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The Biochemical Journal
|
June 22, 2000
Identification and expression of NEU3, a novel human sialidase associated to the plasma membrane
E Monti, M T Bassi, N Papini, et al.
Genomics
|
December 1, 1994
Regional localization of 188 sequence tagged sites on a somatic cell hybrid mapping panel for human chromosome 3
R J Leach, R Chinn, B E Reus, et al.
Genomics
|
January 1, 1992
The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndrome
G Palmieri, V Capra, G Romano, et al.
Optics Express
|
February 7, 2018
Graded SiGe waveguides with broadband low-loss propagation in the mid infrared
J M Ramirez, Q Liu, V Vakarin, et al.
Human Molecular Genetics
|
December 15, 2000
Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1
M d'Addio, A Pizzigoni, M T Bassi, et al.
The New England Journal of Medicine
|
June 25, 1992
Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome
D Bick, B Franco, R J Sherins, et al.
Genomics
|
January 1, 1989
Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels
A Ballabio, R Carrozzo, G Parenti, et al.
Optics Express
|
April 7, 2017
Ge-rich graded-index Si<sub>1-</sub>xGex waveguides with broadband tight mode confinement and flat anomalous dispersion for nonlinear mid-infrared photonics
J M Ramirez, V Vakarin, J Frigerio, et al.
Transplantation Proceedings
|
December 1, 1994
Right hepatic artery replacement from superior mesenteric artery in combined liver-whole pancreas procurement. Technical problems and liver graft artery reconstruction
C V Sansalone, L De Carlis, G F Rondinara, et al.
Nature Genetics
|
June 1, 1996
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching
S Banfi, G Borsani, E Rossi, et al.
Page
of 20
Search research articles
Search
Showing results (131-140 of 200) with videos related to
Sort By:
Page
of 20
The Biochemical Journal
|
June 22, 2000
Identification and expression of NEU3, a novel human sialidase associated to the plasma membrane
E Monti, M T Bassi, N Papini, et al.
Genomics
|
December 1, 1994
Regional localization of 188 sequence tagged sites on a somatic cell hybrid mapping panel for human chromosome 3
R J Leach, R Chinn, B E Reus, et al.
Genomics
|
January 1, 1992
The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndrome
G Palmieri, V Capra, G Romano, et al.
Optics Express
|
February 7, 2018
Graded SiGe waveguides with broadband low-loss propagation in the mid infrared
J M Ramirez, Q Liu, V Vakarin, et al.
Human Molecular Genetics
|
December 15, 2000
Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1
M d'Addio, A Pizzigoni, M T Bassi, et al.
The New England Journal of Medicine
|
June 25, 1992
Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome
D Bick, B Franco, R J Sherins, et al.
Genomics
|
January 1, 1989
Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels
A Ballabio, R Carrozzo, G Parenti, et al.
Optics Express
|
April 7, 2017
Ge-rich graded-index Si<sub>1-</sub>xGex waveguides with broadband tight mode confinement and flat anomalous dispersion for nonlinear mid-infrared photonics
J M Ramirez, V Vakarin, J Frigerio, et al.
Transplantation Proceedings
|
December 1, 1994
Right hepatic artery replacement from superior mesenteric artery in combined liver-whole pancreas procurement. Technical problems and liver graft artery reconstruction
C V Sansalone, L De Carlis, G F Rondinara, et al.
Nature Genetics
|
June 1, 1996
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching
S Banfi, G Borsani, E Rossi, et al.
Page
of 20