Disease Understanding Archives - Page 2 of 8

Disease mechanisms of X- linked cone dystrophy caused by missense mutations in the red and green cone opsins

April 9, 2022 Disease Understanding Comments Off on Disease mechanisms of X- linked cone dystrophy caused by missense mutations in the red and green cone opsins

Dynorphin Neuropeptides Decrease Apparent Proton Affinity of ASIC1a

March 23, 2022 Disease Understanding Comments Off on Dynorphin Neuropeptides Decrease Apparent Proton Affinity of ASIC1a

In vitro rejuvenation of osteoarthritis-affected human chondrocytes cultured in a polymer based 3D matrix, evidenced by enhanced miRNA expression

March 5, 2022 Disease Understanding Comments Off on In vitro rejuvenation of osteoarthritis-affected human chondrocytes cultured in a polymer based 3D matrix, evidenced by enhanced miRNA expression

Circadian control of heparan sulfate levels times clearance of amyloid beta aggregates

March 4, 2022 Disease Understanding Comments Off on Circadian control of heparan sulfate levels times clearance of amyloid beta aggregates

Impact of endocrine-disrupting chemicals on steroidogenesis and consequences on testicular function

February 15, 2022 Disease Understanding Comments Off on Impact of endocrine-disrupting chemicals on steroidogenesis and consequences on testicular function

Novel Endoxifen-Resistant Breast Cancer Cell Lines Highlight Numerous Differences from Tamoxifen-Resistant Models

January 28, 2022 Disease Understanding Comments Off on Novel Endoxifen-Resistant Breast Cancer Cell Lines Highlight Numerous Differences from Tamoxifen-Resistant Models

Heterogeneity of neutrophils in arterial hypertension

December 8, 2021 Disease Understanding Comments Off on Heterogeneity of neutrophils in arterial hypertension

Choline transporter-like proteins 1 and 2 are newly identified plasma membrane and mitochondrial ethanolamine transporters

November 13, 2021 Disease Understanding Comments Off on Choline transporter-like proteins 1 and 2 are newly identified plasma membrane and mitochondrial ethanolamine transporters

Mutations in EDA and EDAR genes cause dominant syndromic tooth agenesis

October 17, 2021 Disease Understanding Comments Off on Mutations in EDA and EDAR genes cause dominant syndromic tooth agenesis

Familial Alzheimer’s disease mutations in amyloid protein precursor alter proteolysis by γ-secretase to increase amyloid β-peptides of ≥45 residues

October 5, 2021 Disease Understanding Comments Off on Familial Alzheimer’s disease mutations in amyloid protein precursor alter proteolysis by γ-secretase to increase amyloid β-peptides of ≥45 residues