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...

The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic ( oc/oc) mutants

Bone (New York, N.Y.), 2000-03, Vol.26 (3), p.207-213

2000

Volltextzugriff (PDF)

Segmental duplications in euchromatic regions of human chromosome 5: a source of evolutionary instability and transcriptional innovation

Genome research, 2003-03, Vol.13 (3), p.369-381

2003

Volltextzugriff (PDF)

Detailed map of a region commonly amplified at 11q13-->q14 in human breast carcinoma

Cytogenetic and genome research, 1997-01, Vol.79 (1-2), p.125-131

1997

Volltextzugriff (PDF)

Menin interacting proteins as clues toward the understanding of multiple endocrine neoplasia type 1

Cancer Letters, 2003-01, Vol.189 (1), p.1-10

2003

Volltextzugriff (PDF)

Distinct MDM2 and P14ARF expression and centrosome amplification in well-differentiated liposarcomas

Genes chromosomes & cancer, 2004-02, Vol.39 (2), p.99-109

2004

Volltextzugriff (PDF)

BEK and FLG, two receptors to members of the FGF family, are amplified in subsets of human breast cancers

Oncogene, 1991-04, Vol.6 (4), p.659-663

1991

Volltextzugriff (PDF)

Three-dimensional culture and differentiation of human osteogenic cells in an injectable hydroxypropylmethylcellulose hydrogel

Biomaterials, 2005-09, Vol.26 (27), p.5509-5517

2005

Volltextzugriff (PDF)

Proto-oncogene amplification and human breast tumor phenotype

Oncogene, 1989-11, Vol.4 (11), p.1389-1395

1989

Volltextzugriff (PDF)

Deregulation of genetic pathways in neuroendocrine tumors

Annals of oncology, 2001, Vol.12 (suppl-2), p.S3-S11

2001

Volltextzugriff (PDF)

Double minute chromosomes can be produced from precursors derived from a chromosomal deletion

Molecular and Cellular Biology, 1988-04, Vol.8 (4), p.1525-1533

1988

Volltextzugriff (PDF)

Amplification of FGF-related genes in human tumors: possible involvement of HST in breast carcinomas

Oncogene, 1989-07, Vol.4 (7), p.915-922

1989

Volltextzugriff (PDF)

Identification of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene

Human molecular genetics, 1997-07, Vol.6 (7), p.1177-1183

1997

Volltextzugriff (PDF)

Differential expression of multiple alternative spliceforms of the Men1 tumor suppressor gene in mouse

International journal of molecular medicine, 2001-12, Vol.8 (6), p.681

2001

Volltextzugriff (PDF)

Mapping genes according to their amplification status in tumor cells : contribution to the map of 11q13

Genomics (San Diego, Calif.), 1993-06, Vol.16 (3), p.745-750

1993

Volltextzugriff (PDF)

Characterization of the region of the short arm of chromosome 8 amplified in breast carcinoma

Oncogene, 1995-03, Vol.10 (5), p.995-1001

1995

Volltextzugriff (PDF)

The DNA mismatch-repair MLH3 protein interacts with MSH4 in meiotic cells, supporting a role for this MutL homolog in mammalian meiotic recombination

Human molecular genetics, 2002-07, Vol.11 (15), p.1697-1706

2002

Volltextzugriff (PDF)

Characterization of the mouse Men1 gene and its expression during development

Oncogene, 1998-11, Vol.17 (19), p.2485-2493

1998

Volltextzugriff (PDF)

Characterization of an episome produced in hamster cells that amplify a transfected CAD gene at high frequency: functional evidence for a mammalian replication origin

Molecular and Cellular Biology, 1987-05, Vol.7 (5), p.1740-1750

1987

Volltextzugriff (PDF)

FCER1B, a candidate gene for atopy, is located in 11q13 between CD20 and TCN1

Genomics (San Diego, Calif.), 1994-01, Vol.19 (2), p.399-400

1994

Volltextzugriff (PDF)

Germ-Line Mutation Analysis in Patients with Multiple Endocrine Neoplasia Type 1 and Related Disorders

