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Results for
""5-Aminolevulinate Synthetase""[mesh_terms]

19 Results

Searching titles within these results

MiR-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 Cells.

Xunong Dong, Hongzhu Qu, Zhaojun Zhang, Xiangdong Fang, Nan Ding, Jiawen Zheng, Heyuan Qi, Yadong Yang, Hongying Sun, Yanming Li, Shuge Liu

International journal of molecular sciences 2016;16(12):28156-68

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Molecular pathophysiology and genetic mutations in congenital sideroblastic anemia.

Tohru Fujiwara, Hideo Harigae

Free radical biology & medicine 2020;133():179-185

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Experimental and approved treatments for skin photosensitivity in individuals with erythropoietic protoporphyria or X-linked protoporphyria: A systematic review.

Ida M Heerfordt, Catharina M Lerche, Peter A Philipsen, Hans Christian Wulf

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2023;158():114132

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Multiple mechanisms for hereditary sideroblastic anemia.

Shigeru Sassa, Kazumichi Furuyama

Cellular and molecular biology (Noisy-le-Grand, France) 2002;48(1):5-10

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5-Aminolevulinate synthase catalysis: The catcher in heme biosynthesis.

Bosko M Stojanovski, Gregory A Hunter, Insung Na, Vladimir N Uversky, Rays H Y Jiang, Gloria C Ferreira

Molecular genetics and metabolism 2020;128(3):178-189

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Severe iron overload with a novel aminolevulinate synthase mutation and hepatitis C infection. A case report.

Ernest Beutler, John J McCarthy, Lawrence Rice, Pauline Lee

Blood cells, molecules & diseases 2009;42(1):1-4

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X-linked sideroblastic anaemia in a female fetus: a case report and a literature review.

Diane Nzelu, Panicos Shangaris, Lisa Story, Frances Smith, Chinthika Piyasena, Jayanthi Alamelu, Amira Elmakky, Maria Pelidis, Rachel Mayhew, Srividhya Sankaran

BMC medical genomics 2022;14(1):296

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A hemizygous p.R204Q mutation in the ALAS2 gene underlies X-linked sideroblastic anemia in an adult Chinese Han man.

Jinbo Huang, Meili Ge, Yingqi Shao, Min Wang, Peng Jin, Jiali Huo, Xingxin Li, Jing Zhang, Neng Nie, Yizhou Zheng

BMC medical genomics 2024;14(1):107

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Erythropoietic Protoporphyria and X-Linked Protoporphyria: pathophysiology, genetics, clinical manifestations, and management.

Manisha Balwani

Molecular genetics and metabolism 2020;128(3):298-303

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In ferrochelatase-deficient protoporphyria patients, ALAS2 expression is enhanced and erythrocytic protoporphyrin concentration correlates with iron availability.

Elisabeth I Minder, Carina Schubiger, Gianfranco Biolcati, Xiaoye Schneider-Yin, Jasmin Barman-Aksözen

Blood cells, molecules & diseases 2015;54(1):71-7

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Regulatory network of tetrapyrrole biosynthesis--studies of intracellular signalling involved in metabolic and developmental control of plastids.

B Grimm, J Papenbrock

Planta 2002;213(5):667-81

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Alterations of heme metabolism in lymphocytes and metal content in blood plasma as markers of diesel fuels effects on human organism.

T Veidebaum, V Muzyka, S Bogovski, A Viitak

The Science of the total environment 2002;286(1-3):73-81

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The porphyrias: advances in diagnosis and treatment.

Manisha Balwani, Robert J Desnick

Hematology. American Society of Hematology. Education Program 2013;2012():19-27

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mRNA biomarkers sensitive and specific to micro-dose erythropoietin treatment at sea level and altitude.

Francesco Loria, Andreas Breenfeldt Andersen, Jacob Bejder, Thomas Bonne, Silke Grabherr, Tiia Kuuranne, Nicolas Leuenberger, Nikolai Baastrup Nordsborg

Drug testing and analysis 2024;16(11):1392-1401

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Three kinships with ALAS2 P520L (c. 1559 C --> T) mutation, two in association with severe iron overload, and one with sideroblastic anemia and severe iron overload.

Pauline L Lee, James C Barton, Sreenivas V Rao, Ronald T Acton, Brian K Adler, Ernest Beutler

Blood cells, molecules & diseases 2007;36(2):292-7

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Results: 1 – 15 / 19

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Results for ""5-Aminolevulinate Synthetase""[mesh_terms]

MiR-218 Inhibits Erythroid Differentiation and Alters Iron Metabolism by Targeting ALAS2 in K562 Cells.

Molecular pathophysiology and genetic mutations in congenital sideroblastic anemia.

Experimental and approved treatments for skin photosensitivity in individuals with erythropoietic protoporphyria or X-linked protoporphyria: A systematic review.

Multiple mechanisms for hereditary sideroblastic anemia.

5-Aminolevulinate synthase catalysis: The catcher in heme biosynthesis.

Severe iron overload with a novel aminolevulinate synthase mutation and hepatitis C infection. A case report.

X-linked sideroblastic anaemia in a female fetus: a case report and a literature review.

A hemizygous p.R204Q mutation in the ALAS2 gene underlies X-linked sideroblastic anemia in an adult Chinese Han man.

Erythropoietic Protoporphyria and X-Linked Protoporphyria: pathophysiology, genetics, clinical manifestations, and management.

In ferrochelatase-deficient protoporphyria patients, ALAS2 expression is enhanced and erythrocytic protoporphyrin concentration correlates with iron availability.

Regulatory network of tetrapyrrole biosynthesis--studies of intracellular signalling involved in metabolic and developmental control of plastids.

Alterations of heme metabolism in lymphocytes and metal content in blood plasma as markers of diesel fuels effects on human organism.

The porphyrias: advances in diagnosis and treatment.

mRNA biomarkers sensitive and specific to micro-dose erythropoietin treatment at sea level and altitude.

Three kinships with ALAS2 P520L (c. 1559 C --> T) mutation, two in association with severe iron overload, and one with sideroblastic anemia and severe iron overload.

Results for
""5-Aminolevulinate Synthetase""[mesh_terms]