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...

A clinical and molecular genetic study of 112 Iranian families with primary microcephaly

Journal of medical genetics, 2010-12, Vol.47 (12), p.823-828

2010

Volltextzugriff (PDF)

Polymorphic AP-1 Binding Site in Bovine CSN1S1 Shows Quantitative Differences in Protein Binding Associated with Milk Protein Expression

Journal of dairy science, 2005-06, Vol.88 (6), p.2246-2252

2005

Volltextzugriff (PDF)

Associations of a Polymorphic AP-2 Binding Site in the 5′-Flanking Region of the Bovine β-Lactoglobulin Gene with Milk Proteins

Journal of dairy science, 2003-06, Vol.86 (6), p.2213-2218

2003

Volltextzugriff (PDF)

Generation of two isogenic iPSC lines from a healthy male donor of European ancestry

Stem cell research, 2024-06, Vol.77, p.103403, Article 103403

2024

Volltextzugriff (PDF)

Generation of two iPSC lines (MHHi001-A-12 and MHHi001-A-13) carrying biallelic truncating mutations at the 3'-end of SRCAP using CRISPR/Cas9

Stem cell research, 2023-12, Vol.73, p.103249-103249, Article 103249

2023

Volltextzugriff (PDF)

Comparison of Vietnamese and European pig breeds using microsatellites

Journal of animal science, 2006-10, Vol.84 (10), p.2601

2006

Volltextzugriff (PDF)

Generation of an iPSC line (UMGWi001-B) from a patient with Floating-Harbor Syndrome (FLHS) carrying a heterozygous SRCAP mutation (p.Arg2444)

Stem cell research, 2020-12, Vol.49, p.102028-102028, Article 102028

2020

Volltextzugriff (PDF)

Alopecia-mental retardation syndrome: clinical and molecular characterization of four patients

British journal of dermatology (1951), 2008-09, Vol.159 (3), p.748-751

2008

Volltextzugriff (PDF)

Methylation and Expression Analyses of the 7q Autism Susceptibility Locus Genes MEST, COPG2, and TSGA14 in Human and Anthropoid Primate Cortices

Cytogenetic and genome research, 2012-06, Vol.136 (4), p.278-287

2012

Volltextzugriff (PDF)

Comparison of Vietnamese and European pig breeds using microsatellites1

Journal of animal science, 2006-10, Vol.84 (10), p.2601-2608

2006

Volltextzugriff (PDF)

A High Density of Human Communication-Associated Genes in Chromosome 7q31-q36: Differential Expression in Human and Non-Human Primate Cortices

Cytogenetic and genome research, 2012-01, Vol.136 (2), p.97-106

2012

Volltextzugriff (PDF)

Nine porcine microsatellite loci tested for size homoplasy in genetically diverse breeds

Animal genetics, 2005-06, Vol.36 (3), p.244-247

2005

Volltextzugriff (PDF)

Analysis of polymorphic PRNP microsatellite and ORF sites in German sheep breeds

Journal of animal breeding and genetics (1986), 2005-04, Vol.122 (s1), p.64-70

2005

Volltextzugriff (PDF)

Mitochondria-Dependent Caspase-9 Activation Is Necessary for Antigen Receptor-Mediated Effector Caspase Activation and Apoptosis in WEHI 231 Lymphoma Cells

The Journal of immunology (1950), 2002-04, Vol.168 (8), p.3902-3909

2002

Volltextzugriff (PDF)

Associations of a Polymorphic AP-2 Binding Site in the 5'-Flanking Region of the Bovine {beta}-Lactoglobulin Gene with Milk Proteins

Journal of dairy science, 2003-06, Vol.86 (6), p.2213

2003

Volltextzugriff (PDF)

Blimp‐1 over‐expression abrogates IL‐4‐ and CD40‐mediated suppression of terminal B cell differentiation but arrests isotype switching

European journal of immunology, 2001-07, Vol.31 (7), p.1972-1980

2001

Volltextzugriff (PDF)

A1 expression is stimulated by CD40 in B cells and rescues WEHI 231 cells from anti‐IgM‐induced cell death

European journal of immunology, 1999-10, Vol.29 (10), p.3077-3088

1999

Volltextzugriff (PDF)

A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation

American journal of human genetics, 2008-05, Vol.82 (5), p.1158-1164

2008

Volltextzugriff (PDF)

Subgroup-elimination transcriptomics identifies signaling proteins that define subclasses of TRPV1-positive neurons and a novel paracrine circuit

