Zobrazeno 1 - 10
of 252
pro vyhledávání: '"B. Pokhrel"'
Publikováno v:
Journal of Dairy Science, Vol 107, Iss 12, Pp 11139-11148 (2024)
ABSTRACT: Cow milk is rich in protein. Major cow milk proteins include αS1 casein (CSN1S1), αS2 casein (CSN1S2), β casein (CSN2), κ casein (CSN3), lactalbumin α (LALBA), and β-LG. These milk proteins are produced through gene expression in the
Externí odkaz:
https://doaj.org/article/395f48af84504ecca2e3ab499c4888fa
Publikováno v:
Atmospheric Chemistry and Physics, Vol 18, Pp 1325-1336 (2018)
The study of persistent organic pollutants (POPs) in low-latitude tropical and subtropical urban cities is necessary to assess their local and global impacts on ecosystems and human health. Despite studies on levels of POPs in water, soils, and se
Externí odkaz:
https://doaj.org/article/9aec5dcbe802471d92ec89d58e632711
Publikováno v:
Immunity, Inflammation and Disease, Vol 10, Iss 8, Pp n/a-n/a (2022)
Externí odkaz:
https://doaj.org/article/19e7a8312b27439ab47698257a07d302
Akademický článek
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Akademický článek
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Autor:
Jayan Man Shrestha, Sangam Rayamajhi, Samit Sharma, Naveen Chandra Bhatta, Nishan B Pokhrel, Biraj Pokhrel, Sandesh Gautam
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 1, Pp 198-202 (2021)
Clinical Case Reports, Vol 9, Iss 1, Pp 198-202 (2021)
Reduction mammoplasty with free nipple graft can be a good choice for early pubertal patients requiring massive reduction given its low recurrence and greater patient satisfaction.
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 11, Pp 2276-2280 (2020)
Clinical Case Reports, Vol 8, Iss 11, Pp 2276-2280 (2020)
Rare disease like primary spinal epidural diffuse large B‐cell lymphoma should be considered as a differential diagnosis in patients presenting with back pain and rapid neurological deterioration in the lower extremities.
Rare diseases like pr
Rare diseases like pr
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 12, Pp 2341-2345 (2020)
Clinical Case Reports, Vol 8, Iss 12, Pp 2341-2345 (2020)
β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation.
Publikováno v:
Clinical Case Reports, Vol 8, Iss 1, Pp 198-202 (2020)
Clinical Case Reports
Clinical Case Reports
Creutzfeldt‐Jakob disease (CJD) can also be diagnosed in a resource‐limited setting through good clinical analysis. The diagnosis of CJD should be considered in patients with rapidly evolving neurological signs associated with cognitive disturban
Publikováno v:
Proceeding of 7th Thermal and Fluids Engineering Conference (TFEC).