American journal of human genetics, 1998-08, Vol.63 (2), p.455-467

1998

Volltextzugriff (PDF)

Experimental assessment of the detection limit of genomic amplification by comparative genomic hybridization CGH

Cytogenetic and genome research, 1997, Vol.78 (1), p.65-68

1997

Volltextzugriff (PDF)

Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996

Cytogenetic and genome research, 1996, Vol.74 (1-2), p.1-20

1996

Volltextzugriff (PDF)

Functional Characterization of a Promoter Region in the Human MEN1 Tumor Suppressor Gene

Journal of molecular biology, 2003-10, Vol.333 (1), p.87-102

2003

Volltextzugriff (PDF)

Novel mutations in the TCIRG1 gene encoding the a3 subunit of the vacuolar proton pump in patients affected by infantile malignant osteopetrosis

Human mutation, 2003-02, Vol.21 (2), p.151-157

2003

Volltextzugriff (PDF)

The search for the MEN1 gene

Journal of internal medicine, 1998-06, Vol.243 (6), p.441-446

1998

Volltextzugriff (PDF)

1 – 25 von 120

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(97)
Mit Volltextzugriff
(91)

Publikationsform

Sprache

Englisch
(107)
Französisch
(13)

Erscheinungsjahr

n.n

Thema

Humans
(70)
Science & Technology
(69)
Life Sciences & Biomedicine
(67)
Biological And Medical Sciences
(41)
Genetics & Heredity
(41)
Animals
(33)
Chromosomes, Human, Pair 11
(31)
Chromosome Mapping
(29)
Biochemistry & Molecular Biology
(25)
Female
(25)
Medical Sciences
(22)
In Situ Hybridization, Fluorescence
(21)
Fundamental And Applied Biological Sciences. Psychology
(20)
Oncology
(20)
Gene Amplification
(19)
Male
(17)
Medicin Och Hälsovetenskap
(17)
Mice
(17)
Breast Neoplasms - Genetics
(15)
Cell Biology
(15)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic ( oc/oc) mutants

Segmental duplications in euchromatic regions of human chromosome 5: a source of evolutionary instability and transcriptional innovation

Detailed map of a region commonly amplified at 11q13-->q14 in human breast carcinoma

Menin interacting proteins as clues toward the understanding of multiple endocrine neoplasia type 1

Distinct MDM2 and P14ARF expression and centrosome amplification in well-differentiated liposarcomas

BEK and FLG, two receptors to members of the FGF family, are amplified in subsets of human breast cancers

Three-dimensional culture and differentiation of human osteogenic cells in an injectable hydroxypropylmethylcellulose hydrogel

Proto-oncogene amplification and human breast tumor phenotype

Deregulation of genetic pathways in neuroendocrine tumors

Double minute chromosomes can be produced from precursors derived from a chromosomal deletion

Amplification of FGF-related genes in human tumors: possible involvement of HST in breast carcinomas

Identification of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene

Differential expression of multiple alternative spliceforms of the Men1 tumor suppressor gene in mouse

Mapping genes according to their amplification status in tumor cells : contribution to the map of 11q13

Characterization of the region of the short arm of chromosome 8 amplified in breast carcinoma

The DNA mismatch-repair MLH3 protein interacts with MSH4 in meiotic cells, supporting a role for this MutL homolog in mammalian meiotic recombination

Characterization of the mouse Men1 gene and its expression during development

Characterization of an episome produced in hamster cells that amplify a transfected CAD gene at high frequency: functional evidence for a mammalian replication origin

FCER1B, a candidate gene for atopy, is located in 11q13 between CD20 and TCN1

Germ-Line Mutation Analysis in Patients with Multiple Endocrine Neoplasia Type 1 and Related Disorders

Experimental assessment of the detection limit of genomic amplification by comparative genomic hybridization CGH

Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996

Functional Characterization of a Promoter Region in the Human MEN1 Tumor Suppressor Gene

Novel mutations in the TCIRG1 gene encoding the a3 subunit of the vacuolar proton pump in patients affected by infantile malignant osteopetrosis

The search for the MEN1 gene

Suchergebnisse filtern