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...

Three New Allelic Mouse Mutations that Cause Skeletal Overgrowth Involve the Natriuretic Peptide Receptor C Gene (Npr3)

Proceedings of the National Academy of Sciences - PNAS, 1999-08, Vol.96 (18), p.10278-10283

1999

Volltextzugriff (PDF)

Mouse chromosome 19

Mammalian genome, 1999-10, Vol.10 (10), p.960-960

1999

Volltextzugriff (PDF)

Male sterility caused by sperm cell-specific structural abnormalities in ébouriffé, a new mutation of the house mouse

Biology of reproduction, 1996-08, Vol.55 (2), p.355-363

1996

Volltextzugriff (PDF)

Minisatellite Linkage Maps in the Mouse by Cross-Hybridization with Human Probes Containing Tandem Repeats

Proceedings of the National Academy of Sciences - PNAS, 1990-06, Vol.87 (12), p.4585-4589

1990

Volltextzugriff (PDF)

Regulated expression and RNA processing of transcripts from the Srp20 splicing factor gene during the cell cycle

Molecular and Cellular Biology, 1997-06, Vol.17 (6), p.3116-3124

1997

Volltextzugriff (PDF)

Pathologic changes in the CNS of Dystonia musculorum mutant mouse: An animal model for human spinocerebellar ataxia

Neuroscience, 1988-11, Vol.27 (2), p.403-424

1988

Volltextzugriff (PDF)

Role of H-2 and non-H-2 genes in control of bacterial clearance from the spleen in Salmonella typhimurium-infected mice

Infection and Immunity, 1988-09, Vol.56 (9), p.2407-2411

1988

Volltextzugriff (PDF)

Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7

The EMBO journal, 1986-11, Vol.5 (11), p.2899-2905

1986

Volltextzugriff (PDF)

Comparative mapping of two adjacent regions of MMU19 with their human counterpart on HSA11q13

Cytogenetic and genome research, 1998-01, Vol.81 (3-4), p.237-246

1998

Volltextzugriff (PDF)

hph-1: A Mouse Mutant With Hereditary Hyperphenylalaninemia Induced by Ethylnitrosourea Mutagenesis

Genetics (Austin), 1988-02, Vol.118 (2), p.299-305

1988

Volltextzugriff (PDF)

Pax8, a murine paired box gene expressed in the developing excretory system and thyroid gland

Development (Cambridge), 1990-10, Vol.110 (2), p.643-651

1990

Volltextzugriff (PDF)

Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus

Human genetics, 1990-08, Vol.85 (3), p.324-326

1990

Volltextzugriff (PDF)

The frissonnant Mutant Mouse, a Model of Dopamino-Sensitive, Inherited Motor Syndrome

Neurobiology of disease, 2001-06, Vol.8 (3), p.447-458

2001

Volltextzugriff (PDF)

Erythropoietic protoporphyria in the house mouse : a recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease

The Journal of clinical investigation, 1991-11, Vol.88 (5), p.1730-1736

1991

Volltextzugriff (PDF)

Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus

Journal of investigative dermatology, 1997-09, Vol.109 (3), p.324-328

1997

Volltextzugriff (PDF)

Cardiac and skeletal muscle troponin I isoforms are encoded by a dispersed gene family on mouse chromosomes 1 and 7

Mammalian genome, 1996-01, Vol.7 (1), p.13-15

1996

Volltextzugriff (PDF)

The CD4 T cell-deficient mouse mutation nackt (nkt) involves a deletion in the cathepsin L (CtsI) gene

Immunogenetics (New York), 2001-04, Vol.53 (3), p.233-242

2001

Volltextzugriff (PDF)

Rbt (Rabo torcido), a new mouse skeletal mutation involved in anteroposterior patterning of the axial skeleton, maps close to the Ts (tail-short) locus and distal to the Sox9 locus on chromosome 11

Mammalian genome, 1996-12, Vol.7 (12), p.881-885

1996

Volltextzugriff (PDF)

The Sycp1 loci of the mouse genome : Successive retropositions of a meiotic gene during the recent evolution of the genus

Genomics (San Diego, Calif.), 1997-08, Vol.44 (1), p.118-126

1997

Volltextzugriff (PDF)

Chromosomal assignments of mammalian genes with an acute inflammation-regulated expression in liver

Immunogenetics (New York), 2001-10, Vol.53 (8), p.634-642

2001

Volltextzugriff (PDF)

Genomic organization, chromosomal assignment, and expression analysis of the mouse Suppressor of fused gene (Sufu) coding a Gli protein partner

