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Mechanisms of Development, ISSN 0925-4773, 07/2017, Volume 145, pp. S120 - S120
Journal Article
Mechanisms of Development, ISSN 0925-4773, 07/2017, Volume 145, pp. S123 - S123
Journal Article
Mechanisms of Development, ISSN 0925-4773, 07/2017, Volume 145, pp. S112 - S112
Journal Article
Mechanisms of Development, ISSN 0925-4773, 07/2017, Volume 145, p. S123
Journal Article
Journal of Cellular Biochemistry, ISSN 0730-2312, 11/2013, Volume 114, Issue 11, pp. 2437 - 2445
Journal Article
Mechanisms of Development, ISSN 0925-4773, 07/2017, Volume 145, pp. S118 - S118
Journal Article
Journal Article
Mechanisms of Development, ISSN 0925-4773, 07/2017, Volume 145, pp. S120 - S121
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2016, Volume 11, Issue 8, p. e0160691
Cataract is the most common cause of visual loss in humans. A spontaneously occurred, autosomal dominant mouse mutant Secc, which displayed combined features... 
Eye | Cataract | Gene mutations | Physiological aspects | Genetic aspects | Research | Diagnosis
Journal Article
Developmental Biology, ISSN 0012-1606, 09/2016, Volume 417, Issue 2, pp. 229 - 251
Journal Article
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, ISSN 0892-6638, 06/2019, Volume 33, Issue 6, pp. 6838 - 6851
The channel that governs mechanotransduction (MT) by hair cells in the inner ear has been investigated intensively for 4 decades, but its precise molecular... 
hearing | stereocilia | tip link | mechanotransduction channel | mechanotransduction complex | COMPLEX | PROTEIN | ESSENTIAL COMPONENT | BIOCHEMISTRY & MOLECULAR BIOLOGY | DOMINANT | CELL BIOLOGY | PROTOCADHERIN-15 | MECHANOTRANSDUCTION MACHINERY | CHANNEL | BIOLOGY | DEAFNESS | MUTATIONS | INNER
Journal Article
Clinical Oral Implants Research, ISSN 0905-7161, 03/2011, Volume 22, Issue 3, pp. 338 - 342
Objectives: To assess the influence of nicotine on the proliferation and gene expression of osteogenic and angiogenic mediators of osteoblasts. Material and... 
angiogenic mediator | nicotine | osteoblast | proliferation | osteogenic mediator | Osteoblast | Osteogenic mediator | Proliferation | Angiogenic mediator | Nicotine | CELLS | ENGINEERING, BIOMEDICAL | VEGF | DISTRACTION OSTEOGENESIS | RELEASE | SAOS-2 | VASCULAR SMOOTH-MUSCLE | CIGARETTE-SMOKING | DENTISTRY, ORAL SURGERY & MEDICINE | GENE-EXPRESSION | BONE REGENERATION | BLOOD | Neovascularization, Physiologic - drug effects | Rabbits | Bone Morphogenetic Protein 2 - drug effects | Nicotine - administration & dosage | Coloring Agents | Osteoblasts - drug effects | Osteogenesis - drug effects | Bone Morphogenetic Protein 2 - antagonists & inhibitors | Vascular Endothelial Growth Factor A - antagonists & inhibitors | Reverse Transcriptase Polymerase Chain Reaction | Nicotine - pharmacology | Tetrazolium Salts | Phenotype | Animals | Transforming Growth Factor beta - drug effects | Time Factors | Thiazoles | Transforming Growth Factor beta - antagonists & inhibitors | Platelet-Derived Growth Factor - drug effects | Cell Proliferation - drug effects | Cell Culture Techniques | Vascular Endothelial Growth Factor A - drug effects | Platelet-Derived Growth Factor - antagonists & inhibitors | Analysis | Universities and colleges | Gene expression | Vascular endothelial growth factor | Implant dentures | Growth factors | Endothelium | Angiogenesis
Journal Article
Gastroenterology, ISSN 0016-5085, 2015, Volume 149, Issue 7, pp. 1837 - 1848.e5
Background & Aims Hirschsprung disease is characterized by a deficit in enteric neurons, which are derived from neural crest cells (NCCs). Aberrant hedgehog... 
Gastroenterology and Hepatology | Nervous System Development | HSCR | Aganglionic Megacolon | Mouse Model | SOX10 EXPRESSION | CELLS | SONIC HEDGEHOG | PROLIFERATION | PALLISTER-HALL SYNDROME | NEURAL CREST DEVELOPMENT | MAINTENANCE | GENE | DIFFERENTIATION | GASTROENTEROLOGY & HEPATOLOGY | Wnt1 Protein - genetics | Humans | Neural Crest - pathology | Zinc Finger Protein Gli2 | Hirschsprung Disease - genetics | Zinc Finger Protein Gli3 | Male | Wnt1 Protein - metabolism | Mice, 129 Strain | DNA Mutational Analysis - methods | Enteric Nervous System - abnormalities | Neurogenesis | Case-Control Studies | Neural Crest - metabolism | Transfection | Gene Expression Regulation, Developmental | Kruppel-Like Transcription Factors - metabolism | Female | Nuclear Proteins - genetics | Repressor Proteins - metabolism | Disease Models, Animal | Genetic Predisposition to Disease | SOXE Transcription Factors - metabolism | Enteric Nervous System - metabolism | Mice, Inbred C57BL | Hirschsprung Disease - pathology | Repressor Proteins - genetics | Mice, Transgenic | Nuclear Proteins - metabolism | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Mice, Inbred ICR | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Cell Lineage | Hirschsprung Disease - diagnosis | Phenotype | Animals | High-Throughput Nucleotide Sequencing | Zinc Finger Protein GLI1 | HeLa Cells | Mutation | Hirschsprung Disease - metabolism | Kruppel-Like Transcription Factors - genetics | Cell Movement | SOXE Transcription Factors - genetics | Hirschsprung's disease | Genetic research | Genetic aspects | Analysis | Children's hospitals | Stem cells
Journal Article