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...

MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency

PloS one, 2018-11, Vol.13 (11), p.e0206184-e0206184

2018

Volltextzugriff (PDF)

Selective Ablation of Tumorigenic Cells Following Human Induced Pluripotent Stem Cell‐Derived Neural Stem/Progenitor Cell Transplantation in Spinal Cord Injury

Stem cells translational medicine, 2019-03, Vol.8 (3), p.260-270

2019

Volltextzugriff (PDF)

A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency

Endocrine Journal, 2017, Vol.64(2), pp.229-234

2017

Volltextzugriff (PDF)

The developmental programme for genesis of the entire kidney is recapitulated in Wilms tumour

PloS one, 2017-10, Vol.12 (10), p.e0186333-e0186333

2017

Volltextzugriff (PDF)

Germline mutations and somatic inactivation of TRIM28 in Wilms tumour

PLoS genetics, 2018-06, Vol.14 (6), p.e1007399

2018

Volltextzugriff (PDF)

The Mosaicism Ratio of 45,X May Explain the Phenotype in a Case of Mixed Gonadal Dysgenesis

Sexual development, 2018-01, Vol.12 (4), p.175-179

2018

Volltextzugriff (PDF)

A novel truncating mutation in MYH3 causes spondylocarpotarsal synostosis syndrome with basilar invagination

Journal of human genetics, 2018-12, Vol.63 (12), p.1277-1281

2018

Volltextzugriff (PDF)

Pathological classification of human iPSC-derived neural stem/progenitor cells towards safety assessment of transplantation therapy for CNS diseases

Molecular brain, 2016-09, Vol.9 (1), p.85, Article 85

2016

Volltextzugriff (PDF)

Destabilized adhesion in the gastric proliferative zone and c-Src kinase activation mark the development of early diffuse gastric cancer

Cancer research (Chicago, Ill.), 2007-03, Vol.67 (6), p.2480-2489

2007

Volltextzugriff (PDF)

Gonadal macrophage infiltration in congenital lipoid adrenal hyperplasia

European journal of endocrinology, 2016-08, Vol.175 (2), p.127-132

2016

Volltextzugriff (PDF)

A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency

ENDOCRINE JOURNAL, 2017-02, Vol.64 (2), p.229-234

2017

Volltextzugriff (PDF)

A novel mutation in LEPRE1 that eliminates only the KDEL ER- retrieval sequence causes non-lethal osteogenesis imperfecta

PloS one, 2012-05, Vol.7 (5), p.e36809-e36809

2012

Volltextzugriff (PDF)

Use of the Naphthoquinone YM155 (Sepantronium Bromide) in the Treatment of Cancer: A Systematic Review and Meta-Synthesis

Oncologie (Paris, France), 2022, Vol.24 (2), p.195-225

2022

Volltextzugriff (PDF)

A report of two novel NR5A1 mutation families: possible clinical phenotype of psychiatric symptoms of anxiety and/or depression

Clinical endocrinology (Oxford), 2013-06, Vol.78 (6), p.957-965

2013

Volltextzugriff (PDF)

Membranoproliferative glomerulonephritis and C3 glomerulonephritis: Frequency, clinical features, and outcome in children

Nephrology (Carlton, Vic.), 2015-04, Vol.20 (4), p.286-292

2015

Volltextzugriff (PDF)

A case of transient neonatal diabetes due to a novel mutation in ABCC8

Clinical Pediatric Endocrinology, 2016, Vol.25(4), pp.139-141

2016

Volltextzugriff (PDF)

Syndromic disorder of sex development due to a novel hemizygous mutation in the carboxyl-terminal domain of ATRX

Human genome variation, 2017-04, Vol.4 (1), p.17012-17012, Article 17012

2017

Volltextzugriff (PDF)

PAX8 Mutation Disturbing Thyroid Follicular Growth: A Case Report

The journal of clinical endocrinology and metabolism, 2011-12, Vol.96 (12), p.E2039-E2044

2011

Volltextzugriff (PDF)

Neonatal necrotizing fasciitis of the scrotum caused by Streptococcus agalactiae

Pediatrics international, 2015-04, Vol.57 (2), p.e56-e58

2015

Volltextzugriff (PDF)

