Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Reem Hasnah"'
Autor:
Melanie Makhlouf, Débora G. Souza, Smija Kurian, Bruna Bellaver, Hillary Ellis, Akihito Kuboki, Asma Al-Naama, Reem Hasnah, Gianina Teribele Venturin, Jaderson Costa da Costa, Neethu Venugopal, Diogo Manoel, Julie Mennella, Johannes Reisert, Michael G. Tordoff, Eduardo R. Zimmer, Luis R. Saraiva
Publikováno v:
Molecular Metabolism, Vol 79, Iss , Pp 101837- (2024)
Objective: Food processing greatly contributed to increased food safety, diversity, and accessibility. However, the prevalence of highly palatable and highly processed food in our modern diet has exacerbated obesity rates and contributed to a global
Externí odkaz:
https://doaj.org/article/ce678212020141b6b11a9d889ff82697
Autor:
Basma Haris, Saras Saraswathi, Sara Al‐Khawaga, Reem Hasnah, Amira Saeed, Shihab Mundekkadan, Noor Hamed, Houda Afyouni, Tasneem Abdel‐Karim, Shayma Mohammed, Amel Khalifa, Maryam Al‐Maadheed, Mahmoud Al‐Zyoud, Ahmed Shamekh, Ahmed Elawwa, Fawziya Al‐Khalaf, Sabri Boughorbel, Goran Petrovski, Khalid Hussain
Publikováno v:
Journal of Diabetes Investigation, Vol 12, Iss 12, Pp 2141-2148 (2021)
Abstract Aims/Introduction To study the epidemiology, genetic landscape and causes of childhood diabetes mellitus in the State of Qatar. Materials and methods All patients (aged 0–18 years) with diabetes mellitus underwent biochemical, immunologica
Externí odkaz:
https://doaj.org/article/f59812d4ddf14328951e013b926c3aef
The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar
Autor:
Sara Al‐Khawaga, Idris Mohammed, Saras Saraswathi, Basma Haris, Reem Hasnah, Amira Saeed, Hakeem Almabrazi, Najeeb Syed, Puthen Jithesh, Ahmed El Awwa, Amal Khalifa, Fawziya AlKhalaf, Goran Petrovski, Essam M. Abdelalim, Khalid Hussain
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Abstract Background Neonatal diabetes mellitus (NDM) is a rare condition that occurs within the first six months of life. Permanent NDM (PNDM) is caused by mutations in specific genes that are known for their expression at early and/or late stages of
Externí odkaz:
https://doaj.org/article/13c76bfb87ac45c783f1de1f50fc2ba4
Autor:
Sara Al-Khawaga, Jehan AlRayahi, Faiyaz Khan, Saras Saraswathi, Reem Hasnah, Basma Haris, Idris Mohammed, Essam M. Abdelalim, Khalid Hussain
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
The solute carrier family 16 member 1 (SLC16A1) gene encodes for monocarboxylate transporter 1 (MCT1) that mediates the movement of monocarboxylates, such as lactate and pyruvate across cell membranes. Inactivating recessive homozygous or heterozygou
Externí odkaz:
https://doaj.org/article/0f930b8dc61c4dfa987d6c99260dc52f
Autor:
Noor Hamed, Fawziya Al-Khalaf, Sara Al-Khawaga, Khalid Hussain, Tasneem Abdel-Karim, Goran Petrovski, Sabri Boughorbel, Reem Hasnah, Amira Saeed, Houda Afyouni, Shihab Mundekkadan, Ahmed Elawwa, Basma Haris, Maryam Al-Maadheed, Amel Khalifa, Saras Saraswathi, Mahmoud Alzyoud, Shayma Mohammed, Ahmed Shamekh
Publikováno v:
Journal of Diabetes Investigation, Vol 12, Iss 12, Pp 2141-2148 (2021)
Journal of Diabetes Investigation
Journal of Diabetes Investigation
Aims/Introduction To study the epidemiology, genetic landscape and causes of childhood diabetes mellitus in the State of Qatar. Materials and methods All patients (aged 0–18 years) with diabetes mellitus underwent biochemical, immunological and gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ac8f843d95bccae9b37b75e9e8335da
https://doaj.org/article/f59812d4ddf14328951e013b926c3aef
