UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 516

Sortiert nach

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

Volltextzugriff (PDF)

OTX1 expression in breast cancer is regulated by p53

Oncogene, 2011-07, Vol.30 (27), p.3096-3103

2011

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

OTX1 expression in breast cancer is regulated by p53

Oncogene, 2014-03, Vol.33 (10), p.1340-1340

2014

Volltextzugriff (PDF)

Blood fetal microchimerism in primary biliary cirrhosis

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

2000

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Placental IGF2 Expression in Normal and Intrauterine Growth Restricted (IUGR) Pregnancies

Placenta (Eastbourne), 2008-01, Vol.29 (1), p.99-101

2008

Volltextzugriff (PDF)

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

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

2005

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Confined placental mosaicism

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

1994

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH)

European journal of endocrinology, 2018-01, Vol.178 (1), p.23

2018

Volltextzugriff (PDF)

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

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

1998

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Erratum: OTX1 expression in breast cancer is regulated by p53

Oncogene, 2014-03, Vol.33 (10), p.1340-1340

2014

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

The challenges of measuring bleeding outcomes in clinical trials of platelet transfusions

Transfusion (Philadelphia, Pa.), 2013-07, Vol.53 (7), p.1531-1543

2013

Volltextzugriff (PDF)

OTX1 expression in breast cancer is regulated by p53

Oncogene, 2011-07, Vol.30 (27), p.3104-3104

2011

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

1 – 25 von 516

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieBlood

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(432)
Mit Volltextzugriff
(313)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(352)
Science & Technology
(310)
Life Sciences & Biomedicine
(296)
Female
(154)
Biological And Medical Sciences
(122)
Male
(114)
Medical Sciences
(111)
Hematology
(110)
Adult
(98)
Middle Aged
(64)
Immunology
(57)
Anesthesia. Intensive Care Medicine. Transfusions. Cell Therapy And Gene Therapy
(44)
Adolescent
(42)
Genetics & Heredity
(42)
Italy
(41)
Transfusions. Complications. Transfusion Reactions. Cell And Gene Therapy
(41)
Transplantation
(41)
Child
(35)
Surgery
(33)
Aged
(32)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Vox Sanguinis
(51)
Transfusion
(41)
Transplantation Proceedings
(26)
British Journal Of Haematology
(22)
Tissue Antigens
(16)
Haematologica
(12)
Transplant International
(11)
Bone Marrow Transplantation
(9)
Oncogene
(9)
American Journal Of Medical Genetics. Part A
(7)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

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

OTX1 expression in breast cancer is regulated by p53

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

OTX1 expression in breast cancer is regulated by p53

Blood fetal microchimerism in primary biliary cirrhosis

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

Placental IGF2 Expression in Normal and Intrauterine Growth Restricted (IUGR) Pregnancies

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

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

Confined placental mosaicism

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

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

Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH)

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

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

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

Erratum: OTX1 expression in breast cancer is regulated by p53

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

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

The challenges of measuring bleeding outcomes in clinical trials of platelet transfusions

OTX1 expression in breast cancer is regulated by p53

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

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

Aktive Filter

Suchergebnisse filtern