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Biochemistry
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July 13, 2000
Thermodynamic stability of the two isoforms of bovine seminal ribonuclease
C Giancola, P Del Vecchio, C De Lorenzo, et al.
Nanotechnology
|
January 27, 2018
Titanium contacts to graphene: process-induced variability in electronic and thermal transport
Keren M Freedy, Ashutosh Giri, Brian M Foley, et al.
Academic Pediatrics
|
September 16, 2024
Bringing Residents Back to the Bedside Through Trading Cards
Joshua A Belfer, Kinjal Desai, Hayley Wolfgruber, et al.
The Biochemical Journal
|
May 1, 1997
Effects of temperature and SDS on the structure of beta-glycosidase from the thermophilic archaeon Sulfolobus solfataricus
S D'auria, R Barone, M Rossi, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
July 14, 2016
New Codanin-1 Gene Mutations in a Italian Patient with Congenital Dyserythropoietic Anemia Type I and Heterozygous Beta-Thalassemia
Elena D'Alcamo, V Agrigento, L Pitrolo, et al.
Journal of Endocrinological Investigation
|
April 9, 1999
In vivo imaging of insulitis in autoimmune diabetes
A Signore, M Chianelli, M G Parisella, et al.
Minerva Chirurgica
|
October 9, 2002
[Cytoreductive surgery and intraperitoneal hyperthermic-antiblastic therapy (HAPP) in peritoneal carcinomatosis]
M Vaira, S Scuderi, D Costamagna, et al.
Genes and Immunity
|
December 4, 2003
A 24-bp duplication in exon 10 of human chitotriosidase gene from the sub-Saharan to the Mediterranean area: role of parasitic diseases and environmental conditions
L Malaguarnera, J Simporè, D A Prodi, et al.
Pediatrics
|
June 1, 1994
Evaluation of a rapid diagnostic test for respiratory syncytial virus (RSV): potential for bedside diagnosis
L R Krilov, S M Lipson, S R Barone, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Lysosomal enzyme activities in serum and leukocytes from patients with carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase deficiency)
R Barone, H Carchon, E Jansen, et al.
Page
of 22
Search research articles
Search
Showing results (151-160 of 217) with videos related to
Sort By:
Page
of 22
Biochemistry
|
July 13, 2000
Thermodynamic stability of the two isoforms of bovine seminal ribonuclease
C Giancola, P Del Vecchio, C De Lorenzo, et al.
Nanotechnology
|
January 27, 2018
Titanium contacts to graphene: process-induced variability in electronic and thermal transport
Keren M Freedy, Ashutosh Giri, Brian M Foley, et al.
Academic Pediatrics
|
September 16, 2024
Bringing Residents Back to the Bedside Through Trading Cards
Joshua A Belfer, Kinjal Desai, Hayley Wolfgruber, et al.
The Biochemical Journal
|
May 1, 1997
Effects of temperature and SDS on the structure of beta-glycosidase from the thermophilic archaeon Sulfolobus solfataricus
S D'auria, R Barone, M Rossi, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
July 14, 2016
New Codanin-1 Gene Mutations in a Italian Patient with Congenital Dyserythropoietic Anemia Type I and Heterozygous Beta-Thalassemia
Elena D'Alcamo, V Agrigento, L Pitrolo, et al.
Journal of Endocrinological Investigation
|
April 9, 1999
In vivo imaging of insulitis in autoimmune diabetes
A Signore, M Chianelli, M G Parisella, et al.
Minerva Chirurgica
|
October 9, 2002
[Cytoreductive surgery and intraperitoneal hyperthermic-antiblastic therapy (HAPP) in peritoneal carcinomatosis]
M Vaira, S Scuderi, D Costamagna, et al.
Genes and Immunity
|
December 4, 2003
A 24-bp duplication in exon 10 of human chitotriosidase gene from the sub-Saharan to the Mediterranean area: role of parasitic diseases and environmental conditions
L Malaguarnera, J Simporè, D A Prodi, et al.
Pediatrics
|
June 1, 1994
Evaluation of a rapid diagnostic test for respiratory syncytial virus (RSV): potential for bedside diagnosis
L R Krilov, S M Lipson, S R Barone, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Lysosomal enzyme activities in serum and leukocytes from patients with carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase deficiency)
R Barone, H Carchon, E Jansen, et al.
Page
of 22