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Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders

Epigenetics, 2018-09, Vol.13 (9), p.897-909

2018

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Blood fetal microchimerism in primary biliary cirrhosis

Clinical and experimental immunology, 2000-12, Vol.122 (3), p.418-422

2000

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ESX1 gene expression as a robust marker of residual spermatogenesis in azoospermic men

Human reproduction (Oxford), 2010-06, Vol.25 (6), p.1398-1403

2010

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Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies

Placenta (Eastbourne), 2005, Vol.26 (1), p.10-18

2005

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Endogenous Reactivation of the RAR beta 2 Tumor Suppressor Gene Epigenetically Silenced in Breast Cancer

Cancer research (Chicago, Ill.), 2002-05, Vol.62 (9), p.2455-2461

2002

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Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor beta 2 promoter in breast cancer cells

Oncogene, 2000-03, Vol.19 (12), p.1556-1563

2000

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Confined placental mosaicism

Prenatal diagnosis, 1994-12, Vol.14 (13), p.1185-1189

1994

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Emotion‐Induced Myoclonic Absence‐Like Seizures in a Patient with Inv‐Dup(15) Syndrome: A Clinical, EEG, and Molecular Genetic Study

Epilepsia (Copenhagen), 1999-09, Vol.40 (9), p.1316-1319

1999

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Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism

Prenatal diagnosis, 1998-03, Vol.18 (3), p.201-206

1998

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Highly sensitive chemiluminescent method for the detection of maternal cell contamination in human cord blood stored for allotransplantation: the experience of the Milano cord blood bank

Blood, 1997-04, Vol.89 (8), p.3061-3061

1997

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ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men

Human reproduction (Oxford), 2014-12, Vol.29 (12), p.2620-2627

2014

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Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotype

Human genetics, 1994-10, Vol.94 (4), p.355-358

1994

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Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected

AIDS (London), 1997-05, Vol.11 (6), p.840-841

1997

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Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries

Atherosclerosis, 2001-12, Vol.159 (2), p.261-267

2001

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Characterization of four microsatellites in an Italian population and their application to paternity testing

Molecular and cellular probes, 1996-04, Vol.10 (2), p.155-158

1996

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Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor β2 promoter in breast cancer cells

Oncogene, 2000-03, Vol.19 (12), p.1556-1563

2000

Volltextzugriff (PDF)

The Methylation of the TSC2 Promoter Underlies the Abnormal Growth of TSC2 Angiomyolipoma-Derived Smooth Muscle Cells

The American journal of pathology, 2009-06, Vol.174 (6), p.2150-2159

2009

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Highly sensitive chemiluminescent method for the detection of cell contamination

Journal of bioluminescence and chemiluminescence, 1998-09, Vol.13 (5), p.303-305

1998

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A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome

American journal of medical genetics. Part A, 2018-06, Vol.176 (6), p.1427-1431

2018

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Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery

AIDS (London), 2000-03, Vol.14 (5), p.623-625

2000

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Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells

Cancer research (Chicago, Ill.), 2005-03, Vol.65 (6), p.2139-2146

2005

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Losses of Heterozygosity in Oral and Oropharyngeal Epithelial Carcinomas

Cancer genetics and cytogenetics, 2000-04, Vol.118 (1), p.57-61

2000

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ESXI gene expression as a robust marker of residual spermatogenesis in azoospermic men

Human reproduction (Oxford), 2010, Vol.25 (6), p.1398-1403

2010

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Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected

AIDS (London), 1997-07, Vol.11 (8), p.840-841

1997

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Aneuploid correction and confined placental mosaicism

Acta geneticae medicae et gemellologiae, 1996, Vol.45 (1-2), p.153

1996

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Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders

Blood fetal microchimerism in primary biliary cirrhosis

ESX1 gene expression as a robust marker of residual spermatogenesis in azoospermic men

Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies

Endogenous Reactivation of the RAR beta 2 Tumor Suppressor Gene Epigenetically Silenced in Breast Cancer

Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor beta 2 promoter in breast cancer cells

Confined placental mosaicism

Emotion‐Induced Myoclonic Absence‐Like Seizures in a Patient with Inv‐Dup(15) Syndrome: A Clinical, EEG, and Molecular Genetic Study

Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism

Highly sensitive chemiluminescent method for the detection of maternal cell contamination in human cord blood stored for allotransplantation: the experience of the Milano cord blood bank

ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men

Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotype

Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected

Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries

Characterization of four microsatellites in an Italian population and their application to paternity testing

Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor β2 promoter in breast cancer cells

The Methylation of the TSC2 Promoter Underlies the Abnormal Growth of TSC2 Angiomyolipoma-Derived Smooth Muscle Cells

Highly sensitive chemiluminescent method for the detection of cell contamination

A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome

Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery

Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells

Losses of Heterozygosity in Oral and Oropharyngeal Epithelial Carcinomas

ESXI gene expression as a robust marker of residual spermatogenesis in azoospermic men

Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected

Aneuploid correction and confined placental mosaicism

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