UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 151

Sortiert nach

Relationship between chromosomal aberrations and gene expressions in the p53 pathway in chronic lymphocytic leukemia

Balkan journal of medical genetics, 2020-08, Vol.23 (1), p.15-24

2020

Volltextzugriff (PDF)

Investigation of mutations in the synaptonemal complex protein 3 (SYCP3) gene among azoospermic infertile male patients in the Turkish population

Andrologia, 2013-04, Vol.45 (2), p.92-100

2013

Volltextzugriff (PDF)

The frequency of C609T polymorphism in the NQO1 gene and its relation to cytogenetic abnormalities in patients with myelodysplastic syndrome

Cellular and molecular biology (Noisy-le-Grand, France), 2016-06, Vol.62 (7), p.61

2016

Volltextzugriff (PDF)

Monitoring the genotoxic effects of radiosynovectomy with Re-186 in paediatric age group undergoing therapy for haemophilic synovitis

Haemophilia : the official journal of the World Federation of Hemophilia, 2007-01, Vol.13 (1), p.57-64

2007

Volltextzugriff (PDF)

OXIDANT AND ANTIOXIDANT SYSTEMS IN NIDDM PATIENTS: INFLUENCE OF VITAMIN E SUPPLEMENTATION

Endocrine research, 2001-01, Vol.27 (3), p.377-386

2001

Volltextzugriff (PDF)

Initial maternal meiotic I error leading to the formation of a maternal i(2q) and a paternal i(2p) in a healthy male

Cytogenetic and genome research, 2007-01, Vol.118 (1), p.38-41

2007

Volltextzugriff (PDF)

Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction

Gastroenterology (New York, N.Y. 1943), 2015-04, Vol.148 (4), p.771-782.e11

2015

Volltextzugriff (PDF)

A study of serological markers of hepatitis B and C viruses in Istanbul, Turkey

Medical principles and practice, 2003-07, Vol.12 (3), p.184

2003

Volltextzugriff (PDF)

Evaluation of micronuclear frequencies in both circulating lymphocytes and buccal epithelial cells of patients with oral lichen planus and oral lichenoid contact reactions

Oral diseases, 2014-07, Vol.20 (5), p.521-527

2014

Volltextzugriff (PDF)

A case of progressive pseudorheumatoid arthropathy of ‘childhood’ with the diagnosis delayed to the fifth decade

International journal of clinical practice (Esher), 2006-10, Vol.60 (10), p.1306-1309

2006

Volltextzugriff (PDF)

Two siblings with distal pachydermodactyly

Clinical and experimental dermatology, 2005-11, Vol.30 (6), p.707-709

2005

Volltextzugriff (PDF)

Plasma antioxidants and type 2 diabetes mellitus

Research communications in molecular pathology and pharmacology, 2001, Vol.109 (5-6), p.309

2001

Volltextzugriff (PDF)

Micronuclear and sister chromatid exchange analyses in peripheral lymphocytes of patients with oral lichen planus - a pilot study

Oral diseases, 2009-10, Vol.15 (7), p.499-504

2009

Volltextzugriff (PDF)

The role of HLA antigens in chronic hepatitis B virus infection

Journal of the Pakistan Medical Association, 2002-06, Vol.52 (6), p.253-256

2002

Volltextzugriff (PDF)

CHRONIC RENAL FAILURE IN A PATIENT WITH SOTOS SYNDROME DUE TO AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

International journal of clinical practice (Esher), 2002-05, Vol.56 (4), p.316-318

2002

Volltextzugriff (PDF)

Investigation of Arg399Gln and Arg194Trp polymorphisms of the XRCC1 (x-ray cross-complementing group 1) gene and its correlation to sister chromatid exchange frequency in patients with chronic lymphocytic leukemia

Genetic testing and molecular biomarkers, 2012-04, Vol.16 (4), p.287

2012

Volltextzugriff (PDF)

Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes

European journal of human genetics : EJHG, 2003-11, Vol.11 (11), p.858-865

2003

Volltextzugriff (PDF)

Brucellosis in a mother and her young infant: Probable transmission by breast milk

International journal of infectious diseases, 2000, Vol.4 (1), p.55-56

2000

Volltextzugriff (PDF)

Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus

Medicina oral, patología oral y cirugía bucal, 2018-03, Vol.23 (2), p.e144-e150

2018

Volltextzugriff (PDF)

