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...

Phenotypic variability in LAMA3‐associated amelogenesis imperfecta

Oral diseases, 2023-11, Vol.29 (8), p.3514-3524

2023

Volltextzugriff (PDF)

FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome

International endodontic journal, 2023-08, Vol.56 (8), p.943-954

2023

Volltextzugriff (PDF)

PAX9 mutations and genetic synergism in familial tooth agenesis

Annals of the New York Academy of Sciences, 2023-06, Vol.1524 (1), p.87-96

2023

Volltextzugriff (PDF)

Mouse Dspp frameshift model of human dentinogenesis imperfecta

Scientific reports, 2021-10, Vol.11 (1), p.20653-20653, Article 20653

2021

Volltextzugriff (PDF)

Transcriptome analysis of gingival tissues of enamel‐renal syndrome

Journal of periodontal research, 2019-12, Vol.54 (6), p.653-661

2019

Volltextzugriff (PDF)

AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta

International journal of molecular sciences, 2024-06, Vol.25 (11), p.6132

2024

Volltextzugriff (PDF)

Craniofacial and olfactory sensory changes after long-term unilateral nasal obstruction—an animal study using MMP-3-LUC transgenic rats

Scientific reports, 2024-01, Vol.14 (1), p.2616-9, Article 2616

2024

Volltextzugriff (PDF)

Photocatalytic activities of Pd-loaded mesoporous TiO2 thin films

Chemical engineering journal (Lausanne, Switzerland : 1996), 2009-10, Vol.152 (2-3), p.492-497

2009

Volltextzugriff (PDF)

Molecular signaling and mechanisms of low-level laser-induced gene expression in cells involved in orthodontic tooth movement

Journal of the Formosan Medical Association, 2024-04, Vol.123 (4), p.442-451

2024

Volltextzugriff (PDF)

Potential contribution of neural crest cells to dental enamel formation

Biochemical and biophysical research communications, 2011-11, Vol.415 (1), p.114-119

2011

Volltextzugriff (PDF)

FAM20A mutations can cause enamel-renal syndrome (ERS)

PLoS genetics, 2013-02, Vol.9 (2), p.e1003302

2013

Volltextzugriff (PDF)

ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta

Human molecular genetics, 2014-04, Vol.23 (8), p.2157-2163

2014

Volltextzugriff (PDF)

Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities

PloS one, 2012-12, Vol.7 (12), p.e51533

2012

Volltextzugriff (PDF)

The implication of integrating pediatric education into a pediatric dentistry course for undergraduate dental students

Journal of dental sciences, 2023-10, Vol.18 (4), p.1794-1803

2023

Volltextzugriff (PDF)

Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds

Molecular genetics & genomic medicine, 2015-01, Vol.3 (1), p.40-58

2015

Volltextzugriff (PDF)

ENAM mutations and digenic inheritance

Molecular genetics & genomic medicine, 2019-10, Vol.7 (10), p.e00928-n/a

2019

Volltextzugriff (PDF)

FAM20C Functions Intracellularly Within Both Ameloblasts and Odontoblasts In Vivo

Journal of bone and mineral research, 2013-12, Vol.28 (12), p.2508-2511

2013

Volltextzugriff (PDF)

Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis

Journal of personalized medicine, 2021-11, Vol.11 (11), p.1217

2021

Volltextzugriff (PDF)

Dental malformations associated with biallelic MMP20 mutations

Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1307-n/a

2020

Volltextzugriff (PDF)

AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout‐NLS‐lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue‐specificity

Molecular genetics & genomic medicine, 2019-09, Vol.7 (9), p.e929-n/a

2019

Volltextzugriff (PDF)

The Modified Shields Classification and 12 Families with Defined DSPP Mutations

Genes, 2022-05, Vol.13 (5), p.858

2022

Volltextzugriff (PDF)

The Enamel Phenotype in Homozygous Fam83h Truncation Mice

Molecular genetics & genomic medicine, 2019-06, Vol.7 (6), p.e724-n/a

2019

Volltextzugriff (PDF)

Critical roles for WDR72 in calcium transport and matrix protein removal during enamel maturation

Molecular genetics & genomic medicine, 2015-07, Vol.3 (4), p.302-319

2015

Volltextzugriff (PDF)

Fam83h null mice support a neomorphic mechanism for human ADHCAI

Molecular genetics & genomic medicine, 2016-01, Vol.4 (1), p.46-67

2016

Volltextzugriff (PDF)

Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC)

Oral surgery, oral medicine, oral pathology and oral radiology, 2015-12, Vol.120 (6), p.e235-e239

2015

Volltextzugriff (PDF)

1 – 25 von 166

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(135)
Mit Volltextzugriff
(146)

Publikationsform

Artikel
(144)
Tagungsberichte
(22)

Sprache

Englisch
(166)

Erscheinungsjahr

n.n

Thema

Science & Technology
(111)
Life Sciences & Biomedicine
(50)
Technology
(45)
Humans
(40)
Physical Sciences
(33)
Engineering
(32)
Male
(27)
Physics
(25)
Engineering, Electrical & Electronic
(23)
Female
(23)
Mutation
(20)
Animals
(17)
Enamel
(17)
Mice
(16)
Physics, Applied
(16)
Dental Enamel
(14)
Exact Sciences And Technology
(14)
Teeth
(14)
Adult
(12)
Middle Aged
(12)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Phenotypic variability in LAMA3‐associated amelogenesis imperfecta

FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome

PAX9 mutations and genetic synergism in familial tooth agenesis

Mouse Dspp frameshift model of human dentinogenesis imperfecta

Transcriptome analysis of gingival tissues of enamel‐renal syndrome

AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta

Craniofacial and olfactory sensory changes after long-term unilateral nasal obstruction—an animal study using MMP-3-LUC transgenic rats

Photocatalytic activities of Pd-loaded mesoporous TiO2 thin films

Molecular signaling and mechanisms of low-level laser-induced gene expression in cells involved in orthodontic tooth movement

Potential contribution of neural crest cells to dental enamel formation

FAM20A mutations can cause enamel-renal syndrome (ERS)

ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta

Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities

The implication of integrating pediatric education into a pediatric dentistry course for undergraduate dental students

Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds

ENAM mutations and digenic inheritance

FAM20C Functions Intracellularly Within Both Ameloblasts and Odontoblasts In Vivo

Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis

Dental malformations associated with biallelic MMP20 mutations

AMBN mutations causing hypoplastic amelogenesis imperfecta and Ambn knockout‐NLS‐lacZ knockin mice exhibiting failed amelogenesis and Ambn tissue‐specificity

The Modified Shields Classification and 12 Families with Defined DSPP Mutations

The Enamel Phenotype in Homozygous Fam83h Truncation Mice

Critical roles for WDR72 in calcium transport and matrix protein removal during enamel maturation

Fam83h null mice support a neomorphic mechanism for human ADHCAI

Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC)

Suchergebnisse filtern