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...

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

The Lancet (British edition), 2012-11, Vol.380 (9854), p.1674-1682

2012

Volltextzugriff (PDF)

Derivation and expansion using only small molecules of human neural progenitors for neurodegenerative disease modeling

PloS one, 2013-03, Vol.8 (3), p.e59252-e59252

2013

Volltextzugriff (PDF)

Extrinsic immune cell-derived, but not intrinsic oligodendroglial factors contribute to oligodendroglial differentiation block in multiple sclerosis

Acta neuropathologica, 2020-11, Vol.140 (5), p.715-736

2020

Volltextzugriff (PDF)

Cardiogenic programming of human pluripotent stem cells by dose-controlled activation of EOMES

Nature communications, 2018-01, Vol.9 (1), p.440-8, Article 440

2018

Volltextzugriff (PDF)

Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome

PloS one, 2011-04, Vol.6 (4), p.e19426

2011

Volltextzugriff (PDF)

Astrocyte pathology in a human neural stem cell model of frontotemporal dementia caused by mutant TAU protein

Scientific reports, 2017-03, Vol.7 (1), p.42991-42991, Article 42991

2017

Volltextzugriff (PDF)

Initial experience with [18F]DPA-714 TSPO-PET to image inflammation in primary angiitis of the central nervous system

European journal of nuclear medicine and molecular imaging, 2020-08, Vol.47 (9), p.2131-2141

2020

Volltextzugriff (PDF)

X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men

The New England journal of medicine, 2015-05, Vol.372 (22), p.2097-2107

2015

Volltextzugriff (PDF)

Action of steroids and plant triterpenoids on CatSper Ca2+ channels in human sperm

Proceedings of the National Academy of Sciences - PNAS, 2018-01, Vol.115 (3), p.E344-E346

2018

Volltextzugriff (PDF)

The first versatile human iPSC-based model of ectopic virus induction allows new insights in RNA-virus disease

Scientific reports, 2020-10, Vol.10 (1), p.16804, Article 16804

2020

Volltextzugriff (PDF)

Cardiac Subtype-Specific Modeling of Kv1.5 Ion Channel Deficiency Using Human Pluripotent Stem Cells

Frontiers in physiology, 2017-07, Vol.8, p.469-469

2017

Volltextzugriff (PDF)

Generation of a human iPSC line (MPIi008-A) from a patient with Denys-Drash syndrome

Stem cell research, 2022-07, Vol.62, p.102826-102826, Article 102826

2022

Volltextzugriff (PDF)

Generation of a human iPSC line (MPIi006-A) from a patient with Pelizaeus-Merzbacher disease

Stem cell research, 2020-07, Vol.46, p.101839-101839, Article 101839

2020

Volltextzugriff (PDF)

Generation and cardiac subtype-specific differentiation of PITX2-deficient human iPS cell lines for exploring familial atrial fibrillation

Stem cell research, 2017-05, Vol.21 (C), p.26-28

2017

Volltextzugriff (PDF)

Severe, very early onset preeclampsia in a Covid 19-positive woman with a twin pregnancy presenting with a hydatidiform mole and coexisting normal fetus: a case report

Frontiers in medicine, 2024-02, Vol.11, p.1340905

2024

Volltextzugriff (PDF)

Distinct Neurodegenerative Changes in an Induced Pluripotent Stem Cell Model of Frontotemporal Dementia Linked to Mutant TAU Protein

Stem cell reports, 2015-07, Vol.5 (1), p.83-96

2015

Volltextzugriff (PDF)

Generation of a human iPSC line (MPIi007-A) from a patient with Metachromatic leukodystrophy

Stem cell research, 2020-10, Vol.48, p.101993, Article 101993

2020

Volltextzugriff (PDF)

Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line

Stem cell research, 2020-07, Vol.46, p.101855-101855, Article 101855

2020

Volltextzugriff (PDF)

Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual

Stem cell research, 2020-07, Vol.46, p.101820-101820, Article 101820

2020

Volltextzugriff (PDF)

Disorders of spermatogenesis

Medizinische Genetik, 2018-03, Vol.30 (1), p.12-20

2018

Volltextzugriff (PDF)

Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine

Medizinische Genetik, 2018, Vol.30 (1), p.12-20

2018

Volltextzugriff (PDF)

Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males

European journal of human genetics : EJHG, 2013-09, Vol.21 (9), p.1012-1015

2013

Volltextzugriff (PDF)

Universal Cardiac Induction of Human Pluripotent Stem Cells in Two and Three‐Dimensional Formats: Implications for In Vitro Maturation

Stem cells (Dayton, Ohio), 2015-05, Vol.33 (5), p.1456-1469

2015

Volltextzugriff (PDF)

MECHANISMS IN ENDOCRINOLOGY: Aberrations of the X chromosome as cause of male infertility

European journal of endocrinology, 2017-11, Vol.177 (5), p.R249-R259

2017

Volltextzugriff (PDF)

Characterization of endometrial mesenchymal stem-like cells obtained by endometrial biopsy during routine diagnostics

Fertility and sterility, 2011, Vol.95 (1), p.423-426

2011

Volltextzugriff (PDF)

1 – 25 von 78

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(70)
Mit Volltextzugriff
(73)

Publikationsform

Sprache

Englisch
(76)
Deutsch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

Derivation and expansion using only small molecules of human neural progenitors for neurodegenerative disease modeling

Extrinsic immune cell-derived, but not intrinsic oligodendroglial factors contribute to oligodendroglial differentiation block in multiple sclerosis

Cardiogenic programming of human pluripotent stem cells by dose-controlled activation of EOMES

Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome

Astrocyte pathology in a human neural stem cell model of frontotemporal dementia caused by mutant TAU protein

Initial experience with [18F]DPA-714 TSPO-PET to image inflammation in primary angiitis of the central nervous system

X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men

Action of steroids and plant triterpenoids on CatSper Ca2+ channels in human sperm

The first versatile human iPSC-based model of ectopic virus induction allows new insights in RNA-virus disease

Cardiac Subtype-Specific Modeling of Kv1.5 Ion Channel Deficiency Using Human Pluripotent Stem Cells

Generation of a human iPSC line (MPIi008-A) from a patient with Denys-Drash syndrome

Generation of a human iPSC line (MPIi006-A) from a patient with Pelizaeus-Merzbacher disease

Generation and cardiac subtype-specific differentiation of PITX2-deficient human iPS cell lines for exploring familial atrial fibrillation

Severe, very early onset preeclampsia in a Covid 19-positive woman with a twin pregnancy presenting with a hydatidiform mole and coexisting normal fetus: a case report

Distinct Neurodegenerative Changes in an Induced Pluripotent Stem Cell Model of Frontotemporal Dementia Linked to Mutant TAU Protein

Generation of a human iPSC line (MPIi007-A) from a patient with Metachromatic leukodystrophy

Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line

Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual

Disorders of spermatogenesis

Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine

Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males

Universal Cardiac Induction of Human Pluripotent Stem Cells in Two and Three‐Dimensional Formats: Implications for In Vitro Maturation

MECHANISMS IN ENDOCRINOLOGY: Aberrations of the X chromosome as cause of male infertility

Characterization of endometrial mesenchymal stem-like cells obtained by endometrial biopsy during routine diagnostics

Suchergebnisse filtern