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...

LETM1, deleted in Wolf–Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability

Human molecular genetics, 2008-01, Vol.17 (2), p.201-214

2008

Volltextzugriff (PDF)

In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser Syndrome

Molecular syndromology, 2012-04, Vol.2 (6), p.237-244

2012

Volltextzugriff (PDF)

Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1

Journal of medical genetics, 2009-11, Vol.46 (11), p.736-744

2009

Volltextzugriff (PDF)

LETM1, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, flanks the Wolf-Hirschhorn syndrome (WHS) critical region and is deleted in most WHS patients

Genomics (San Diego, Calif.), 1999-09, Vol.60 (2), p.218-225

1999

Volltextzugriff (PDF)

Polymorphisms of Human Estrogen Receptor (ER) Gene Alpha and Beta in Prostate Cancer PC-EW and PC-OR Cell Lines

Anticancer research, 2007-07, Vol.27 (4A), p.2071-2074

2007

Volltextzugriff (PDF)

Partial deletion of 4p and 4q in a fetus with ring chromosome 4: phenotype and molecular mapping of the breakpoints

Journal of medical genetics, 2002-05, Vol.39 (5), p.e23-23

2002

Volltextzugriff (PDF)

Plexiform Hypoglossal Schwannoma in an 11-Year-Old Child: Diagnosis, Management and Review of the Literature

Journal of Surgery and Research, 2020, Vol.3 (4)

2020

Volltextzugriff (PDF)

Assignment of the Human Diacylglycerol Kinase 4 (DAGK4) Gene to Chromosome 4p16.3

Genomics (San Diego, Calif.), 1996-04, Vol.33 (1), p.145-146

1996

Volltextzugriff (PDF)

LETM1, A Novel Gene Encoding a Putative EF-Hand Ca2+-Binding Protein, Flanks the Wolf–Hirschhorn Syndrome (WHS) Critical Region and Is Deleted in Most WHS Patients

Genomics (San Diego, Calif.), 1999-09, Vol.60 (2), p.218-225

1999

Volltextzugriff (PDF)

A novel myosin heavy chain gene in human chromosome 19q13.3

Gene, 2003-07, Vol.312, p.165-171

2003

Volltextzugriff (PDF)

Disruption of ST5 is associated with mental retardation and multiple congenital anomalies

Journal of medical genetics, 2010-02, Vol.47 (2), p.91-98

2010

Volltextzugriff (PDF)

Nicolaides-Baraitser Syndrome

Neuropediatrics, 2013, Vol.44 (2)

2013

Volltextzugriff (PDF)

Human CLAPS2 encoding AP17, a small chain of the clathrin-associated protein complex: cDNA cloning and chromosomal assignment to 19q13.2-->q13.3

Cytogenetic and genome research, 1996-01, Vol.75 (2-3), p.132-135

1996

Volltextzugriff (PDF)

Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS 1

Journal of medical genetics, 2009, Vol.46 (11), p.736-744

2009

Volltextzugriff (PDF)

LETM1, a gene deleted in Wolf–Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein

Genomics (San Diego, Calif.), 2004-02, Vol.83 (2), p.254-261

2004

Volltextzugriff (PDF)

Polymorphisms in the Human Progesterone Receptor (PGR) Gene of Two Human Prostate Adenocarcinoma Cell Lines

Anticancer research, 2005-05, Vol.25 (3A), p.1607-1609

2005

Volltextzugriff (PDF)

Polymorphisms of Human Androgen Receptor (hAR) Gene in Prostate Cancer Cell Lines PC-EW and PC-OR

Anticancer research, 2005-05, Vol.25 (3A), p.1611-1614

2005

Volltextzugriff (PDF)

SPOC1, a novel PHD‐finger protein: Association with residual disease and survival in ovarian cancer

International journal of cancer, 2005-09, Vol.116 (4), p.547-554

2005

Volltextzugriff (PDF)

Identification of novel exons 3' to the human SNRPN gene

Genomics (San Diego, Calif.), 1997-02, Vol.40 (1), p.132-137

1997

Volltextzugriff (PDF)

Assignment of the human diacylglycerol kinase 4 (DAGK4) gene to chromosome 4q16.3

