Zobrazeno 1 - 10
of 1 066
pro vyhledávání: '"A. G. Haddad"'
Autor:
Jayastu Senapati, Sanam Loghavi, Guillermo Garcia-Manero, Guillin Tang, Tapan Kadia, Nicholas J. Short, Hussein A. Abbas, Naszrin Arani, Courtney D. DiNardo, Gautam Borthakur, Naveen Pemmaraju, Betul Oran, Elizabeth Shpall, Uday Popat, Richard Champlin, Sherry Pierce, Sankalp Arora, Ghayas Issa, Musa Yilmaz, Keyur Patel, Koichi Takahashi, Guillermo Montalban-Bravo, Danielle Hammond, Fadi G. Haddad, Farhad Ravandi, Hagop M. Kantarjian, Naval G. Daver
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
In myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) with TP53 aberrations, dissecting the interaction amongst patient, disease and treatment factors are important for therapeutic decisions and prognostication. This retrospective analys
Externí odkaz:
https://doaj.org/article/c199f306952c4b93a7c1924a4e39b1b0
Publikováno v:
Turkish Journal of Hematology, Vol 32, Iss 1, Pp 80-81 (2015)
Externí odkaz:
https://doaj.org/article/370fa0fb2c3d49b2a3ee3b08326bebcb
Autor:
Fabio Papes, Antonio P. Camargo, Janaina S. de Souza, Vinicius M. A. Carvalho, Ryan A. Szeto, Erin LaMontagne, José R. Teixeira, Simoni H. Avansini, Sandra M. Sánchez-Sánchez, Thiago S. Nakahara, Carolina N. Santo, Wei Wu, Hang Yao, Barbara M. P. Araújo, Paulo E. N. F. Velho, Gabriel G. Haddad, Alysson R. Muotri
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-26 (2022)
Abstract Transcription Factor 4 (TCF4) has been associated with autism, schizophrenia, and other neuropsychiatric disorders. However, how pathological TCF4 mutations affect the human neural tissue is poorly understood. Here, we derive neural progenit
Externí odkaz:
https://doaj.org/article/7f4c4866201a4b0fb0158c28268eed74
Publikováno v:
Journal of Vascular Surgery Cases and Innovative Techniques, Vol 7, Iss 4, Pp 781-784 (2021)
Central venous obstruction in the symptomatic patient is often treated with endovascular stenting. A rare, but serious, complication of this treatment is migration of the stent from the original site of deployment. Treatment of this complication requ
Externí odkaz:
https://doaj.org/article/be9aa7f468c84a9bb0013721e8ddd419
Autor:
Magali Ranchou-Peyruse, Marion Guignard, Perla G. Haddad, Sylvain Robin, Fabrice Boesch, Maud Lanot, Hervé Carrier, David Dequidt, Pierre Chiquet, Guilhem Caumette, Pierre Cézac, Anthony Ranchou-Peyruse
Publikováno v:
Frontiers in Microbiology, Vol 13 (2023)
To be effective, microbiological studies of deep aquifers must be free from surface microbial contaminants and from infrastructures allowing access to formation water (wellheads, well completions). Many microbiological studies are based on water samp
Externí odkaz:
https://doaj.org/article/fb553a5abe6f43759311833f1a29fb5d
Autor:
Helen H. Zhao, Gabriel G. Haddad
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 16 (2022)
Introduction: Down syndrome (DS) is a genetic disorder with an extra copy of chromosome 21 and DS remains one of the most common causes of intellectual disabilities in humans. All DS patients have Alzheimer’s disease (AD)-like neuropathological cha
Externí odkaz:
https://doaj.org/article/13fa14f643b2471180fe5a4acbfc8383
Autor:
Wei Wu, Hang Yao, Priscilla D. Negraes, Juan Wang, Cleber A. Trujillo, Janaina S. de Souza, Alysson R. Muotri, Gabriel G. Haddad
Publikováno v:
Neurobiology of Disease, Vol 174, Iss , Pp 105882- (2022)
Early epilepsy is a prominent feature in patients with CDKL5-deficiency disorder (CDD). The underlying mechanism for excessive excitability in CDD is largely unknown. The brain organoid model has been recently developed to resemble many critical feat
Externí odkaz:
https://doaj.org/article/8d08b672563647ba9ad54e12609b20dd
Autor:
Libin Zhou, Kwangsik Nho, Maria G. Haddad, Nicole Cherepacha, Agne Tubeleviciute-Aydin, Andy P. Tsai, Andrew J. Saykin, P. Jesper Sjöström, Andrea C. LeBlanc
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-17 (2021)
Abstract Caspase-6 (Casp6) is implicated in Alzheimer disease (AD) cognitive impairment and pathology. Hippocampal atrophy is associated with cognitive impairment in AD. Here, a rare functional exonic missense CASP6 single nucleotide polymorphism (SN
Externí odkaz:
https://doaj.org/article/df2d07c515494ee380343cce22ca3145
Publikováno v:
BMC Pregnancy and Childbirth, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background The impact of using the Intergrowth (IG) dating formulae in comparison to the commonly used Robinson dating on the evaluation of biometrics and estimated fetal weight (EFW) has not been evaluated. Methods Nationwide cross-sectiona
Externí odkaz:
https://doaj.org/article/3030af28f8c24dc6af9d0d46c2400046
Autor:
Arya Iranmehr, Tsering Stobdan, Dan Zhou, Huiwen Zhao, Sergey Kryazhimskiy, Vineet Bafna, Gabriel G. Haddad
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
The genomic details of adaptation to extreme environments remain challenging to characterize. Using new methods to analyze flies experimentally evolved to survive extreme O2 conditions, the authors find a surprising level of synchronicity in selectiv
Externí odkaz:
https://doaj.org/article/2f35837d18f748b5835fa3f201891620