Human Papillomavirus E6 / E7 Expression in Preeclampsia-Affected Placentae

Pathogens (Basel), 2020-03, Vol.9 (3), p.239

2020

Volltextzugriff (PDF)

Characteristic Testicular Histology Is Useful for the Identification of NR5A1 Gene Mutations in Prepubertal 46,XY Patients

Hormone research in paediatrics, 2013-01, Vol.80 (2), p.119-128

2013

Volltextzugriff (PDF)

Laparoscopic subtotal colectomy for a patient with chronic idiopathic colonic pseudo‐obstruction: Report of a case

Asian journal of endoscopic surgery, 2019-10, Vol.12 (4), p.469-472

2019

Volltextzugriff (PDF)

Multifocal Skin Lesions and Melena with Thrombocytopenia in an Infant

The Journal of pediatrics, 2012-03, Vol.160 (3), p.524-524.e1

2012

Volltextzugriff (PDF)

A Novel Case of Somatic KCNJ5 Mutation in Pediatric-Onset Aldosterone-Producing Adenoma

Journal of the Endocrine Society, 2017-08, Vol.1 (8), p.1056-1061

2017

Volltextzugriff (PDF)

Heterozygous C‐propeptide mutations in COL1A1: Osteogenesis imperfecta type IIC and dense bone variant

American journal of medical genetics. Part A, 2011-09, Vol.155 (9), p.2269-2273

2011

Volltextzugriff (PDF)

1 – 25 von 118

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(99)
Mit Volltextzugriff
(108)

Publikationsform

Artikel
(109)
Berichte
(9)

Sprache

Englisch
(110)
Japanisch
(9)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency

Selective Ablation of Tumorigenic Cells Following Human Induced Pluripotent Stem Cell‐Derived Neural Stem/Progenitor Cell Transplantation in Spinal Cord Injury

A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency

The developmental programme for genesis of the entire kidney is recapitulated in Wilms tumour

Germline mutations and somatic inactivation of TRIM28 in Wilms tumour

The Mosaicism Ratio of 45,X May Explain the Phenotype in a Case of Mixed Gonadal Dysgenesis

A novel truncating mutation in MYH3 causes spondylocarpotarsal synostosis syndrome with basilar invagination

Pathological classification of human iPSC-derived neural stem/progenitor cells towards safety assessment of transplantation therapy for CNS diseases

Destabilized adhesion in the gastric proliferative zone and c-Src kinase activation mark the development of early diffuse gastric cancer

Gonadal macrophage infiltration in congenital lipoid adrenal hyperplasia

A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency

A novel mutation in LEPRE1 that eliminates only the KDEL ER- retrieval sequence causes non-lethal osteogenesis imperfecta

Use of the Naphthoquinone YM155 (Sepantronium Bromide) in the Treatment of Cancer: A Systematic Review and Meta-Synthesis

A report of two novel NR5A1 mutation families: possible clinical phenotype of psychiatric symptoms of anxiety and/or depression

Membranoproliferative glomerulonephritis and C3 glomerulonephritis: Frequency, clinical features, and outcome in children

A case of transient neonatal diabetes due to a novel mutation in ABCC8

Syndromic disorder of sex development due to a novel hemizygous mutation in the carboxyl-terminal domain of ATRX

PAX8 Mutation Disturbing Thyroid Follicular Growth: A Case Report

Neonatal necrotizing fasciitis of the scrotum caused by Streptococcus agalactiae

Human Papillomavirus E6 / E7 Expression in Preeclampsia-Affected Placentae

Characteristic Testicular Histology Is Useful for the Identification of NR5A1 Gene Mutations in Prepubertal 46,XY Patients

Laparoscopic subtotal colectomy for a patient with chronic idiopathic colonic pseudo‐obstruction: Report of a case

Multifocal Skin Lesions and Melena with Thrombocytopenia in an Infant

A Novel Case of Somatic KCNJ5 Mutation in Pediatric-Onset Aldosterone-Producing Adenoma

Heterozygous C‐propeptide mutations in COL1A1: Osteogenesis imperfecta type IIC and dense bone variant

Suchergebnisse filtern