Mammalian genome, 2000-08, Vol.11 (8), p.614-621

2000

Volltextzugriff (PDF)

Tissue- and Developmental Stage-Specific Imprinting of the Mouse Proinsulin Gene, Ins2

Developmental biology, 1995-04, Vol.168 (2), p.686-688

1995

Volltextzugriff (PDF)

Comparative assignments of the genes of the inter-α-inhibitor family in human and mouse : ITIH4 is close to ITIH1 and ITIH3, on HSA 3 and MMU 14

Genomics (San Diego, Calif.), 1997-04, Vol.41 (1), p.139-140

1997

Volltextzugriff (PDF)

Chromosomal Localization of Muscle Nicotinic Acetylcholine Receptor Genes in the Mouse

Science (American Association for the Advancement of Science), 1986-11, Vol.234 (4778), p.866-868

1986

Volltextzugriff (PDF)

Fim-1, Fim-2/c-fms, and Fim-3, three common integration sites of Friend murine leukemia virus in myeloblastic leukemias, map to mouse chromosomes 13, 18, and 3, respectively

Journal of Virology, 1988-11, Vol.62 (11), p.3973-3978

1988

Volltextzugriff (PDF)

26 – 50 von 426

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(361)
Mit Volltextzugriff
(359)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Animals
(266)
Science & Technology
(245)
Life Sciences & Biomedicine
(222)
Mice
(202)
Chromosome Mapping
(120)
Biological And Medical Sciences
(108)
Genetics & Heredity
(104)
Fundamental And Applied Biological Sciences. Psychology
(88)
Male
(87)
Female
(83)
Humans
(73)
Biochemistry & Molecular Biology
(72)
Molecular Sequence Data
(69)
Base Sequence
(66)
Biotechnology & Applied Microbiology
(61)
Crosses, Genetic
(58)
Mice, Inbred C57bl
(55)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(44)
Mutation
(44)
Genes
(43)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Three New Allelic Mouse Mutations that Cause Skeletal Overgrowth Involve the Natriuretic Peptide Receptor C Gene (Npr3)

Mouse chromosome 19

Male sterility caused by sperm cell-specific structural abnormalities in ébouriffé, a new mutation of the house mouse

Minisatellite Linkage Maps in the Mouse by Cross-Hybridization with Human Probes Containing Tandem Repeats

Regulated expression and RNA processing of transcripts from the Srp20 splicing factor gene during the cell cycle

Pathologic changes in the CNS of Dystonia musculorum mutant mouse: An animal model for human spinocerebellar ataxia

Role of H-2 and non-H-2 genes in control of bacterial clearance from the spleen in Salmonella typhimurium-infected mice

Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7

Comparative mapping of two adjacent regions of MMU19 with their human counterpart on HSA11q13

hph-1: A Mouse Mutant With Hereditary Hyperphenylalaninemia Induced by Ethylnitrosourea Mutagenesis

Pax8, a murine paired box gene expressed in the developing excretory system and thyroid gland

Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus

The frissonnant Mutant Mouse, a Model of Dopamino-Sensitive, Inherited Motor Syndrome

Erythropoietic protoporphyria in the house mouse : a recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease

Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus

Cardiac and skeletal muscle troponin I isoforms are encoded by a dispersed gene family on mouse chromosomes 1 and 7

The CD4 T cell-deficient mouse mutation nackt (nkt) involves a deletion in the cathepsin L (CtsI) gene

Rbt (Rabo torcido), a new mouse skeletal mutation involved in anteroposterior patterning of the axial skeleton, maps close to the Ts (tail-short) locus and distal to the Sox9 locus on chromosome 11

The Sycp1 loci of the mouse genome : Successive retropositions of a meiotic gene during the recent evolution of the genus

Chromosomal assignments of mammalian genes with an acute inflammation-regulated expression in liver

Genomic organization, chromosomal assignment, and expression analysis of the mouse Suppressor of fused gene (Sufu) coding a Gli protein partner

Tissue- and Developmental Stage-Specific Imprinting of the Mouse Proinsulin Gene, Ins2

Comparative assignments of the genes of the inter-α-inhibitor family in human and mouse : ITIH4 is close to ITIH1 and ITIH3, on HSA 3 and MMU 14

Chromosomal Localization of Muscle Nicotinic Acetylcholine Receptor Genes in the Mouse

Fim-1, Fim-2/c-fms, and Fim-3, three common integration sites of Friend murine leukemia virus in myeloblastic leukemias, map to mouse chromosomes 13, 18, and 3, respectively

Suchergebnisse filtern