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...

Genetic variation in folate metabolism is associated with the risk of conotruncal heart defects in a Chinese population

BMC pediatrics, 2018-08, Vol.18 (1), p.287-287, Article 287

2018

Volltextzugriff (PDF)

The intervention dilemma and high burden of children with autism in Guizhou province, Southwest China

Frontiers in psychiatry, 2022-11, Vol.13, p.929833-929833

2022

Volltextzugriff (PDF)

Further delineation of autosomal recessive intellectual disability syndrome caused by homozygous variant of the NSUN2 gene in a chinese pedigree

Molecular genetics & genomic medicine, 2020-12, Vol.8 (12), p.e1518-n/a

2020

Volltextzugriff (PDF)

A de novo Variant of ASXL1 Is Associated With an Atypical Phenotype of Bohring-Opitz Syndrome: Case Report and Literature Review

Frontiers in pediatrics, 2021-08, Vol.9

2021

Volltextzugriff (PDF)

Ambient Air Pollution and Daily Hospital Admissions for Respiratory Disease in Children in Guiyang, China

Frontiers in pediatrics, 2019-10, Vol.7, p.400-400

2019

Volltextzugriff (PDF)

A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects

PloS one, 2013-08, Vol.8 (8), p.e72515

2013

Volltextzugriff (PDF)

Exome Sequencing Identifies a Novel MYH7 p.G407C Mutation Responsible for Familial Hypertrophic Cardiomyopathy

DNA and cell biology, 2014-10, Vol.33 (10), p.699-704

2014

Volltextzugriff (PDF)

Magnetic properties of FePc sheet modified by the adsorption of gas molecules

Computational and theoretical chemistry, 2022-08, Vol.1214, p.113793, Article 113793

2022

Volltextzugriff (PDF)

A 55-Day-Old Female Infant Infected With 2019 Novel Coronavirus Disease: Presenting With Pneumonia, Liver Injury, and Heart Damage

The Journal of infectious diseases, 2020-05, Vol.221 (11), p.1775-1781

2020

Volltextzugriff (PDF)

Novel TRAPPC11 Mutations in a Chinese Pedigree of Limb Girdle Muscular Dystrophy

Case reports in genetics, 2018, Vol.2018 (2018), p.1-6

2018

Volltextzugriff (PDF)

Familial congenital heart disease: data collection and preliminary analysis

Cardiology in the young, 2013-06, Vol.23 (3), p.394-399

2013

Volltextzugriff (PDF)

Homozygosity for a novel missense variant of RPGRIP1L causing Joubert syndrome with renal defects in a family of Chinese descent

Clinical nephrology, 2021-10, Vol.96 (4), p.243-250

2021

Volltextzugriff (PDF)

Novel joint catalytic properties of Fe and N co-doped graphene for CO oxidation

Physical chemistry chemical physics : PCCP, 2020-12, Vol.22 (48), p.28376-28382

2020

Volltextzugriff (PDF)

Internal friction peak and damping mechanism in high damping 6061Al/SiCp/Gr hybrid metal matrix composite

Journal of alloys and compounds, 2004-06, Vol.372 (1-2), p.304-308

2004

Volltextzugriff (PDF)

Therapeutic inhibition of CXC chemokine receptor 2 by SB225002 attenuates LPS-induced acute lung injury in mice

Archives of medical science, 2018-04, Vol.14 (3), p.635-644

2018

Volltextzugriff (PDF)

Thymidylate synthase gene variation is associated with the risk for conotruncal heart defects in Chinese population

Cardiology in the young, 2019-03, Vol.29 (3), p.280-285

2019

Volltextzugriff (PDF)

Rh-CXCL-12 Attenuates Neuronal Pyroptosis after Subarachnoid Hemorrhage in Rats via Regulating the CXCR4/NLRP1 Pathway

Oxidative medicine and cellular longevity, 2021, Vol.2021 (1), p.6966394-6966394

2021

Volltextzugriff (PDF)

Corrigendum to: A 55-Day-Old Female Infant Infected With 2019 Novel Coronavirus Disease: Presenting With Pneumonia, Liver Injury, and Heart Damage

The Journal of infectious diseases, 2020-07, Vol.222 (3), p.519-519

2020

Volltextzugriff (PDF)

Identification of two CUL7 variants in two Chinese families with 3‐M syndrome by whole‐exome sequencing

Journal of clinical laboratory analysis, 2020-07, Vol.34 (7), p.e23265-n/a

2020

Volltextzugriff (PDF)

AT1R/GSK-3β/mTOR Signaling Pathway Involved in Angiotensin II-Induced Neuronal Apoptosis after HIE Both In Vitro and In Vivo

