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C BRITT, R OLIVARES-NAVARRETE, JK WILLIAMS… - 2011 - iadr.confex.com
Introduction: Non-syndromic craniosynostosis is poorly understood and the molecular mechanisms
are not known. We hypothesized that cells in fused suture express higher levels of osteogenic
genes and produce paracrine factors that stimulate mesenchymal stem cells (MSCs) to ...
Cached
P Nieminen, NV Morgan, AL Fenwick… - American journal of …, 2011 - ncbi.nlm.nih.gov
Craniosynostosis and supernumerary teeth most often occur as isolated developmental
anomalies, but they are also separately manifested in several malformation syndromes.
Here, we describe a human syndrome featuring craniosynostosis, maxillary hypoplasia, ...
SA Rottgers, PD Kim, AR Kumar, JJ Cray… - Neurosurgical …, 2011 - medscape.com
Object Sagittal craniosynostosis is the most common form of craniosynostosis and is commonly
treated within the first year of life. Optimal treatment of patients older than 1 year of age is not
well characterized. The authors reviewed cases of sagittal craniosynostosis involving ...
A Beenken… - 2011 - content.karger.com
Abstract: Many craniosynostosis and dwarfism syndromes are attributable to gain-of-function
mutations in FGFR1, FGFR2, and FGFR3. The molecular bases by which these pathogenic mutations
over-activate FGFRs have been characterized extensively through the use of X-ray ...
Related articles
JRW Kestle… - 2011 - content.lib.utah.edu
Object. Childhood radiation exposure increases the lifetime risk of cancer from an estimated
0.07 to 0.35%. Neurological evaluation of patients after cranial vault reconstruction for synostosis
repair is often complicated by pain medication, sedation, intubation, swelling, and ...
Cached
C BRITT, R OLIVARES-NAVARRETE, JK WILLIAMS… - 2011 - iadr.confex.com
Introduction: Non-syndromic craniosynostosis is poorly understood and the molecular mechanisms
are not known. We hypothesized that cells in fused suture express higher levels of osteogenic
genes and produce paracrine factors that stimulate mesenchymal stem cells (MSCs) to ...
Cached
P Nieminen, NV Morgan, AL Fenwick… - American journal of …, 2011 - ncbi.nlm.nih.gov
Craniosynostosis and supernumerary teeth most often occur as isolated developmental
anomalies, but they are also separately manifested in several malformation syndromes.
Here, we describe a human syndrome featuring craniosynostosis, maxillary hypoplasia, ...
SA Rottgers, PD Kim, AR Kumar, JJ Cray… - Neurosurgical …, 2011 - medscape.com
Object Sagittal craniosynostosis is the most common form of craniosynostosis and is commonly
treated within the first year of life. Optimal treatment of patients older than 1 year of age is not
well characterized. The authors reviewed cases of sagittal craniosynostosis involving ...
A Beenken… - 2011 - content.karger.com
Abstract: Many craniosynostosis and dwarfism syndromes are attributable to gain-of-function
mutations in FGFR1, FGFR2, and FGFR3. The molecular bases by which these pathogenic mutations
over-activate FGFRs have been characterized extensively through the use of X-ray ...
Related articles
JRW Kestle… - 2011 - content.lib.utah.edu
Object. Childhood radiation exposure increases the lifetime risk of cancer from an estimated
0.07 to 0.35%. Neurological evaluation of patients after cranial vault reconstruction for synostosis
repair is often complicated by pain medication, sedation, intubation, swelling, and ...
Cached

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