Results 61 to 70 of about 8,373,614 (131)

Cryo-EM structures of human ABCB7 reveal the molecular basis of mitochondrial matrix heme export

Communications Biology
ATP-binding cassette transporter subfamily B member 7 (ABCB7) is a mitochondrial ATP-driven pump essential for cytosolic iron–sulfur (Fe-S) cluster biogenesis and cellular iron homeostasis.
Seulgi Ju, Seung Hun Choi, Hyeon You Lee, Mi Sun Jin   +3 more
doaj   +1 more source

Socio‐Epidemiological Correlates of Anemia Among Non‐Pregnant Females of East and West Uttar Pradesh, India: A NFHS‐5 Secondary Data Analysis Highlighting the Need for Precision Public Policy

Public Health Challenges, Volume 4, Issue 3, September 2025.
ABSTRACT Anemia remains a persistent public health challenge in India, disproportionately affecting women and undermining maternal and reproductive health outcomes. Despite nationwide efforts, the burden of anemia continues to vary widely across regions, reflecting complex socio‐demographic determinants.
Sonam Maheshwari, Richa Sinha, Neil Patel, Okashah Kaiwan, Avisham Goyal, Oroshay Kaiwan, Inderbir Padda, Nidhi Uniyal, Mohammed K. Suhail, Talha Bin Emran, Nirja Kaka, Yashendra Sethi   +11 more
wiley   +1 more source

Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia

, 2003
The sideroblastic anemias are characterized by ring sideroblasts, that is, red cell precursors with mitochondrial iron accumulation. We therefore studied the expression of mitochondrial ferritin (MtF) in these conditions.
TRAVAGLINO E, BIASIOTTO, Giorgio, AROSIO, Paolo, CAZZOLA M, CORSI B, DRYSDALE J, INVERNIZZI R, BERGAMASCHI G, LEVI S, ROLANDI V   +9 more
core   +2 more sources

A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia [PDF]

, 2017
NDUFB11, a component of mitochondrial complex I, is a relatively small integral membrane protein, belonging to the 'supernumerary' group of subunits, but proved to be absolutely essential for the assembly of an active complex I.
Y. Guo, Lucarelli, Barbarella, M. Di Nottia, E.M. Valente, Di Nottia, M., Tartaglia, Marco, R. Carrozzo, Montanari, A, Bianchi, M, Bianchi, Marzia, Christodoulou, John, Rizza, T, Valente, EM, Sorrentino, F, Francisci, S., Torraco, Alessandra, Carrozzo, Rosalba, Martinelli, D, Sorrentino, F., Gelmetti, Vania, Gelmetti, V, Carrozzo, R., Rizza, T., Verrigni, D., Valente, Enza Maria, S. Francisci, Niceta, M., E. Bertini, Dionisi Vici, C., B. Lucarelli, M. Bianchi, F. Piemonte, Riley, Lisa, Christodoulou, J., L. Riley, Francisci, S, Bertini, E., D. Martinelli, Diodato, D, C. Dionisi‐Vici, J. Christodoulou, Piemonte, F, Niceta, Marcello, V. Gelmetti, A. Montanari, Di Nottia, Michela, T. Rizza, Guo, Yiran, Guo, Y., Piemonte, F., Riley, L., Martinelli, Diego, Sorrentino, Francesco, Torraco, A, Montanari, A., Niceta, M, Tartaglia, M., M. Niceta, BERTINI, Enrico, Christodoulou, J, Verrigni, D, Tartaglia, M, Dionisi-Vici, C, Carrozzo, R, Piemonte, Fiorella, Diodato, D., Lucarelli, B, Verrigni, Daniela, Bertini, E, Diodato, Daria, MONTANARI, Arianna, Martinelli, D., FRANCISCI, Silvia, Bianchi, M., D. Verrigni, Di Nottia, M, Rizza, Teresa, F. Sorrentino, Dionisi Vico, Carlo, M. Tartaglia, Torraco, A., Riley, L, Guo, Y, A. Torraco, Gelmetti, V., Lucarelli, B., D. Diodato   +86 more
core   +1 more source

Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females.

, 2000
X-linked sideroblastic anemia (XLSA) is caused by mutations in the erythroid-specific 5-aminolevulinic acid synthase (ALAS2) gene. An elderly woman who presented with an acquired sideroblastic anemia is studied.
CAZZOLA, MARIO, Bishop DF, Rosti V, BERGAMASCHI, GAETANO, Cerani P, May A   +5 more
core  

Zinc-Containing Over-The-Counter Product Causing Sideroblastic Anemia and Neutropenia [PDF]

Sideroblastic anemia is characterized by anemia, granulocytopenia, and bone marrow findings of vacuolated precursors and ringed sideroblasts. Zinc-induced copper deficiency can present as sideroblastic anemia and neutropenia.
Stagg, Marshall Patrick, Majid, Baseera, Polala, Ravali, Miatech, Jennifer   +3 more
core   +1 more source

A Case Report of Decompensated Cirrhosis of Liver with Sideroblastic Anemia. [PDF]

, 2015
UNLABELLED: A 35-year-old man was admitted to hospital with severe anemia. Two years back, he had presented with bleeding esophageal varices and subsequently diagnosed as a case of chronic liver disease with portal hypertension.
LutfulMubin, A, Rahman, S, Mahtab, M-A, Ahmad Khandokar, F, Mohammad Noor-E-Alam, S, Rahim, A   +5 more
core   +1 more source

Loss of function of mthsp70 chaperone variants leads to mitochondrial dysfunction in congenital sideroblastic anemia

, 2022
Congenital Sideroblastic Anemias (CSA) is a group of rare genetic disorders characterized by the abnormal accumulation of iron in erythrocyte precursors.
Vishwanathan, Vinaya, D’Silva, Patrick
core   +1 more source

A Novel Mutation of the Erythroid-Specific Aminolevulinate Synthase 2 Gene IN A Patient with Pyridoxine Responsive Sideroblastic Anemia and Deferasirox Responsive Hemochromatosis [PDF]

, 2009
A-14 years-old man, admitted to our clinic with weakness and paleness since one month. He has hepatosplenomegaly. Blood tests and peripheral blood smear showed anemia that severe hypochromic, microcytic anemia.
Tokgöz, Hüseyin, Çalışkan, Ümran, Yüksekkaya, Hasan   +2 more
core   +1 more source

Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source