The novel human MRC1 gene polymorphisms are associated with susceptibility to pulmonary tuberculosis in Chinese Uygur and Kazak populations

Polymorphic Allele of Human MRC1 Confer Protection against Tuberculosis in a Chinese Population

(2012) Xing Zhang et al.   International Journal of Biological Sciences

Association of TIRAP (MAL) gene polymorhisms with susceptibility to tuberculosis in a Chinese population

(2011) Y.X. Zhang et al.   GENETICS AND MOLECULAR RESEARCH

IL-10R1 S138G loss-of-function polymorphism is associated with extrapulmonary tuberculosis risk development in Tunisia

(2011) Walid Ben-Selma et al.   MOLECULAR BIOLOGY REPORTS

Genetic variants in mannose receptor gene (MRC1) confer susceptibility to increased risk of sarcoidosis

(2010) Takeshi Hattori et al.   BMC Medical Genetics

Lack of association between MD-2 promoter gene variants and tuberculosis

(2010) Y. Xue et al.   GENETICS AND MOLECULAR RESEARCH

Genetic and functional analysis of common MRC1 exon 7 polymorphisms in leprosy susceptibility

(2009) Andrea Alter et al.   HUMAN GENETICS

Genetic variants in the mannose receptor gene (MRC1) are associated with asthma in two independent populations

(2009) Takeshi Hattori et al.   IMMUNOGENETICS

Toll-like receptors 2 and 4 gene polymorphisms in a southeastern Chinese population with tuberculosis

(2009) Y. Xue et al.   International Journal of Immunogenetics

Association analysis of the PHOX2B gene with Hirschsprung disease in the Han Chinese population of Southeastern China

(2009) Cui-Ping Liu et al.   JOURNAL OF PEDIATRIC SURGERY

Common Nonsynonymous Polymorphisms in theNOD2Gene Are Associated with Resistance or Susceptibility to Tuberculosis Disease in African Americans

(2008) Celest M. Austin et al.   JOURNAL OF INFECTIOUS DISEASES

The Nod-Like Receptor (NLR) Family: A Tale of Similarities and Differences

(2008) Martina Proell et al.   PLoS One

Genetic Association and Expression Studies Indicate a Role of Toll-Like Receptor 8 in Pulmonary Tuberculosis

(2008) Sonia Davila et al.   PLoS Genetics