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PubPharm (23)
1
Histologic Aspect of the Curved Vomerine Mucosa in Cleft Lip and Palate
enthalten in:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
| 2022
von
Benitez, B.
|
Brudnicki, A.
|
Nalabothu, P.
| +3
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2
Post-mortem magnetic resonance imaging with computed tomography-guided biopsy for foetuses and infants : a prospective, multicentre, cross-sectional study
enthalten in:
BMC pediatrics
| 2022
von
Rüegger, C.
|
Gascho, D.
|
Bode, P.
| +27
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3
Lack of Mucosal Cholinergic Innervation Is Associated With Increased Risk of Enterocolitis in Hirschsprung's Disease
enthalten in:
Cellular and molecular gastroenterology and hepatology
| 2021
von
Keck, S.
|
Galati-Fournier, V.
|
Kym, U.
| +14
CommentIn: Cell Mol Gastroenterol Hepatol. 2021;12(2):785-786. - PMID 34087230
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4
Expanding the spectrum of SMAD3-related phenotypes to agnathia-otocephaly
enthalten in:
Molecular genetics & genomic medicine
| 2020
von
Meier, N.
|
Bruder, E.
|
Miny, P.
| +2
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5
Hectd1 is essential for embryogenesis in mice
enthalten in:
Gene expression patterns : GEP
| 2019
von
D'Alonzo, D.
|
Emch, F.
|
Shen, X.
| +3
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6
Exome sequencing of fetal anomaly syndromes : novel phenotype-genotype discoveries
enthalten in:
European journal of human genetics : EJHG
| 2019
von
Meier, N.
|
Bruder, E.
|
Lapaire, O.
| +10
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7
HECTD1 controls the protein level of IQGAP1 to regulate the dynamics of adhesive structures
enthalten in:
Cell communication and signaling : CCS
| 2017
von
Shen, X.
|
Jia, Z.
|
D'Alonzo, D.
| +5
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8
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF
enthalten in:
Human mutation
| 2016
von
Filges, I.
|
Bruder, E.
|
Brandal, K.
| +16
ErratumIn: Hum Mutat. 2016 Jul;37(7):711. - PMID 27300082
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9
Actinomyces neuii Isolated From a 20-Month-Old Girl With Cervical Lymphadenitis
enthalten in:
Journal of the Pediatric Infectious Diseases Society
| 2015
von
Walther, K.
|
Bruder, E.
|
Goldenberger, D.
| +3
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10
Gene expression profiles of similarly derived human embryonic stem cell lines correlate with their distinct propensity to exit stemness and their different differentiation behavior in culture
enthalten in:
Cellular reprogramming
| 2014
von
Sterthaus, O.
|
Feutz, A.
|
Zhang, H.
| +6
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Thema: Research Support, Non-U.S. Gov't
Medienart
23
Aufsätze
18
E-Artikel
18
E-Ressourcen
5
Gedruckte Aufsätze
Zeitschriftentitel
2
BMC pediatrics
2
Human pathology
1
Acta neuropathologica
1
Cell communication and signaling : CCS
1
Cellular and molecular gastroenterology and hep...
1
Cellular reprogramming
1
European journal of human genetics : EJHG
1
Gene expression patterns : GEP
1
Gut
1
Human mutation
1
Journal of hepatology
1
Journal of the Pediatric Infectious Diseases So...
1
Modern pathology : an official journal of the U...
1
Molecular and cellular biology
1
Molecular genetics & genomic medicine
1
Neoplasia (New York, N.Y.)
1
Neurocritical care
1
Scientific reports
1
The American journal of surgical pathology
1
The Cleft palate-craniofacial journal : officia...
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Thema
23
Journal Article
Research Support, Non-U.S. Gov't
4
Case Reports
2
Biomarkers, Tumor
2
Comparative Study
2
Consensus Development Conference
2
EC 2.3.2.26
2
EC 2.3.2.27
2
EC 2.7.10.1
2
ErbB Receptors
2
HectD1 protein, human
2
Hectd1 protein, mouse
2
Ubiquitin-Protein Ligases
1
147336-22-9
1
23521W1S24
1
804826J2HU
1
Acetylcholinesterase
1
Actinomyces neuii
1
Adaptor Proteins, Vesicular Transport
1
Amoxicillin
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Erscheinungszeitraum
4
2020-
12
2010-2019
7
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
23
Englisch
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