Results 141 to 150 of about 2,894 (182)

Takotsubo Syndrome: The First Non-Acute Proteomic Analysis by Remote Dried Blood Microsampling. [PDF]

J Cardiovasc Transl Res
Marano P, Washington K, Chazarin B, Sundararaman N, Raedschelders K, Maughan J, Obrutu O, Tjoe B, Herscovici R, Moy P, Shufelt C, Rutledge T, Polyak A, Joung S, Liu Y, Cheng S, Wei J, Van Eyk JE, Merz CNB.   +18 more
europepmc   +1 more source

<i>Ex vivo</i> correction of severe coagulation Factor VII deficiency in patient-derived 3D liver organoids. [PDF]

Haematologica
Roman G, Lauritzen KH, Harrison SP, Bhattacharya A, Andresen MS, Mowinckel MC, Smolkova B, Henriksson CE, Glosli H, Iversen N, Thiede B, Sullivan GJ, Almaas R, Sandset PM, Stavik B, Chollet ME.   +15 more
europepmc   +1 more source

Supplement: FEBS-IUBMB-ENABLE 4^th International Molecular Biosciences, PhD and Postdoc Conference BRIDGING MINDS, Interdisciplinary research for the future of life sciences, 10^th-12^th September 2025, CRUK Scotland Institute, Glasgow, United Kingdom. [PDF]

FEBS Open Bio
europepmc   +1 more source

Structure and function of the EDEM:PDI ERAD checkpoint complex

Hitchman CJ, Lia A, Chiritoiu GN, Munteanu CVA, Ortigosa JR, Ghenea S, Savva C, Wada I, De Benedictis M, Tax G, Bayo Y, Crescioli I, Alonzi DL, Quigley A, Modenutti CP, Petrescu SM, Santino A, Gooptu B, Hosokawa N, Roversi P.   +19 more
europepmc   +1 more source

Convergent evolution of somatic escape variants inSERPINA1in the liver in alpha-1 anti-trypsin deficiency

Brzozowska N, Wu LY, Khodzhaeva V, Griffiths WJ, Duckworth A, Jung H, Coorens THH, Hooks Y, Chambers JE, Campbell PJ, Marciniak SJ, Hoare M.   +11 more
europepmc   +1 more source

Alpha1-antitrypsin (A1AT) accumulation in livers of emphysematous patients with A1AT deficiency

Human Pathology, 1972
Abstract An inherited deficiency of alpha 1 -antitrypsin (A 1 AT) in human serum predisposes to the development of pulmonary emphysema. A 1 AT is synthesized primarily by the liver, but no specific liver abnormality has been described in deficient subjects with lung disease. Fourteen of 17 livers from emphysematous patients with a Pi z variant of A 1
Herschel W. Gordon, James C. Dixon, James C. Rogers, Charles Mittman, Jack Lieberman   +4 more
openalex   +3 more sources

Alpha-1-Antitrypsin (A1AT) Proteotyping by LC-MS/MS

, 2023
The diagnosis of alpha-1-antitrypsin (A1AT) deficiency is established by quantitation of protein concentration in serum (immunoassay) followed by determination of specific allelic variants by phenotyping (isoelectric focusing (IEF) gel electrophoresis) and/or allele-specific genotyping.
Jennifer Kemp, Paula M. Ladwig, M Snyder
openalex   +3 more sources

Advanced Liver Disease in a Patient with PiMZ alpha-1 Antitrypsin (A1AT) Phenotype and Normal Serum A1AT Level

American Journal of Gastroenterology, 2007
Meena Narayanan, Swetha Kandula, Frank A. Mitros, Jatinder Ahluwalia   +3 more
openalex   +2 more sources