Results 51 to 60 of about 131,340 (225)
In diabetic kidney disease, elevated podocyte ANGPTL4 is linked to reduced TFEB nuclear localization and compromised lysosomal degradative function. These changes impair podocyte lipophagy and promote lipid‐droplet accumulation and podocyte injury, which may contribute to renal injury progression.
Xiaojing Liu +7 more
wiley +1 more source
We describe a case of painless progressive loss of vision in a 15 years old male patient with Alport syndrome and diffuse Leiomyomatosis. After a comprehensive history and ocular examination, a diagnosis of bilateral posterior subcapsular cataracts was ...
Luis Santiago - Cabán +2 more
doaj +1 more source
Murine models of renal disease: Possibilities and problems in studies using mutant mice [PDF]
The elucidation of the pathogenesis of human renal disease at the molecular level has been facilitated by the growing field of gene targeting and the development of mouse strains with single-gene deletions - the `knock-out' mice. Experimental nephrology,
Anders, Hans-Joachim +1 more
core +1 more source
T‐Cell Remodeling in Renal Fibrosis: From Acute Injury to Chronic Kidney Disease
This Review presents renal fibrosis as a sequence of overlapping T‐cell programs, from chemokine‐guided recruitment and metabolic activation to maladaptive polarization, tertiary lymphoid structure formation, tissue residency, exhaustion, and senescence.
Qianhui Li +11 more
wiley +1 more source
ABSTRACT Current treatments for immune thrombocytopenia (ITP) and warm autoimmune hemolytic anemia (wAIHA), rare autoimmune diseases in which autoreactive B cells play a major role, can lead to high response rates; however, for many patients these responses are not durable or maintained after treatment discontinuation.
Matthieu Mahévas +4 more
wiley +1 more source
A construction for quasi-hereditary algebras [PDF]
Dlab V, Ringel CM. A construction for quasi-hereditary algebras. Compositio Mathematica.
Dlab, Vlastimil, Ringel, Claus Michael
core
Auslander algebras as quasi-hereditary algebras [PDF]
Dlab V, Ringel CM. Auslander algebras as quasi-hereditary algebras. Journal of the London Mathematical Society : Ser. 2.
Dlab, Vlastimil, Ringel, Claus Michael
core
Hereditary macrothrombocytopathia, deafness and nephritis (Epstein's triad)
PubMedID: 4055260Epstein's triad is a syndrome with a combination of hereditary macrothrombocytopathia and progressive sensorineural hearing loss and nephritis.
Mete R. +3 more
core +1 more source
A diagnosis confused with hereditary angioedema: nephrotic syndrome
Hereditary angioedema (HAE) is a rare, autosomal dominant disease that primarily affects the skin, upper respiratory tract, and gastrointestinal system.
Öykü Ünsal +4 more
doaj +1 more source
Autoantibodies against complement C1q in systemic lupus erythemathosus [PDF]
Complement and C1q, the first component of the classical pathway of activation of the complement system, are considered to be involved in the pathogenesis of systemic lupus erythematosus (SLE), a systemic autoimmune disease.
Bigler, Cornelia
core +1 more source