Genomics (San Diego, Calif.), 1996, Vol.33 (1), p.145-146

1996

Volltextzugriff (PDF)

Kirschner-Draht-Osteosynthese von Frakturen des Condylus radialis im Kindes- und Jugendalter

Obere extremität, 2009, Vol.4 (1), p.26-32

2009

Volltextzugriff (PDF)

Quantitative Single-Cell Approaches to Stem Cell Research

Cell stem cell, 2014-11, Vol.15 (5), p.546-558

2014

Volltextzugriff (PDF)

Asymmetric lysosome inheritance predicts activation of haematopoietic stem cells

Nature (London), 2019-09, Vol.573 (7774), p.426-429

2019

Volltextzugriff (PDF)

Prospective identification of hematopoietic lineage choice by deep learning

Nature methods, 2017-04, Vol.14 (4), p.403-406

2017

Volltextzugriff (PDF)

Network plasticity of pluripotency transcription factors in embryonic stem cells

Nature cell biology, 2015-10, Vol.17 (10), p.1235-1246

2015

Volltextzugriff (PDF)

1 – 25 von 100

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(93)
Mit Volltextzugriff
(83)

Publikationsform

Sprache

Englisch
(96)
Deutsch
(4)

Erscheinungsjahr

n.n

Thema

Science & Technology
(69)
Life Sciences & Biomedicine
(60)
Humans
(48)
Male
(38)
Biological And Medical Sciences
(29)
Animals
(27)
Female
(24)
Medical Sciences
(24)
Genetics & Heredity
(23)
Mice
(18)
Adult
(15)
Fundamental And Applied Biological Sciences. Psychology
(13)
Adolescent
(12)
Child, Preschool
(11)
Intellectual Disability - Genetics
(11)
Biotechnology & Applied Microbiology
(10)
Child
(10)
Gene Expression
(10)
Human Genetics
(10)
Molecular Sequence Data
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

LETM1, deleted in Wolf–Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability

In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser Syndrome

Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1

LETM1, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, flanks the Wolf-Hirschhorn syndrome (WHS) critical region and is deleted in most WHS patients

Polymorphisms of Human Estrogen Receptor (ER) Gene Alpha and Beta in Prostate Cancer PC-EW and PC-OR Cell Lines

Partial deletion of 4p and 4q in a fetus with ring chromosome 4: phenotype and molecular mapping of the breakpoints

Plexiform Hypoglossal Schwannoma in an 11-Year-Old Child: Diagnosis, Management and Review of the Literature

Assignment of the Human Diacylglycerol Kinase 4 (DAGK4) Gene to Chromosome 4p16.3

LETM1, A Novel Gene Encoding a Putative EF-Hand Ca2+-Binding Protein, Flanks the Wolf–Hirschhorn Syndrome (WHS) Critical Region and Is Deleted in Most WHS Patients

A novel myosin heavy chain gene in human chromosome 19q13.3

Disruption of ST5 is associated with mental retardation and multiple congenital anomalies

Nicolaides-Baraitser Syndrome

Human CLAPS2 encoding AP17, a small chain of the clathrin-associated protein complex: cDNA cloning and chromosomal assignment to 19q13.2-->q13.3

Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS 1

LETM1, a gene deleted in Wolf–Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein

Polymorphisms in the Human Progesterone Receptor (PGR) Gene of Two Human Prostate Adenocarcinoma Cell Lines

Polymorphisms of Human Androgen Receptor (hAR) Gene in Prostate Cancer Cell Lines PC-EW and PC-OR

SPOC1, a novel PHD‐finger protein: Association with residual disease and survival in ovarian cancer

Identification of novel exons 3' to the human SNRPN gene

Assignment of the human diacylglycerol kinase 4 (DAGK4) gene to chromosome 4q16.3

Kirschner-Draht-Osteosynthese von Frakturen des Condylus radialis im Kindes- und Jugendalter

Quantitative Single-Cell Approaches to Stem Cell Research

Asymmetric lysosome inheritance predicts activation of haematopoietic stem cells

Prospective identification of hematopoietic lineage choice by deep learning

Network plasticity of pluripotency transcription factors in embryonic stem cells

Suchergebnisse filtern