Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Imad, Salhab"'
Autor:
Nadine Alvarez, Gregory C. Adam, John A. Howe, Vijeta Sharma, Matthew D. Zimmerman, Enriko Dolgov, Risha Rasheed, Fatima Nizar, Khushboo Sahay, Andrew M. Nelson, Steven Park, Xiaoyan Zhou, Christine Burlein, John F. Fay, Daniel V. Iwamoto, Carolyn M. Bahnck-Teets, Krista L. Getty, Shih Lin Goh, Imad Salhab, Keith Smith, Christopher W. Boyce, Tamara D. Cabalu, Nicholas Murgolo, Nicholas G. Fox, Todd W. Mayhood, Valerie W. Shurtleff, Mark E. Layton, Craig A. Parish, John A. McCauley, David B. Olsen, David S. Perlin
Publikováno v:
Viruses, Vol 16, Iss 7, p 1158 (2024)
Severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) continues to be a global threat due to its ability to evolve and generate new subvariants, leading to new waves of infection. Additionally, other coronaviruses like Middle East respira
Externí odkaz:
https://doaj.org/article/5a441246ad714e97bc953aaa660b6bd5
Several reports emphasized the importance of inorganic pyrophosphate (PPi) in hindering osteoblast differentiation and bone matrix mineralization. Its ubiquitous presence is thought to prevent “soft” tissue calcification, whereas its degradation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3441a3d56e8666d80ac47aa51ea5545
https://doi.org/10.1101/2020.10.01.321976
https://doi.org/10.1101/2020.10.01.321976
Autor:
Imad Salhab, Philippe Krebs, Sungkyoung Lee, Russ P. Carstens, Matthew J. Sears, Zijun Zhang, Trevor Williams, Yi Xing, Hong Li, Hyun-Duck Nah
Publikováno v:
Development.
Cleft lip is one of the most common human birth defects. However, there remain a limited number of mouse models of cleft lip that can be leveraged to characterize the genes and mechanisms that cause this disorder. Crosstalk between epithelial and mes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b78170b3fd115d7b033e751d550c20c0
https://doi.org/10.1242/dev.187369
https://doi.org/10.1242/dev.187369
Autor:
Hyun-Duck Nah, Imad Salhab, Philippe Krebs, Sungkyoung Lee, Hong Li, Zijun Zhang, Matthew J. Sears, Trevor Williams, Yi Xing, Russ P. Carstens
Cleft lip is one of the most highly prevalent birth defects in human patients. However, there remain a limited number of mouse models of cleft lip and thus much work is needed to further characterize genes and mechanisms that lead to this disorder. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96ea42fe4c1c2c336c2aa98d7c5a3499
https://doi.org/10.1101/2019.12.12.874636
https://doi.org/10.1101/2019.12.12.874636
Autor:
SungKyoung, Lee, Matthew J, Sears, Zijun, Zhang, Hong, Li, Imad, Salhab, Philippe, Krebs, Yi, Xing, Hyun-Duck, Nah, Trevor, Williams, Russ P, Carstens
Publikováno v:
Development
Cleft lip is one of the most common human birth defects. However, there remain a limited number of mouse models of cleft lip that can be leveraged to characterize the genes and mechanisms that cause this disorder. Crosstalk between epithelial and mes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6506c07d9522a98134f431145f24a7d0
https://pubmed.ncbi.nlm.nih.gov/32253237
https://pubmed.ncbi.nlm.nih.gov/32253237
Autor:
Naiga Cottingham, Imad Salhab, Paul C. Billings, Rebekah S. Decker, Hyo Bin Um, Naito Kurio, Maurizio Pacifici, Cheri Saunders, Hyun-Duck Nah, Eiki Koyama, Till Edward Bechtold
Publikováno v:
Matrix Biology. :339-354
The temporomandibular joint (TMJ) is a diarthrodial joint that relies on lubricants for frictionless movement and long-term function. It remains unclear what temporal and causal relationships may exist between compromised lubrication and onset and pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f0ac3bc477ce4cfbc6afbe4c3946fc8
https://doi.org/10.1016/j.matbio.2016.03.001
https://doi.org/10.1016/j.matbio.2016.03.001
Publikováno v:
Journal of Endodontics. 42:480-486
Introduction The purpose of this study was to investigate odontogenic and osteogenic cell adhesion, proliferation, and survival on the surface of a newly developed bioceramic material (EndoSequence Root Repair Material [RRM]; Brasseler USA, Savannah,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd3d66bb4849c592b5bedd9888a1f855
https://doi.org/10.1016/j.joen.2015.11.013
https://doi.org/10.1016/j.joen.2015.11.013
Autor:
Imad Salhab, Eiki Koyama, Paul C. Billings, H. Um, Christina Mundy, Till Edward Bechtold, Cheri Saunders, Rebekah S. Decker, Naito Kurio, Hyun-Duck Nah, Maurizio Pacifici
Publikováno v:
Journal of Dental Research. 95:292-301
Heterotopic cartilage develops in certain pathologic conditions, including those affecting the human temporomandibular joint (TMJ), but the underlying molecular mechanisms remain obscure. This is in part due to the fact that a reliable animal model o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d5423cb257dac7f4ad473d432f93f2f
https://doi.org/10.1177/0022034515613508
https://doi.org/10.1177/0022034515613508
Autor:
Hyun-Duck Nah, Maurizio Pacifici, Ali Fakhry, Imad Salhab, Eiki Koyama, Charulatha Vedhachalam, Phoeby Leboy, Richard E. Kirschner, Chootima Ratisoontorn
Publikováno v:
Bone. 36:254-266
Systemically administered fibroblast growth factors (FGFs) show anabolic effects on bone formation in animals, whereas in vitro cell culture studies have demonstrated that FGFs block mineralized bone nodule formation. These apparently contradictory o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc50b4ba217970c28d5c07b96bd0cdca
https://doi.org/10.1016/j.bone.2004.10.003
https://doi.org/10.1016/j.bone.2004.10.003
Autor:
Melissa A. Radecki, Allison L. Zajac, Hyun-Duck Nah, Hakon Hakonarson, Imad Salhab, Sukwha Kim, Seung-Hak Baek
Publikováno v:
American journal of medical genetics. Part A. (3)
Craniometaphyseal dysplasia is caused by mutations in ANKH (ankylosis, progressive homolog [mouse]) in the majority of cases, and all of the reported mutations are single amino acid changes. Genomic DNA from an affected patient, his biological parent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::061b41a6fe0fd7ad957a8a9f36d72f15
https://pubmed.ncbi.nlm.nih.gov/20186813
https://pubmed.ncbi.nlm.nih.gov/20186813