Vitamin E and ATPases : Protection of ATPase activities by vitamin E supplementation in various tissues of hypercholesterolemic rats

International journal for vitamin and nutrition research, 2000, Vol.70 (1), p.3-7

2000

Volltextzugriff (PDF)

Effect of cyclosporin A and tacrolimus on sister chromatid exchange frequency in renal transplant patients

Genetic testing, 2008-09, Vol.12 (3), p.427

2008

Volltextzugriff (PDF)

Brachydactyly type C caused by a homozygous missense mutation in the prodomain of CDMP1

American journal of medical genetics, 2004-02, Vol.124A (4), p.356-363

2004

Volltextzugriff (PDF)

A case of progressive pseudorheumatoid arthropathy of ‘childhood’ with the diagnosis delayed to the fifth decade: A CASE OF PROGRESSIVE PSEUDORHEUMATOID ARTHROPATHY

International journal of clinical practice (Esher), 2006-10, Vol.60 (10), p.1306-1309

2006

Volltextzugriff (PDF)

CASE REPORT: A case of progressive pseudorheumatoid arthropathy of 'childhood' with the diagnosis delayed to the fifth decade

International journal of clinical practice (Esher), 2006-10, Vol.60 (10), p.1306

2006

Volltextzugriff (PDF)

The genotoxic effects in lymphocyte cultures of children treated with radiosynovectomy by using yttrium-90 citrate colloid

Cancer biotherapy & radiopharmaceuticals, 2007-06, Vol.22 (3), p.393

2007

Volltextzugriff (PDF)

1 – 25 von 151

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(123)
Mit Volltextzugriff
(124)

Publikationsform

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Relationship between chromosomal aberrations and gene expressions in the p53 pathway in chronic lymphocytic leukemia

Investigation of mutations in the synaptonemal complex protein 3 (SYCP3) gene among azoospermic infertile male patients in the Turkish population

The frequency of C609T polymorphism in the NQO1 gene and its relation to cytogenetic abnormalities in patients with myelodysplastic syndrome

Monitoring the genotoxic effects of radiosynovectomy with Re-186 in paediatric age group undergoing therapy for haemophilic synovitis

OXIDANT AND ANTIOXIDANT SYSTEMS IN NIDDM PATIENTS: INFLUENCE OF VITAMIN E SUPPLEMENTATION

Initial maternal meiotic I error leading to the formation of a maternal i(2q) and a paternal i(2p) in a healthy male

Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction

A study of serological markers of hepatitis B and C viruses in Istanbul, Turkey

Evaluation of micronuclear frequencies in both circulating lymphocytes and buccal epithelial cells of patients with oral lichen planus and oral lichenoid contact reactions

A case of progressive pseudorheumatoid arthropathy of ‘childhood’ with the diagnosis delayed to the fifth decade

Two siblings with distal pachydermodactyly

Plasma antioxidants and type 2 diabetes mellitus

Micronuclear and sister chromatid exchange analyses in peripheral lymphocytes of patients with oral lichen planus - a pilot study

The role of HLA antigens in chronic hepatitis B virus infection

CHRONIC RENAL FAILURE IN A PATIENT WITH SOTOS SYNDROME DUE TO AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

Investigation of Arg399Gln and Arg194Trp polymorphisms of the XRCC1 (x-ray cross-complementing group 1) gene and its correlation to sister chromatid exchange frequency in patients with chronic lymphocytic leukemia

Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes

Brucellosis in a mother and her young infant: Probable transmission by breast milk

Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus

Vitamin E and ATPases : Protection of ATPase activities by vitamin E supplementation in various tissues of hypercholesterolemic rats

Effect of cyclosporin A and tacrolimus on sister chromatid exchange frequency in renal transplant patients

Brachydactyly type C caused by a homozygous missense mutation in the prodomain of CDMP1

A case of progressive pseudorheumatoid arthropathy of ‘childhood’ with the diagnosis delayed to the fifth decade: A CASE OF PROGRESSIVE PSEUDORHEUMATOID ARTHROPATHY

CASE REPORT: A case of progressive pseudorheumatoid arthropathy of 'childhood' with the diagnosis delayed to the fifth decade

The genotoxic effects in lymphocyte cultures of children treated with radiosynovectomy by using yttrium-90 citrate colloid

Suchergebnisse filtern