APOA-I MILANO

ApoA-I Milano is a company that was acquired by The Medicines Company in 2009.

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APOA-I MILANO

Industry:
Internet

Founded:
2003-01-01

Status:
Active


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More informations about "ApoA-I Milano"

A consensus model of human apolipoprotein A-I in its โ€ฆ

Nov 13, 2017 Indeed, the natural mutations G26R in apoA-I IOWA 39 and R173C in apoA-I MILANO 40 both result in substantial decreases in free โ€ฆSee details»

Apolipoprotein AI - Wikipedia

As a major component of the high-density lipoprotein complex (protective "fat removal" particles), Apo-AI helps to clear fats, including cholesterol, from white blood cells within artery walls, making the white blood cells (WBCs) less likely to become fat overloaded, transform into foam cells, die and contribute to progressive atheroma. Five of nine men found to carry a mutation (E164X) who were at least 35 years of age had developed premature coronary artery disease. One of four muโ€ฆSee details»

Structural and functional consequences of the Milano mutation โ€ฆ

The introduction of a cysteine residue allows apoA-I to form apoA-I Milano (apoA-I M) homodimers or heterodimers with apoA-II . The apoA-I M mutation is located in the N-terminal โ€ฆSee details»

Secondary Structure Changes in ApoA-I Milano (R173C) Are Not ...

Described carriers of the Milano variant of apoA-I are heterozygotes and have very low plasma levels of apoA-I and HDL cholesterol as well as normal or moderately elevated plasma โ€ฆSee details»

Apolipoproteins in vascular biology and atherosclerotic disease

Oct 8, 2021 ApoA-I Milano is a naturally occurring genetic variant with an arginine-to-cysteine substitution at position 173. This genetic variant attracted attention because carriers had lower โ€ฆSee details»

Secondary Structure Changes in ApoA-I Milano (R173C) Are Not

Apr 22, 2014 Described carriers of the Milano variant of apoA-I are heterozygotes and have very low plasma levels of apoA-I and HDL cholesterol as well as normal or moderately elevated โ€ฆSee details»

Cardiovascular Status of Carriers of the Apolipoprotein A-I

Apr 17, 2001 The apolipoprotein A-I Milano (apoA-I M) mutation was described in 1980 in a family originating from Limone sul Garda in northern Italy. 1 This apoA-I variant shows a single โ€ฆSee details»

Apolipoprotein A-I: structureโ€“function relationships

Jun 1, 2000 ApoA-I is known to self-associate, a process which may stabilize the lipid-free protein. However, at low concentrations (below 0.1 mg/ml) (19), or in the presence of โ€ฆSee details»

Apolipoprotein A-I (ApoA-I), Immunity, Inflammation and Cancer

The first of these approaches can be accomplished by intravenous administration of autologous delipidated HDL, purified native ApoA-I, or recombinant ApoA-I Milano protein, a mutated โ€ฆSee details»

Effects of the Iowa and Milano Mutations on Apolipoprotein A-I ...

Nov 6, 2012 The Iowa point mutation in apolipoprotein A-I (G26R; apoA-I Iowa) leads to a systemic amyloidosis condition and the Milano mutation (R173C; apoA-I Mil) is associated with โ€ฆSee details»

Wild-Type ApoA-I and the Milano Variant Have Similar โ€ฆ

Jul 5, 2007 Patients presenting with the Milano mutation (R173C) of the apolipoprotein (apo) A-I, have significantly lower plasma HDL levels and paradoxically do not develop premature atherosclerosis. 1,2 The mechanism โ€ฆSee details»

Gene transfer of wild-type apoA-I and apoA-I Milano reduce ...

May 2, 2007 The human ApoA-I-Milano gene was cloned via site directed mutagenesis of the wtApoA-I plasmid by PCR. Correct cloning was confirmed by sequencing and restriction digests. To produce AAV vectors encapsidated in an AAV8 capsid (AAV2.8), a pseudotyping strategy was performed as reported [18,19]. Vectors were purified using a standard cesium ...See details»

ApoA-II Versus ApoA-I | Arteriosclerosis, Thrombosis, and Vascular โ€ฆ

Dec 1, 2001 ApoA-I Milano variant increases triglycerides in humans and transgenic mice: Increased because increased production and decreased clearance of VLDL: No effect: Plasma โ€ฆSee details»

Apo-AI (Apo-A1) Milano - GPnotebook

The decrease in apoA-I levels among individuals with these structural mutations is the result of rapid catabolism of apoA-I (1) apoA-I Milano (2) results in an average 40% decrease in apoA-I โ€ฆSee details»

Apolipoprotein A-I: structureโ€“function relationships

Feb 3, 2000 ApoA-I Milano (Arg 173 โ†’Cys), which has been extensively studied also appears to be associated with size restricted HDL lipoproteins (smaller HDL and reduced number of HDL โ€ฆSee details»

Apolipoprotein A-I (Milano): current perspectives - PubMed

Furthermore, recombinant apolipoprotein A-I(Milano) has displayed remarkable atheroprotective activities and the possibility of directly reducing the burden of atherosclerosis in experimental โ€ฆSee details»

The Long Saga of Apo-A1 Milano | Science - AAAS

Nov 16, 2016 It's been six years since I titled a post "Remember Apo-A1 Milano?" If you go back even further, I wrote about the topic on this blog back in 2003 (!); scroll down to the November โ€ฆSee details»

ApoA-I Infusion Therapies Following Acute Coronary Syndrome: โ€ฆ

May 7, 2022 MDCO-216 contains recombinant ApoA-I Milano, CER-001 contains recombinant wild-type human ApoA-I, and CSL111/CSL112 contains native ApoA-I isolated from human โ€ฆSee details»

ApoA-I Milano stimulates lipolysis in adipose cells independently โ€ฆ

ApoA-I Milano treatment induces rapid weight loss and increased lipolysis. C57bl6/J mice received one intraperitoneal injection/day of ApoA-I Milano (20 mg/kg), WT (20 mg/kg), or saline (NaCl), during 6 days (n = 6โ€“11 animals/group). Body weight was monitored daily during the treatment and 24 h after the last injection (day 0 first injection ...See details»

ApoA-I Milano/phospholipid complexes emerging pharmacological โ€ฆ

Recently, much attention has focused on a naturally occurring variant of apoA-I, apoA-I(Milano) (apoA-IM) characterized by a cysteine for arginine substitution that is associated with low rates of vascular disease and significant longevity in its carriers, despite markedly reduced HDL and elevated triglyceride levels.See details»

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