UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 314

Sortiert nach

Identification of WTAP, a novel Wilms' tumour 1-associating protein

Human molecular genetics, 2000-09, Vol.9 (15), p.2231-2239

2000

Volltextzugriff (PDF)

Estimating Human Inbreeding Coefficients: Comparison of Genealogical and Marker Heterozygosity Approaches

Annals of human genetics, 2006-09, Vol.70 (5), p.666-676

2006

Volltextzugriff (PDF)

Calcium/NFAT signalling promotes early nephrogenesis

Developmental biology, 2011-04, Vol.352 (2), p.288-298

2011

Volltextzugriff (PDF)

Wt1 and retinoic acid signaling are essential for stellate cell development and liver morphogenesis

Developmental biology, 2007-12, Vol.312 (1), p.157-170

2007

Volltextzugriff (PDF)

Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways

Journal of medical genetics, 2011-06, Vol.48 (6), p.369-374

2011

Volltextzugriff (PDF)

The Genetics of Wilms' Tumor-A Case of Disrupted Development

Annual review of genetics, 1994-01, Vol.28 (1), p.523-558

Hastie, N D

1994

Volltextzugriff (PDF)

Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerations

Human molecular genetics, 2004-01, Vol.13 (1), p.25-33

2004

Volltextzugriff (PDF)

Mouse Small eye results from mutations in a paired-like homeobox-containing gene

Nature (London), 1991-12, Vol.354 (6354), p.522-525

1991

Volltextzugriff (PDF)

RNA Binding by the Wilms Tumor Suppressor Zinc Finger Proteins

Proceedings of the National Academy of Sciences - PNAS, 1996-07, Vol.93 (15), p.7562-7566

1996

Volltextzugriff (PDF)

Telomere reduction in human colorectal carcinoma and with ageing

Nature (London), 1990-08, Vol.346 (6287), p.866-868

1990

Volltextzugriff (PDF)

Modulation of DNA Binding Specificity by Alternative Splicing of the Wilms Tumor wt1 Gene Transcript

Science (American Association for the Advancement of Science), 1992-07, Vol.257 (5067), p.235-237

1992

Volltextzugriff (PDF)

Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations

Heredity, 2016-03, Vol.116 (3), p.333-338

2016

Volltextzugriff (PDF)

Zinc Finger Point Mutations Within the WT1 Gene in Wilms Tumor Patients

Proceedings of the National Academy of Sciences - PNAS, 1992-06, Vol.89 (11), p.4791-4795

1992

Volltextzugriff (PDF)

Defective mitosis due to a mutation in the gene for a fission yeast 26S protease subunit

Nature (London), 1993-11, Vol.366 (6453), p.355-357

1993

Volltextzugriff (PDF)

Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papilla

Human molecular genetics, 2011-03, Vol.20 (5), p.917-926

2011

Volltextzugriff (PDF)

YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis

Development (Cambridge), 1999-05, Vol.126 (9), p.1845-1857

1999

Volltextzugriff (PDF)

Life, Sex, and WT1 Isoforms— Three Amino Acids Can Make All the Difference

Cell, 2001-08, Vol.106 (4), p.391-394

Hastie, Nicholas D.

2001

Volltextzugriff (PDF)

The Wilms' tumour protein (WT1) shuttles between nucleus and cytoplasm and is present in functional polysomes

Human molecular genetics, 2004-02, Vol.13 (4), p.463-471

2004

Volltextzugriff (PDF)

Transcriptome analysis of human autosomal trisomy

Human molecular genetics, 2002-12, Vol.11 (26), p.3249-3256

2002

Volltextzugriff (PDF)

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration

Human molecular genetics, 2003-10, Vol.12 (20), p.2657-2667

2003

Volltextzugriff (PDF)

Extensive telomere repeat arrays in mouse are hypervariable

Nucleic acids research, 1990-12, Vol.18 (23), p.6881-6888

1990

Volltextzugriff (PDF)

Influence of PAX6 Gene Dosage on Development: Overexpression Causes Severe Eye Abnormalities

Cell, 1996-07, Vol.86 (1), p.71-82

1996

Volltextzugriff (PDF)

Cross-talk in kidney development

Current Opinion in Genetics & Development, 2000-10, Vol.10 (5), p.543-549

2000

Volltextzugriff (PDF)

The Wilms’ tumor suppressor WT1: Approaches to gene function

Kidney international, 1998-06, Vol.53 (6), p.1512-1518

1998

Volltextzugriff (PDF)

Gonadal effects of a mouse Denys-Drash Syndrome mutation

Transgenic research, 2005-10, Vol.14 (5), p.691-702

2005

Volltextzugriff (PDF)

1 – 25 von 314

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(294)
Mit Volltextzugriff
(289)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(216)
Life Sciences & Biomedicine
(174)
Humans
(144)
Animals
(97)
Male
(85)
Female
(71)
Biological And Medical Sciences
(70)
Mice
(68)
Genetics & Heredity
(54)
Fundamental And Applied Biological Sciences. Psychology
(52)
Biochemistry & Molecular Biology
(43)
Middle Aged
(39)
Respiratory System
(37)
Adult
(35)
Base Sequence
(30)
Cell Biology
(30)
General & Internal Medicine
(30)
Asthma
(29)
Medical Sciences
(29)
Medicin Och Hälsovetenskap
(29)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Identification of WTAP, a novel Wilms' tumour 1-associating protein

Estimating Human Inbreeding Coefficients: Comparison of Genealogical and Marker Heterozygosity Approaches

Calcium/NFAT signalling promotes early nephrogenesis

Wt1 and retinoic acid signaling are essential for stellate cell development and liver morphogenesis

Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways

The Genetics of Wilms' Tumor-A Case of Disrupted Development

Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerations

Mouse Small eye results from mutations in a paired-like homeobox-containing gene

RNA Binding by the Wilms Tumor Suppressor Zinc Finger Proteins

Telomere reduction in human colorectal carcinoma and with ageing

Modulation of DNA Binding Specificity by Alternative Splicing of the Wilms Tumor wt1 Gene Transcript

Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations

Zinc Finger Point Mutations Within the WT1 Gene in Wilms Tumor Patients

Defective mitosis due to a mutation in the gene for a fission yeast 26S protease subunit

Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papilla

YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis

Life, Sex, and WT1 Isoforms— Three Amino Acids Can Make All the Difference

The Wilms' tumour protein (WT1) shuttles between nucleus and cytoplasm and is present in functional polysomes

Transcriptome analysis of human autosomal trisomy

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration

Extensive telomere repeat arrays in mouse are hypervariable

Influence of PAX6 Gene Dosage on Development: Overexpression Causes Severe Eye Abnormalities

Cross-talk in kidney development

The Wilms’ tumor suppressor WT1: Approaches to gene function

Gonadal effects of a mouse Denys-Drash Syndrome mutation

Suchergebnisse filtern