Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Fatima Shaik"'
Publikováno v:
Neural Plasticity, Vol 2016 (2016)
Synaptic dysfunction is thought to play a major role in memory impairment in Alzheimer’s disease (AD). PARP-1 has been identified as an epigenetic regulator of plasticity and memory. Thus, we hypothesize that PARP-1 may be altered in postmortem hip
Externí odkaz:
https://doaj.org/article/993b7ccb79c04fb58430078b2b3a1410
Autor:
Stephen T. Melnick, Andrea M. Russo, Fatima Shaik, Matthew L. Ortman, Farooq A. Padder, John Andriulli
Publikováno v:
Journal of the American College of Cardiology. 81:185
Autor:
Emily P. Zeitler, Jeanne E. Poole, Christine M. Albert, Sana M. Al-Khatib, Fatima Ali-Ahmed, Ulrika Birgersdotter-Green, Yong-Mei Cha, Mina K. Chung, Anne B. Curtis, Jodie L. Hurwitz, Rachel Lampert, Roopinder K. Sandhu, Fatima Shaik, Erin Sullivan, Kamala P. Tamirisa, Annabelle Santos Volgman, Jennifer M. Wright, Andrea M. Russo
Publikováno v:
Circulation research. 130(4)
There is a growing appreciation for differences in epidemiology, treatment, and outcomes of cardiovascular conditions by sex. Historically, cardiovascular clinical trials have under-represented females, but findings have nonetheless been applied to c
Autor:
Rajasekhar, Maddirela Dilip, Badri, Kameswara Rao, Vinay Kumar, Kondeti, Kassetti, Ramesh Babu, Fatima, Shaik Sameena, Sampath Kumar, Mekala Thur, Appa Rao, Chippada
Publikováno v:
In Journal of Ethnopharmacology 2010 128(1):58-62
Publikováno v:
The American Journal of the Medical Sciences. 355:610-613
Thrombus in the heart is known to be one of the many sequelae of anterior wall myocardial infarction, atrial fibrillation and coagulation disorders. However, biventricular thrombi are relatively rarely found, even in conditions with a high possibilit
Autor:
Davi A. G. Mázala, Ravi Hindupur, Young Jae Moon, Fatima Shaikh, Iteoluwakishi H. Gamu, Dhruv Alladi, Georgiana Panci, Michèle Weiss-Gayet, Bénédicte Chazaud, Terence A. Partridge, James S. Novak, Jyoti K. Jaiswal
Publikováno v:
Cell Death Discovery, Vol 9, Iss 1, Pp 1-13 (2023)
Abstract Lack of dystrophin expression is the underlying genetic basis for Duchenne muscular dystrophy (DMD). However, disease severity varies between patients, based on specific genetic modifiers. D2-mdx is a model for severe DMD that exhibits exace
Externí odkaz:
https://doaj.org/article/ca9a535e1bfb4bc4a51860c19383424a
Publikováno v:
Infectious Diseases in Clinical Practice. 26:112-114
Publikováno v:
Neural Plasticity, Vol 2016 (2016)
Neural Plasticity
Neural Plasticity
Synaptic dysfunction is thought to play a major role in memory impairment in Alzheimer’s disease (AD). PARP-1 has been identified as an epigenetic regulator of plasticity and memory. Thus, we hypothesize that PARP-1 may be altered in postmortem hip
Publikováno v:
Cureus
We present the case of a patient with dilated cardiomyopathy caused by a novel mutation in the lysosome-associated membrane protein-2 (LAMP-2) gene. Patients with pathogenic mutations of this gene typically suffer from Danon disease – a condition t
Publikováno v:
The Physician and sportsmedicine. 10(6)