Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Manu Jamwal"'
Autor:
Christine M. McDonald, Kenneth H. Brown, Yvonne E. Goh, Mari S. Manger, Charles D. Arnold, Nancy F. Krebs, Jamie Westcott, Julie M. Long, Rosalind S. Gibson, Manu Jamwal, Bidhi L. Singh, Neha Dahiya, Deepmala Budhija, Reena Das, Mona Duggal
Publikováno v:
BMC Nutrition, Vol 8, Iss 1, Pp 1-15 (2022)
Abstract Background Multiple micronutrient (MN) deficiencies remain highly prevalent among women of reproductive age (WRA) and preschool-aged children (PSC) in many areas within India. Salt is an attractive vehicle for MN fortification in this contex
Externí odkaz:
https://doaj.org/article/78f37524462c465f83f4eb12028a38f1
Autor:
Neetu Rani, Manu Jamwal, Jasbir Kaur, Pankaj Malhotra, Prashant Sharma, Arindam Maitra, Ranvir Singh, Subhash Varma, Reena Das
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue, Pp 85-85 (2017)
The krupple-like factor 1 (KLF1) is a crucial transcription factor that is responsible for the proper maturation of the erythroid cells. Recent studies have demonstrated that mutations in KLF1 gene may lead to increased fetal hemoglobin (HbF) and red
Externí odkaz:
https://doaj.org/article/6e68d641388e43c09b750069d139bdd5
Autor:
Manu Jamwal, Anu Aggarwal, Prashant Sharma, Deepak Bansal, Pankaj Malhotra, Arindam Maitra, Reena Das
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue, Pp 83-83 (2017)
Mutations in genes encoding red blood cell enzymes are often inherited in an autosomal recessive manner and can lead to chronic nonspherocytic hemolytic anemia (CNSHA) in homozygotes and compound heterozygotes. Usual clinical manifestations include j
Externí odkaz:
https://doaj.org/article/6e0093cb77324d3ca8cdeff8cb6bf0fb
Autor:
Anu Aggarwal, Manu Jamwal, Prashant Sharma, Man Updesh Singh Sachdeva, Pankaj Malhotra, Deepak Bansal, Reena Das
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue, Pp 84-84 (2017)
Hereditary spherocytosis (HS) is a common inherited hemolytic anemia characterized by the presence of microspherocytes. The pathogenesis involves defects in any of the several genes coding for membrane proteins that link the membrane skeleton to the
Externí odkaz:
https://doaj.org/article/5fb2062b0bc64928a6bbcadbd307c220
Publikováno v:
Nanotheranostics. 7:316-326
Autor:
Ritika Sharma, Manu Jamwal, Hari Kishan Senee, Namrata Singh, Narender Kumar, Chander Hans, Anita Kler, Deepak Bansal, Amita Trehan, Pankaj Malhotra, Jasmina Ahluwalia, Reena Das
Publikováno v:
Haemophilia. 29:591-599
Inherited Factor VII (FVII) deficiency is commonest among the rare bleeding disorders. A small number of patients present in infancy with severe bleeding, and many may remain asymptomatic but detected before surgery/invasive procedures. Genetic testi
Autor:
Ritika Sharma, Manu Jamwal, Namrata Singh, Prashant Sharma, Deepak Bansal, Amita Trehan, Pankaj Malhotra, Arihant Jain, Jasmina Ahluwalia, Reena Das, Narender Kumar
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 39:276-283
Autor:
McDonald, Yvonne E. Goh, Mari S. Manger, Mona Duggal, Reena Das, Shipra Saklani, Surbhi Agarwal, Deepmala Budhija, Manu Jamwal, Bidhi L. Singh, Neha Dahiya, Hanqi Luo, Julie M. Long, Jamie Westcott, Nancy F. Krebs, Rosalind S. Gibson, Kenneth H. Brown, Christine M.
Publikováno v:
Nutrients; Volume 15; Issue 13; Pages: 3024
Dietary intake and biomarkers of micronutrient status of 100 non-pregnant women of reproductive age (NPWRA) were assessed to determine optimal levels of iron, zinc, vitamin B12, and folic acid to include in multiply-fortified salt (MFS) that will be
Autor:
Ritika Sharma, Manu Jamwal, Namrata Singh, Prashant Sharma, Deepak Bansal, Amita Trehan, Pankaj Malhotra, Arihant Jain, Jasmina Ahluwalia, Reena Das, Narender Kumar
Publikováno v:
Indian J Hematol Blood Transfus
Autor:
Namrata Singh, Manu Jamwal, Ritika Sharma, Pooja Murgai, Sanjeev Chhabra, Jasbir Kaur Hira, Reena Das, Prashant Sharma
Publikováno v:
Annals of Hematology. 101:2799-2801