Results 41 to 50 of about 499,908 (200)

Cellular Phenotypic Transformation in Heart Failure Caused by Coronary Heart Disease and Dilated Cardiomyopathy: Delineating at Single-Cell Level

open access: yesBiomedicines, 2022
Heart failure (HF) is known as the final manifestation of cardiovascular diseases. Although cellular heterogeneity of the heart is well understood, the phenotypic transformation of cardiac cells in progress of HF remains obscure.
Luojiang Zhu   +6 more
doaj   +1 more source

Robust Bayesian Variable Selection for Gene-Environment Interactions [PDF]

open access: yes, 2020
Gene-environment (G×E) interactions have important implications to elucidate the etiology of complex diseases beyond the main genetic and environmental effects.
Li, Xiaoxi, Ren, Jie, Wu, Cen, Zhou, Fei
core  

γ Heavy Chain Disease in Man: cDNA Sequence Supports Partial Gene Deletion Model [PDF]

open access: yes, 1982
Human gamma heavy chain disease (HCD) is characterized by the presence in serum of a short monoclonal Ig gamma chain unattached to light chains. Although most HCD proteins have internal deletions, in some the defect is NH2-terminal.
Alexander, Alice   +6 more
core  

Function of B cells expressing a human immunoglobulin M rheumatoid factor autoantibody in transgenic mice. [PDF]

open access: yes, 1993
We have generated transgenic mice that express the immunoglobulin (Ig)M heavy chain and kappa light chain genes coding for a human IgM rheumatoid factor (RF), Les.
Carson, DA   +6 more
core   +2 more sources

The peptide motif of the single dominantly expressed class I molecule of the chicken MHC can explain the response to a molecular defined vaccine of infectious bursal disease virus (IBDV) [PDF]

open access: yes, 2013
In contrast to typical mammals, the chicken MHC (the BF-BL region of the B locus) has strong genetic associations with resistance and susceptibility to infectious pathogens as well as responses to vaccines.
Butter, Colin   +4 more
core   +1 more source

Identification and genetic analysis of rare variants in myosin family genes in 412 Han Chinese congenital heart disease patients

open access: yesMolecular Genetics & Genomic Medicine, 2022
Background Myosin family genes, including those encoding myosin heavy chain 6, myosin heavy chain 7, myosin light chain 3, and myosin light chain 2 (MYL2), are important genetic factors in congenital heart disease (CHD).
Yunqian Zhang, Rui Peng, Hongyan Wang
doaj   +1 more source

The Evolution of Our Understanding of Immunoproliferative Small Intestinal Disease (IPSID) over Time

open access: yesCurrent Oncology, 2022
Immunoproliferative small intestinal disease (IPSID) is an uncommon disease with a higher prevalence in the developing world. IPSID diagnosis relies mainly on a tissue biopsy and a high index of suspicion.
Ruah AlYamany   +4 more
doaj   +1 more source

Prevalence of the E321G MYH1 variant for immune-mediated myositis and nonexertional rhabdomyolysis in performance subgroups of American Quarter Horses. [PDF]

open access: yes, 2019
BackgroundImmune-mediated myositis (IMM) in American Quarter Horses (QHs) causes acute muscle atrophy and lymphocytic infiltration of myofibers. Recently, an E321G mutation in a highly conserved region of the myosin heavy chain 1 (MYH1) gene was ...
Finno, Carrie J   +6 more
core   +2 more sources

Heavy chain deposition disease in a case of clear cell renal cell carcinoma- A jack in the box

open access: yesIndian Journal of Pathology and Microbiology, 2023
Renal cell carcinoma (RCC) is the most common subtype of adult renal tumors, and its detection rate in the early stages has been increased in the dawn of advanced imaging modalities.
Abhishek Kumar   +6 more
doaj   +1 more source

Heavy chain deposition disease presenting with raised anti-GBM antibody levels; a case report

open access: yesBMC Nephrology, 2020
Background Monoclonal immunoglobulin deposition disease (MIDD) is a rare condition accounting for
Michael Turner   +6 more
doaj   +1 more source

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