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Forensic Science International. Genetics
|
October 17, 2024
Assessing the performance of multi-InDel panels for human identification among admixed Brazilians
Livia Carla Ramos, Luciellen D G Kobachuk, Douglas Mendes Nadur, et al.
Allergy
|
June 1, 2011
A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family
M F Ferraro, A S Moreno, E C Castelli, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 19, 2020
A large familial cluster and sporadic cases of frontal fibrosing alopecia in Brazil reinforce known human leucocyte antigen (HLA) associations and indicate new HLA susceptibility haplotypes
P M Ramos, L E F M Garbers, N S B Silva, et al.
International Journal of Legal Medicine
|
April 22, 2021
Prediction of eye and hair pigmentation phenotypes using the HIrisPlex system in a Brazilian admixed population sample
Thássia Mayra Telles Carratto, Letícia Marcorin, Guilherme do Valle-Silva, et al.
Molecular Genetics & Genomic Medicine
|
February 6, 2014
The +3187A/G HLA-G polymorphic site is associated with polar forms and reactive reaction in leprosy
N Lucena-Silva, M A G Teixeira, A de L Ramos, et al.
Molecular Immunology
|
August 25, 2018
Human leukocyte antigen-G 3' untranslated region polymorphisms are associated with asthma severity
Cinthia C Alves, Luísa K P Arruda, Fabíola R Oliveira, et al.
Immunogenetics
|
January 27, 2023
Comparison between qPCR and RNA-seq reveals challenges of quantifying HLA expression
Vitor R C Aguiar, Erick C Castelli, Richard M Single, et al.
Journal of Thrombosis and Haemostasis : JTH
|
January 26, 2010
Prothrombin G20210A carriers the genetic mutation and a history of venous thrombosis contributes to thrombin generation independently of factor II plasma levels
G Lavigne-Lissalde, C Sanchez, C Castelli, et al.
Human Immunology
|
November 21, 2024
The MICA deletion across different populations
Viviane Aparecida de Oliveira Ciriaco, Amanda Muniz Rodrigues, Brenda Caroline da Silva Tibúrcio, et al.
International Journal of Legal Medicine
|
August 21, 2025
Assessment of a microhaplotype panel for human identification and ancestry inference in Brazil
Luciellen Davila Giacomel Kobachuk, Vítor Matheus Soares Moraes, Thássia Mayra Telles Carratto, et al.
Page
of 24
Search research articles
Search
Showing results (171-180 of 236) with videos related to
Sort By:
Page
of 24
Forensic Science International. Genetics
|
October 17, 2024
Assessing the performance of multi-InDel panels for human identification among admixed Brazilians
Livia Carla Ramos, Luciellen D G Kobachuk, Douglas Mendes Nadur, et al.
Allergy
|
June 1, 2011
A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian family
M F Ferraro, A S Moreno, E C Castelli, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 19, 2020
A large familial cluster and sporadic cases of frontal fibrosing alopecia in Brazil reinforce known human leucocyte antigen (HLA) associations and indicate new HLA susceptibility haplotypes
P M Ramos, L E F M Garbers, N S B Silva, et al.
International Journal of Legal Medicine
|
April 22, 2021
Prediction of eye and hair pigmentation phenotypes using the HIrisPlex system in a Brazilian admixed population sample
Thássia Mayra Telles Carratto, Letícia Marcorin, Guilherme do Valle-Silva, et al.
Molecular Genetics & Genomic Medicine
|
February 6, 2014
The +3187A/G HLA-G polymorphic site is associated with polar forms and reactive reaction in leprosy
N Lucena-Silva, M A G Teixeira, A de L Ramos, et al.
Molecular Immunology
|
August 25, 2018
Human leukocyte antigen-G 3' untranslated region polymorphisms are associated with asthma severity
Cinthia C Alves, Luísa K P Arruda, Fabíola R Oliveira, et al.
Immunogenetics
|
January 27, 2023
Comparison between qPCR and RNA-seq reveals challenges of quantifying HLA expression
Vitor R C Aguiar, Erick C Castelli, Richard M Single, et al.
Journal of Thrombosis and Haemostasis : JTH
|
January 26, 2010
Prothrombin G20210A carriers the genetic mutation and a history of venous thrombosis contributes to thrombin generation independently of factor II plasma levels
G Lavigne-Lissalde, C Sanchez, C Castelli, et al.
Human Immunology
|
November 21, 2024
The MICA deletion across different populations
Viviane Aparecida de Oliveira Ciriaco, Amanda Muniz Rodrigues, Brenda Caroline da Silva Tibúrcio, et al.
International Journal of Legal Medicine
|
August 21, 2025
Assessment of a microhaplotype panel for human identification and ancestry inference in Brazil
Luciellen Davila Giacomel Kobachuk, Vítor Matheus Soares Moraes, Thássia Mayra Telles Carratto, et al.
Page
of 24