https://doaj.org/article/f59812d4ddf14328951e013b926c3aef
Publikováno v:
Oncotarget. 9:27171-27196
// Ali Abouelghar 1 , Reem Hasnah 2 , Ghina Taouk 3 , Mohamad Saad 4 and Manale Karam 5 1 Cancer Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Qatar Foundation, Doha, Qatar 2 Department of Biological Sciences, Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f713c4d9ddec58760b9f1a680fe29c28
https://doi.org/10.18632/oncotarget.25506
https://doi.org/10.18632/oncotarget.25506
Autor:
Satoshi Kubo, Jill M. Fritz, Hayley M. Raquer-McKay, Rhea Kataria, Ivan Vujkovic-Cvijin, Ahmad Al-Shaibi, Yikun Yao, Lixin Zheng, Juan Zou, Alex D. Waldman, Xinyi Jing, Taylor K. Farley, Ann Y. Park, Andrew J. Oler, Adrian K. Charles, Melanie Makhlouf, Eman H. AbouMoussa, Reem Hasnah, Luis R. Saraiva, Sundar Ganesan, Abdulrahman Ahmed Al-Subaiey, Helen Matthews, Emilio Flano, Hyun Hee Lee, Alexandra F. Freeman, Asena Pınar Sefer, Ersin Sayar, Erkan Çakır, Elif Karakoc-Aydiner, Safa Baris, Yasmine Belkaid, Ahmet Ozen, Bernice Lo, Michael J. Lenardo
Publikováno v:
Nature immunology. 23(1)
We report a pleiotropic disease due to loss-of-function mutations in RHBDF2, the gene encoding iRHOM2, in two kindreds with recurrent infections in different organs. One patient had recurrent pneumonia but no colon involvement, another had recurrent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10dfff11ac6fc2a78495279c1fbec6d2
https://pubmed.ncbi.nlm.nih.gov/34937930
https://pubmed.ncbi.nlm.nih.gov/34937930
Autor:
Luis R. Saraiva, Diogo Manoel, Richard C. Gerkin, Senthil Selvaraj, Abbirami Sathappan, Charles J. Arayata, Reem Hasnah, Sahar I. Da'as, Joel D. Mainland, Melanie Makhlouf, Doua Abdelrahman
Publikováno v:
Curr Biol
Odor perception in non-humans is poorly understood. Here, we generated the most comprehensive mouse olfactory ethological atlas to date, consisting of behavioral responses to a diverse panel of 73 odorants, including 12 at multiple concentrations. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b20a4405e858690996e435b87b005844
https://pubmed.ncbi.nlm.nih.gov/33957076
https://pubmed.ncbi.nlm.nih.gov/33957076
Autor:
Melanie Makhlouf, Doua Abdelrahman, Senthil Selvaraj, Richard C. Gerkin, Diogo Manoel, Abbirami Sathappan, Joel D. Mainland, Reem Hasnah, Charles J. Arayata, Saraiva Lr, Sahar I. Da'as
Odor perception in non-humans is poorly understood. Here, we generated the most comprehensive murine olfactory ethological atlas to date, consisting of behavioral responses to a diverse panel of 73 odorants, including 12 at multiple concentrations. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::062dd77141ace6866154b23e79e2bf71
https://doi.org/10.1101/2020.11.09.374637
https://doi.org/10.1101/2020.11.09.374637
The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the State of Qatar
Autor:
Amel Khalifa, Hakeem Almabrazi, Reem Hasnah, Saras Saraswathi, Essam M. Abdelalim, Basma Haris, Puthen V. Jithesh, Goran Petrovski, Idris Mohammed, Najeeb Syed, Fawziya Al-Khalaf, El Awwa A, Amira Saeed, Khalid Hussain, Sara Al-Khawaga
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Neonatal diabetes mellitus (NDM) is a rare condition that occurs within the first six months of life. Permanent NDM (PNDM) is caused by mutations in specific genes that are known for their expression at early and/or late stages of pancreat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a52056722207be2943e797383be9204
https://doi.org/10.1530/ey.17.2.10
https://doi.org/10.1530/ey.17.2.10