The role of ABC transporters in ovarian cancer progression and chemoresistance

MP Ween, MA Armstrong, MK Oehler… - Critical reviews in …, 2015 - Elsevier
Over 80% of ovarian cancer patients develop chemoresistance which results in a lethal
course of the disease. A well-established cause of chemoresistance involves the family of …

Cobalamin coenzyme forms are not likely to be superior to cyano‐and hydroxyl‐cobalamin in prevention or treatment of cobalamin deficiency

R Obeid, SN Fedosov, E Nexo - Molecular nutrition & food …, 2015 - Wiley Online Library
Methylcobalamin (MeCbl) and adenosylcobalamin (AdoCbl) are coenzymes for methionine
synthase and methylmalonyl‐CoA mutase, respectively. Hydroxylcobalamin (HOCbl) and …

[PDF][PDF] Федеральные клинические рекомендации по оказания медицинской помощи детям с Желчекаменной болезнью

АА Баранов, ЛС Намазова-Баранова - МЗ РФ, Союз педиатров …, 2015 - astgmu.ru
Данные клинические рекомендации подготовлены совместно с Всероссийской
ассоциацией для больных муковисцидозом, рассмотрены и утверждены на заседании …

A review of vitamin B12 in dermatology

J Brescoll, S Daveluy - American journal of clinical dermatology, 2015 - Springer
Vitamin B12, also known as cobalamin, is a water-soluble vitamin that is important in the
hematological and nervous systems, and it has a complex relationship with the skin. Altered …

[HTML][HTML] Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines

M Huemer, V Kožich, P Rinaldo… - Journal of inherited …, 2015 - Springer
Newborn screening (NBS) is justified if early intervention is effective in a disorder generally
not detected early in life on a clinical basis, and if sensitive and specific biochemical markers …

Peroxisomal ABC transporters: functions and mechanism

A Baker, DJ Carrier, T Schaedler… - Biochemical Society …, 2015 - portlandpress.com
Peroxisomes are arguably the most biochemically versatile of all eukaryotic organelles.
Their metabolic functions vary between different organisms, between different tissue types of …

Insights into severe 5, 10‐methylenetetrahydrofolate reductase deficiency: molecular genetic and enzymatic characterization of 76 patients

P Burda, A Schäfer, T Suormala, T Rummel… - Human …, 2015 - Wiley Online Library
Methylenetetrahydrofolate reductase (MTHFR) deficiency is the most common inherited
disorder of folate metabolism and causes severe hyperhomocysteinaemia. To better …

Brg1 coordinates multiple processes during retinogenesis and is a tumor suppressor in retinoblastoma

I Aldiri, I Ajioka, B Xu, J Zhang, X Chen… - …, 2015 - journals.biologists.com
Retinal development requires precise temporal and spatial coordination of cell cycle exit,
cell fate specification, cell migration and differentiation. When this process is disrupted …

[HTML][HTML] Pathogenic mutations differentially affect the catalytic activities of the human B12-processing chaperone CblC and increase futile redox cycling

C Gherasim, M Ruetz, Z Li, S Hudolin… - Journal of Biological …, 2015 - ASBMB
Human CblC catalyzes the elimination of the upper axial ligand in cobalamin or B 12
derivatives entering the cell from circulation. This processing step is critical for assimilation …

Progressive hyperpigmentation in a Taiwanese child due to an inborn error of vitamin B12 metabolism (cblJ)

T Takeichi, CK Hsu, HS Yang, HY Chen… - British Journal of …, 2015 - academic.oup.com
The physiology of human skin pigmentation is varied and complex, with an extensive
melanogenic paracrine network involving mesenchymal and epithelial cells, contributing to …