UB Paderborn / Katalog / Suche / in CDI

1 – 16 von 16

Sortiert nach

Targeted exome sequencing in clear cell renal cell carcinoma tumors suggests aberrant chromatin regulation as a crucial step in ccRCC development

Human mutation, 2012-07, Vol.33 (7), p.1059-1062

2012

Link zum Volltext

Verfügbarkeit prüfen

Abstract 5335: Discovery and validation of new kinase targets for therapy in ovarian clear cell cancer

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.5335-5335

2015

Link zum Volltext

Verfügbarkeit prüfen

Systematic identification of tRNAome and its dynamics in L actococcus lactis

Molecular microbiology, 2014-09, Vol.93 (5), p.944-956

2014

Link zum Volltext

Verfügbarkeit prüfen

Differences in gene expression related to the results of obesity treatment, peak oxygen uptake and fatty acid metabolism measured in a cardiopulmonary exercise test

Polskie archiwum medycyny wewne̦trznej, 2018-03

2018

Link zum Volltext

Verfügbarkeit prüfen

Whole Blood Gene Expression Profiles of Patients with a Past Aneurysmal Subarachnoid Hemorrhage: e0139352

PloS one, 2015-10, Vol.10 (10)

2015

Link zum Volltext

Verfügbarkeit prüfen

Lessons Learned from Whole Exome Sequencing in Multiplex Families Affected by a Complex Genetic Disorder, Intracranial Aneurysm: e0121104

PloS one, 2015-03, Vol.10 (3)

2015

Link zum Volltext

Verfügbarkeit prüfen

Improvements in gel composition and electrophoretic conditions for broad-range mutation analysis by denaturing gradient gel electrophoresis

Nucleic acids research, 1999-10, Vol.27 (20), p.e29

1999

Link zum Volltext

Verfügbarkeit prüfen

research paper: High expression of calcium-binding proteins, S100A10, S100A11 and CALM2 in anaplastic large cell lymphoma

British journal of haematology, 2005-12, Vol.131 (5), p.596-608

2005

Link zum Volltext

Verfügbarkeit prüfen

P7: The application of a 6 K genome-wide BAC-array in clinical diagnostic

European journal of medical genetics, 2005-10, Vol.48 (4), p.452-453

2005

Link zum Volltext

Verfügbarkeit prüfen

From chromosomes to molecular karyotyping : Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation

European journal of medical genetics, 2005, Vol.48 (3), p.250-262

2005

Link zum Volltext

Verfügbarkeit prüfen

Close linkage of the Wilsons's disease locus to D13S12 in the chromosomal region 13q21 and not to ESD in 13q14

Human genetics, 1990-10, Vol.85 (5), p.560-562

1990

Link zum Volltext

Verfügbarkeit prüfen

FISH and array-CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions

American Journal of Medical Genetics Part A, 2006, Vol.140A (22), p.2482-2487

2006

Link zum Volltext

Verfügbarkeit prüfen

Detection of point mutation in dystrophin gene reveals somatic and germline mosaicism in the mother of a patient with Duchenne muscular dystrophy

American journal of medical genetics. Part A, 2003, Vol.118A (3), p.296-298

2003

Link zum Volltext

Verfügbarkeit prüfen

Molecular analysis of renal cell carcinoma

Cancer genetics and cytogenetics, 1991-04, Vol.52 (2), p.244-244

1991

Link zum Volltext

Verfügbarkeit prüfen

Même Dying Stop Confirm Arrival Stop: Provincial Literatures in Global Time—The Case of Marlene van Niekerk's Agaat 1

Institutions of World Literature, 2016, p.191-208

1, 2016

Link zum Volltext

Verfügbarkeit prüfen

1 – 16 von 16

Suche als RSS-Feed

Aktive Filter

ThemaScience & Technology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(12)
Mit Volltextzugriff
(15)

Publikationsform

Sprache

Englisch
(16)
Japanisch
(1)

Erscheinungsjahr

n.n

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Targeted exome sequencing in clear cell renal cell carcinoma tumors suggests aberrant chromatin regulation as a crucial step in ccRCC development

Abstract 5335: Discovery and validation of new kinase targets for therapy in ovarian clear cell cancer

Systematic identification of tRNAome and its dynamics in L actococcus lactis

Combining Genome Wide Association Study and lung eQTL analysis provides evidence for novel genes associated with asthma

Differences in gene expression related to the results of obesity treatment, peak oxygen uptake and fatty acid metabolism measured in a cardiopulmonary exercise test

Whole Blood Gene Expression Profiles of Patients with a Past Aneurysmal Subarachnoid Hemorrhage: e0139352

Lessons Learned from Whole Exome Sequencing in Multiplex Families Affected by a Complex Genetic Disorder, Intracranial Aneurysm: e0121104

Improvements in gel composition and electrophoretic conditions for broad-range mutation analysis by denaturing gradient gel electrophoresis

research paper: High expression of calcium-binding proteins, S100A10, S100A11 and CALM2 in anaplastic large cell lymphoma

P7: The application of a 6 K genome-wide BAC-array in clinical diagnostic

From chromosomes to molecular karyotyping : Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation

Close linkage of the Wilsons's disease locus to D13S12 in the chromosomal region 13q21 and not to ESD in 13q14

FISH and array-CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions

Detection of point mutation in dystrophin gene reveals somatic and germline mosaicism in the mother of a patient with Duchenne muscular dystrophy

Molecular analysis of renal cell carcinoma

Même Dying Stop Confirm Arrival Stop: Provincial Literatures in Global Time—The Case of Marlene van Niekerk's Agaat 1

Aktive Filter

Suchergebnisse filtern