PloS one, 2014-12, Vol.9 (12), p.e115731-e115731

2014

Volltextzugriff (PDF)

Reversal of Blimp‐1‐mediated apoptosis by A1, a member of the Bcl‐2 family

European journal of immunology, 1999-09, Vol.29 (9), p.2988-2998

1999

Volltextzugriff (PDF)

BDNF: mRNA expression in urine cells of patients with chronic kidney disease and its role in kidney function

Journal of cellular and molecular medicine, 2018-11, Vol.22 (11), p.5265-5277

2018

Volltextzugriff (PDF)

Das methodische Potenzial der neuen Sequenziertechnologien jenseits der Mutationssuche

Medizinische Genetik, 2014, Vol.26 (2), p.264-272

Kuss, A.W.

2014

Volltextzugriff (PDF)

OLA-DRB1 microsatellite variants are associated with ovine growth and reproduction traits

Genetics selection evolution (Paris), 2006-08, Vol.38 (4), p.431-444

2006

Volltextzugriff (PDF)

SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

Human genetics, 2006-02, Vol.118 (6), p.708-715

2006

Volltextzugriff (PDF)

1 – 25 von 648

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(575)
Mit Volltextzugriff
(603)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(401)
Physics
(235)
Physical Sciences
(212)
Astronomy And Astrophysics
(173)
Astrophysics
(173)
Life Sciences & Biomedicine
(166)
Astronomy & Astrophysics
(160)
Sciences Of The Universe
(125)
Humans
(121)
High Energy Astrophysical Phenomena
(106)
Fysik
(93)
Male
(85)
Female
(84)
Natural Sciences
(84)
Naturvetenskap
(84)
Exact Sciences And Technology
(73)
Astronomy
(71)
Earth, Ocean, Space
(66)
Astronomi Och Astrofysik
(64)
Adult
(59)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

A clinical and molecular genetic study of 112 Iranian families with primary microcephaly

X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome

Polymorphic AP-1 Binding Site in Bovine CSN1S1 Shows Quantitative Differences in Protein Binding Associated with Milk Protein Expression

Associations of a Polymorphic AP-2 Binding Site in the 5′-Flanking Region of the Bovine β-Lactoglobulin Gene with Milk Proteins

Generation of two isogenic iPSC lines from a healthy male donor of European ancestry

Generation of two iPSC lines (MHHi001-A-12 and MHHi001-A-13) carrying biallelic truncating mutations at the 3'-end of SRCAP using CRISPR/Cas9

Comparison of Vietnamese and European pig breeds using microsatellites

Generation of an iPSC line (UMGWi001-B) from a patient with Floating-Harbor Syndrome (FLHS) carrying a heterozygous SRCAP mutation (p.Arg2444)

Alopecia-mental retardation syndrome: clinical and molecular characterization of four patients

Methylation and Expression Analyses of the 7q Autism Susceptibility Locus Genes MEST, COPG2, and TSGA14 in Human and Anthropoid Primate Cortices

Comparison of Vietnamese and European pig breeds using microsatellites1

A High Density of Human Communication-Associated Genes in Chromosome 7q31-q36: Differential Expression in Human and Non-Human Primate Cortices

Nine porcine microsatellite loci tested for size homoplasy in genetically diverse breeds

Analysis of polymorphic PRNP microsatellite and ORF sites in German sheep breeds

Mitochondria-Dependent Caspase-9 Activation Is Necessary for Antigen Receptor-Mediated Effector Caspase Activation and Apoptosis in WEHI 231 Lymphoma Cells

Associations of a Polymorphic AP-2 Binding Site in the 5'-Flanking Region of the Bovine {beta}-Lactoglobulin Gene with Milk Proteins

Blimp‐1 over‐expression abrogates IL‐4‐ and CD40‐mediated suppression of terminal B cell differentiation but arrests isotype switching

A1 expression is stimulated by CD40 in B cells and rescues WEHI 231 cells from anti‐IgM‐induced cell death

A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation

Subgroup-elimination transcriptomics identifies signaling proteins that define subclasses of TRPV1-positive neurons and a novel paracrine circuit

Reversal of Blimp‐1‐mediated apoptosis by A1, a member of the Bcl‐2 family

BDNF: mRNA expression in urine cells of patients with chronic kidney disease and its role in kidney function

Das methodische Potenzial der neuen Sequenziertechnologien jenseits der Mutationssuche

OLA-DRB1 microsatellite variants are associated with ovine growth and reproduction traits

SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

Suchergebnisse filtern