, 1998, Vol.54 (5), p.289

1998

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Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma

Česká a slovenská oftalmologie, 1998, Vol.54 (5), p.281

1998

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Fahr´s Syndrome; Pseudohypoparathyroidism Type Ib Masquerading as Epileptic Seizures

Kathmandu University medical journal, 2022-12, Vol.20 (3), p.384-387

2022

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Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius

The journal of clinical endocrinology and metabolism, 2013-07, Vol.98 (7), p.E1241-E1247

2013

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The International Sexual Health And REproductive Health during COVID-19 (I-SHARE) Study: A Multicountry Analysis of Adults from 30 Countries Prior to and During the Initial Coronavirus Disease 2019 Wave

Clinical infectious diseases, 2022-08, Vol.75 (1), p.e991-e999

2022

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Fahr´s Syndrome; Pseudohypoparathyroidism Type Ib Masquerading as Epileptic Seizures

Kathmandu University medical journal, 2022-07, Vol.20 (79), p.384-387

2022

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Bone geometry and volumetric bone density at the radius in patients with isolated SHOX deficiency

Experimental and clinical endocrinology & diabetes, 2013-02, Vol.121 (2), p.109

2013

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NUP98 Dysregulation in Myeloid Leukemogenesis

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome

Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

TRAIL (Apo2l) suppresses growth of primary human leukemia and myelodysplasia progenitors

Shared and individual specificities of immunodominant cytotoxic T-cell clones in paroxysmal nocturnal hemoglobinuria as determined by molecular analysis

In-vivo dominant immune responses in aplastic anaemia: molecular tracking of putatively pathogenetic T-cell clones by TCR β-CDR3 sequencing

Mitochondria Play a Central Role in Apoptosis Induced by α-Tocopheryl Succinate, an Agent with Antineoplastic Activity: Comparison with Receptor-Mediated Pro-Apoptotic Signaling

Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers

Molecular Analysis of TCR Clonotypes in LGL: A Clonal Model for Polyclonal Responses

Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia

Evidence for genetic anticipation in hereditary non-polyposis colorectal cancer

A de Novo PABPN1 Germline Mutation in a Patient with Oculopharyngeal Muscular Dystrophy

Expression of genes regulating angiogenesis in human circulating hematopoietic cord blood CD34+/CD133+ cells

Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindred

Diamond blackfan anemia stem cells fail to repopulate erythropoiesis in NOD/SCID mice

Genetic predisposition as a basis for chemoprevention, surgical and other interventions in colorectal cancer

TRAIL suppresses growth of primary human leukemia and myelodysplasia progenitors

Mitochondria play a central role in apoptosis induced by a-tocopheryl succinate, an agent with antineoplastic activity: Comparison with receptor-mediated pro-apoptotic signaling

2 clinico-genetic types of primary congenital glaucomas in Slovakia

Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma

Fahr´s Syndrome; Pseudohypoparathyroidism Type Ib Masquerading as Epileptic Seizures

Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius

The International Sexual Health And REproductive Health during COVID-19 (I-SHARE) Study: A Multicountry Analysis of Adults from 30 Countries Prior to and During the Initial Coronavirus Disease 2019 Wave

Fahr´s Syndrome; Pseudohypoparathyroidism Type Ib Masquerading as Epileptic Seizures

Bone geometry and volumetric bone density at the radius in patients with isolated SHOX deficiency

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