UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Foxl2 is required for commitment to ovary differentiation

Human molecular genetics, 2005-07, Vol.14 (14), p.2053-2062

2005

Volltextzugriff (PDF)

Heritability of cardiovascular and personality traits in 6,148 Sardinians

PLoS genetics, 2006-08, Vol.2 (8), p.e132-e132

2006

Volltextzugriff (PDF)

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

Nature genetics, 2001-02, Vol.27 (2), p.159-166

2001

Volltextzugriff (PDF)

Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28

Nature genetics, 2000-07, Vol.25 (3), p.324-328

2000

Volltextzugriff (PDF)

Aging of Oocyte, Ovary, and Human Reproduction

Annals of the New York Academy of Sciences, 2004-12, Vol.1034 (1), p.117-131

2004

Volltextzugriff (PDF)

Mutations in GPC3 , a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

Nature genetics, 1996-03, Vol.12 (3), p.241-247

1996

Volltextzugriff (PDF)

X-linked situs abnormalities result from mutations in ZIC3

Nature genetics, 1997-11, Vol.17 (3), p.305-308

1997

Volltextzugriff (PDF)

Overgrowth of a Mouse Model of the Simpson–Golabi–Behmel Syndrome Is Independent of IGF Signaling

Developmental biology, 2002-03, Vol.243 (1), p.185-206

2002

Volltextzugriff (PDF)

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

Human molecular genetics, 2004-06, Vol.13 (11), p.1171-1181

2004

Volltextzugriff (PDF)

DNA Methylation in Transcriptional Repression of Two Differentially Expressed X-Linked Genes, GPC3 and SYBL1

Proceedings of the National Academy of Sciences - PNAS, 1999-01, Vol.96 (2), p.616-621

1999

Volltextzugriff (PDF)

IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma

American journal of human genetics, 2007-06, Vol.80 (6), p.1103-1114

2007

Volltextzugriff (PDF)

Isochores and CpG Islands in YAC Contigs in Human Xq26.1-qter

Genomics (San Diego, Calif.), 1993-08, Vol.17 (2), p.456-462

1993

Volltextzugriff (PDF)

Analysis of Exon/Intron Structure and 400 kb of Genomic Sequence Surrounding the 5′-Promoter and 3′-Terminal Ends of the Human Glypican 3 (GPC3) Gene

Genomics (San Diego, Calif.), 1997-10, Vol.45 (1), p.48-58

1997

Volltextzugriff (PDF)

FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences

Genomics (San Diego, Calif.), 2004-05, Vol.83 (5), p.757-764

2004

Volltextzugriff (PDF)

Genes and translocations involved in POF

American journal of medical genetics, 2002-08, Vol.111 (3), p.328-333

2002

Volltextzugriff (PDF)

Personality traits in Sardinia: testing founder population effects on trait means and variances

Behavior genetics, 2007-03, Vol.37 (2), p.376-387

2007

Volltextzugriff (PDF)

Gpc3 expression correlates with the phenotype of the Simpson‐Golabi‐Behmel syndrome

Developmental dynamics, 1998-12, Vol.213 (4), p.431-439

1998

Volltextzugriff (PDF)

X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content

Genome research, 1997-03, Vol.7 (3), p.210-222

1997

Volltextzugriff (PDF)

FoxI2 is required for commitment to ovary differentiation

Human molecular genetics, 2005, Vol.14 (14), p.2053-2062

2005

Volltextzugriff (PDF)

Detection of deletion mutations extending beyond the HPRT gene by multiplex PCR analysis

Somatic cell and molecular genetics, 1994-01, Vol.20 (1), p.39-46

1994

Volltextzugriff (PDF)

Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome: Clinical and Molecular Analysis of a Case

Journal of AAPOS, 2006-06, Vol.10 (3), p.279-280

2006

Volltextzugriff (PDF)

A Submicroscopic Deletion in Xq26 Associated with Familial Situs Ambiguus

American journal of human genetics, 1997-08, Vol.61 (2), p.395-401

1997

Volltextzugriff (PDF)

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome

Journal of medical genetics, 1997-06, Vol.34 (6), p.480-483

1997

Volltextzugriff (PDF)

FoxI2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

Human molecular genetics, 2004, Vol.13 (11), p.1171-1181

2004

Volltextzugriff (PDF)

Recombination trapping: an in-vivo approach to recover cDNAs encoded in YACs

Gene, 1998-06, Vol.212 (2), p.315-321

1998

Volltextzugriff (PDF)

1 – 25 von 79

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(70)
Mit Volltextzugriff
(69)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(58)
Life Sciences & Biomedicine
(47)
Humans
(44)
Genetics & Heredity
(28)
Biological And Medical Sciences
(26)
Female
(26)
Male
(20)
Fundamental And Applied Biological Sciences. Psychology
(17)
Molecular Sequence Data
(16)
Animals
(13)
Base Sequence
(13)
X Chromosome
(13)
Medical Sciences
(12)
Chromosome Mapping
(11)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(11)
Middle Aged
(11)
Adult
(10)
Biotechnology & Applied Microbiology
(10)
Genes
(10)
Molecular And Cellular Biology
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Foxl2 is required for commitment to ovary differentiation

Heritability of cardiovascular and personality traits in 6,148 Sardinians

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28

Aging of Oocyte, Ovary, and Human Reproduction

Mutations in GPC3 , a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

X-linked situs abnormalities result from mutations in ZIC3

Overgrowth of a Mouse Model of the Simpson–Golabi–Behmel Syndrome Is Independent of IGF Signaling

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

DNA Methylation in Transcriptional Repression of Two Differentially Expressed X-Linked Genes, GPC3 and SYBL1

IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma

Isochores and CpG Islands in YAC Contigs in Human Xq26.1-qter

Analysis of Exon/Intron Structure and 400 kb of Genomic Sequence Surrounding the 5′-Promoter and 3′-Terminal Ends of the Human Glypican 3 (GPC3) Gene

FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences

Genes and translocations involved in POF

Personality traits in Sardinia: testing founder population effects on trait means and variances

Gpc3 expression correlates with the phenotype of the Simpson‐Golabi‐Behmel syndrome

X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content

FoxI2 is required for commitment to ovary differentiation

Detection of deletion mutations extending beyond the HPRT gene by multiplex PCR analysis

Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome: Clinical and Molecular Analysis of a Case

A Submicroscopic Deletion in Xq26 Associated with Familial Situs Ambiguus

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome

FoxI2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

Recombination trapping: an in-vivo approach to recover cDNAs encoded in YACs

Suchergebnisse filtern