Oxidative medicine and cellular longevity, 2020, Vol.2020 (2020), p.1-14

2020

Volltextzugriff (PDF)

Identification of Two Novel Mutations in Patients With X-Linked Primary Immunodeficiencies

Fetal and pediatric pathology, 2015-04, Vol.34 (2), p.91-98

2015

Volltextzugriff (PDF)

Influence of genes and the environment in familial congenital heart defects

Molecular medicine reports, 2014-02, Vol.9 (2), p.695-700

2014

Volltextzugriff (PDF)

Exome sequencing identifies a novel MYH7 p.G407C mutation responsible for familial hypertrophic cardiomyopathy

DNA and cell biology, 2014-10, Vol.33 (10), p.699

2014

Volltextzugriff (PDF)

Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects

Molecular medicine reports, 2014-08, Vol.10 (2), p.743-748

2014

Volltextzugriff (PDF)

Potential role of CRELD1 gene in the pathogenesis of atrioventricular septal defect

Zhonghua yi xue yi chuan xue za zhi, 2014-06, Vol.31 (3), p.263

2014

Volltextzugriff (PDF)

1 – 25 von 308

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(252)
Mit Volltextzugriff
(287)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(211)
Physical Sciences
(101)
Life Sciences & Biomedicine
(83)
Technology
(82)
Chemistry
(81)
Materials Science
(38)
Chemistry, Multidisciplinary
(36)
Materials Science, Multidisciplinary
(34)
Engineering
(31)
Science & Technology - Other Topics
(28)
Physics
(25)
Humans
(23)
Physics, Applied
(22)
Animals
(21)
Chemistry, Physical
(21)
Environmental Sciences & Ecology
(20)
Nanoscience & Nanotechnology
(20)
Environmental Sciences
(19)
Engineering, Environmental
(17)
Computer Science
(16)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(3)
... seit 90 Tagen
(7)

Menü

Weitere Dienste

Einstellungen

Genetic variation in folate metabolism is associated with the risk of conotruncal heart defects in a Chinese population

The intervention dilemma and high burden of children with autism in Guizhou province, Southwest China

Further delineation of autosomal recessive intellectual disability syndrome caused by homozygous variant of the NSUN2 gene in a chinese pedigree

A de novo Variant of ASXL1 Is Associated With an Atypical Phenotype of Bohring-Opitz Syndrome: Case Report and Literature Review

Ambient Air Pollution and Daily Hospital Admissions for Respiratory Disease in Children in Guiyang, China

A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects

Exome Sequencing Identifies a Novel MYH7 p.G407C Mutation Responsible for Familial Hypertrophic Cardiomyopathy

Magnetic properties of FePc sheet modified by the adsorption of gas molecules

A 55-Day-Old Female Infant Infected With 2019 Novel Coronavirus Disease: Presenting With Pneumonia, Liver Injury, and Heart Damage

Novel TRAPPC11 Mutations in a Chinese Pedigree of Limb Girdle Muscular Dystrophy

Familial congenital heart disease: data collection and preliminary analysis

Homozygosity for a novel missense variant of RPGRIP1L causing Joubert syndrome with renal defects in a family of Chinese descent

Novel joint catalytic properties of Fe and N co-doped graphene for CO oxidation

Internal friction peak and damping mechanism in high damping 6061Al/SiCp/Gr hybrid metal matrix composite

Therapeutic inhibition of CXC chemokine receptor 2 by SB225002 attenuates LPS-induced acute lung injury in mice

Thymidylate synthase gene variation is associated with the risk for conotruncal heart defects in Chinese population

Rh-CXCL-12 Attenuates Neuronal Pyroptosis after Subarachnoid Hemorrhage in Rats via Regulating the CXCR4/NLRP1 Pathway

Corrigendum to: A 55-Day-Old Female Infant Infected With 2019 Novel Coronavirus Disease: Presenting With Pneumonia, Liver Injury, and Heart Damage

Identification of two CUL7 variants in two Chinese families with 3‐M syndrome by whole‐exome sequencing

AT1R/GSK-3β/mTOR Signaling Pathway Involved in Angiotensin II-Induced Neuronal Apoptosis after HIE Both In Vitro and In Vivo

Identification of Two Novel Mutations in Patients With X-Linked Primary Immunodeficiencies

Influence of genes and the environment in familial congenital heart defects

Exome sequencing identifies a novel MYH7 p.G407C mutation responsible for familial hypertrophic cardiomyopathy

Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects

Potential role of CRELD1 gene in the pathogenesis of atrioventricular septal defect

Suchergebnisse filtern