Language
English
German
^M
Dutch
Spanish
Title:
FGFR2 mutations in bent bone dysplasia syndrome activate nucleolar stress and perturb cell fate determination
Source:
Human Molecular Genetics [0964-6906] Neben, Cynthia yr:2017
Basic
Sorry, no full text available...
Please use the document delivery service (see below)
Holding information
Holdings in library search engine
ALBERT
Document delivery
Request document via
Library/Bibliothek
Users interested in this article also expressed an interest in the following:
description
1.
Scott, Richard H.
"The postnatal features of bent bone dysplasia-FGFR2 type."
Clinical dysmorphology
23.1 (2014): 8-11.
description
2.
Merrill, AE.
"Bent Bone Dysplasia Syndrome defines a nuclear role for FGFR2 in skeletal development."
The FASEB journal
27.S1 (2013).
description
3.
Moore, Gudrun B.
"Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome."
Nature Genetics
46.1 (2013): 70-76.
description
4.
Merrill, Amy E.
"Bent Bone Dysplasia-FGFR2 type, a Distinct Skeletal Disorder, Has Deficient Canonical FGF Signaling."
American journal of human genetics
90.3 (2012): 550-557.
description
5.
Merrill, AE.
"A novel skeletal disorder defines an intracellular role for FGFR2 during development."
The FASEB journal
26 (2012).
description
6.
Neben, Cynthia L.
"Bent bone dysplasia syndrome reveals nucleolar activity for FGFR2 in ribosomal DNA transcription."
Human molecular genetics
23.21 (2014): 5659-5671.
description
7.
"Standards for clinical use of genetic variants."
Nature Genetics
46.2 (2014): 93-93.
description
8.
Arthurs, Owen J.
"Routine perinatal and paediatric post-mortem radiography: detection rates and implications for practice."
Pediatric radiology
44.3 (2014): 252-7.
description
9.
Onoufriadis, A.
"Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm."
Journal of medical genetics
51.1 (2014): 61-67.
description
10.
Horvath, Günther E.
"Lipids of Mitochondria."
Progress in lipid research
52.4 (2013): 590-614.
description
11.
Kinsler, Veronica A.
"Multiple Congenital Melanocytic Naevi and Neurocutaneous Melanosis are Caused by Post-Zygotic Mutations in Codon 61 of NRAS."
Journal of investigative dermatology
133.9 (2013): 2229-2236.
description
12.
Altunkaynak, Bz.
"Effects of diabetes and ovariectomy on rat hippocampus (A biochemical and stereological study)."
Gynecological endocrinology
28.3 (2011): 228-233.
description
13.
Rachmiel, D.
"Mild Infantile Hypercalcemia: Diagnostic Tests and Outcomes."
The journal of pediatrics
159.2 (2011): 215-210.
description
14.
Pérez-Mancera, P A A.
"SLUG (SNAI2) overexpression in embryonic development."
Cytogenetic and genome research
114.1 (2006): 24-29.
description
15.
Yu, H.-L. A.
"Recent results on the spatiotemporal modelling and comparative analysis of Black Death and bubonic plague epidemics."
Public health
121.9 (2007): 700-720.
View More...
View Less...
Select All
Clear All
Save Citations
Select Format
ProCite
EndNote
RefWorks
Reference Manager
Submit citation export
Advanced
Author
Other articles by this author? -- in
GeoRef
author:
Neben, Cynthia L
Tuzon, Creighton T
Mao, Xiaojing
Lay, Fides D
Merrill, Amy E
last name
initials
Other articles by this author? -- in
Online Contents Geosciences
author:
Neben, Cynthia L
Tuzon, Creighton T
Mao, Xiaojing
Lay, Fides D
Merrill, Amy E
last name
initials
Other articles by this author? -- using
Web of Science
author:
Neben, Cynthia L
Tuzon, Creighton T
Mao, Xiaojing
Lay, Fides D
Merrill, Amy E
last name
initials
Web Search
Find related information in
a Web Search Engine
Excite
Google
HotBot
Ixquick
ZOO
Ask
Yahoo!
Bing
Naver
Search Terms:
Search for related information in
Google Scholar
Article Title
Author Name
Journal Title
Other Search
Search Terms:
A service provided by the
Library of the Wissenschaftspark Albert Einstein
, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.