Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Meenakshi, Umar"'
Autor:
Jacques Courseault, Meenakshi Umar, Patrick Bordnick, Jocelyn Simons, Milla Volic, Allison Stock, Gregory Bix
Publikováno v:
ACR Open Rheumatology, Vol 6, Iss 7, Pp 399-402 (2024)
Objective Hypermobile Ehlers‐Danlos syndrome (hEDS) and hypermobility spectrum disorders (HSD) are characterized by joint hypermobility, joint subluxations and dislocations, hyperextensible skin, and chronic and progressive multiorgan comorbidities
Externí odkaz:
https://doaj.org/article/b3dac1a5e67d4190b52d290b9c9b8939
Autor:
Meenakshi Umar, Garrett Bartoletti, Chunmin Dong, Apurva Gahankari, Danielle Browne, Alastair Deng, Josue Jaramillo, Mimi Sammarco, Jennifer Simkin, Fenglei He
Publikováno v:
Developmental Dynamics. 252:589-604
Mammalian calvarium is composed of flat bones developed from two origins, neural crest and mesoderm. Cells from both origins exhibit similar behavior but express distinct transcriptomes. It is intriguing to ask whether genes shared by both origins pl
Publikováno v:
genesis.
Autor:
Meenakshi Umar, Garrett Bartoletti, Chunmin Dong, Apurva Gahankari, Danielle Browne, Alastair Deng, Josue Jaramillo, Mimi Sammarco, Jennifer Simkin, Fenglei He
Publikováno v:
SSRN Electronic Journal.
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e81999 (2013)
BACKGROUND:Tumour necrosis factor-alpha (TNF-α) and nuclear factor of kappa light chain gene enhancer in activated B cells (NF-κB) play critical role in carcinogenesis processes like tumour initiation, proliferation, migration and invasion. Single
Externí odkaz:
https://doaj.org/article/a337923a4c7a4ce2a309468d1396da13
Autor:
Meenakshi, Umar, Andre, Megarbane, Jingxuan, Shan, Najeeb, Syed, Eliane, Chouery, Elbay, Aliyev, Puthen, Jithesh, Ramzi, Temanni, Issam, Mansour, Lotfi, Chouchane, Aouatef, Ismail Chouchane
Publikováno v:
Journal of Cellular and Molecular Medicine
Familial Mediterranean fever (FMF) is the most common auto‐inflammatory disease. It is transmitted as autosomal recessive trait with mutations in MEditerranean FeVer (MEFV) gene. Despite a typical clinical expression, many patients have either a si
Publikováno v:
Dev Biol
The mammalian skull is composed of the calvarial bones and cartilages. Malformation of craniofacial cartilage has been identified in multiple human syndromes. However, the mechanisms of their development remain largely unknown. In the present study,
Autor:
Lauren Fidelak, Meenakshi Umar, Apurva Gahankari, Chunmin Dong, Fenglei He, Garrett Bartoletti
Publikováno v:
Gene Expr Patterns
Formation of the calvaria is a multi-staged process and is regulated by multiple genetic factors. Disruption of normal calvarial development usually causes craniosynostosis, a prevalent birth defect characterized by premature fusion of calvarial bone
Autor:
Meenakshi Umar, Alex Bittner, Wen-Jun Shen, Jackie Chan, Fredric B. Kraemer, Salman Azhar, Stefanie Bittner, Lu Han, Yuan Cortez, Dachuan Dong, Richard G. Peterson
Publikováno v:
Biochim Biophys Acta Mol Basis Dis
In recent years, the prevalence of obesity, metabolic syndrome and type 2 diabetes is increasing dramatically. They share pathophysiological mechanisms and often lead to cardiovascular diseases. The ZDSD rat was suggested as a new animal model to stu
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 6, p 1618 (2018)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
The classical function of Vitamin D, which involves mineral balance and skeletal maintenance, has been known for many years. With the discovery of vitamin D receptors in various tissues, several other biological functions of vitamin D are increasingl