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Journal Articles

Gene-Selective Histone Hyperacetylation and Enhanced Sp1 Occupancy Underpin Transcriptional Modulation of Genes of the Glycolytic-Pentose Phosphate Pathway in Response to Histone Deacetylase Inhibitors - Therapeutic Implications

Kalliopi Makarona, Valentina Caputo, David Roper, Joana Costa, Gillian Cowan, Aristeidis Chaidos, David O'Connor, Elisabeth Georgiou, Maria Papaioannou, Mark Layton, Irene Roberts, Anastasios Karadimitris

Blood (2012) 120 (21): 977.

https://doi.org/10.1182/blood.V120.21.977.977

Published: 2012

Journal Articles

Cripto Regulates Hematopoietic Stem Cells As a Hypoxic Niche Related Factor Through the Cell Surface Receptor GRP78

Kenichi Miharada, Göran Karlsson, Matilda Rehn, Emma Rörby, Kavitha Siva, JÃ¶rg Cammenga, Stefan Karlsson, M.D., Ph.D., Prof.

Blood (2011) 118 (21): 2332.

https://doi.org/10.1182/blood.V118.21.2332.2332

Published: 2011

Journal Articles

A Novel Therapeutic Approach in Triosephosphate Isomerase Deficiency.

Christina Halsey, Solomon A. Ndoni, Roya Babaei-Jadidi, David Roper, Barbara J. Wild, Tom J. Vulliamy, Paul J. Thornalley, Mark Layton

Blood (2006) 108 (11): 3735.

https://doi.org/10.1182/blood.V108.11.3735.3735

Published: 2006

Journal Articles

Distinct behavior of mutant triosephosphate isomerase in hemolysate and in isolated form: molecular basis of enzyme deficiency

Ferenc Orosz, Judit Oláh, Marco Alvarez, György M. Keserű, Beáta Szabó, Gábor Wágner, Zoltán Kovári, Margit Horányi, Klára Baróti, Joseph A. Martial, Susan Hollán, Judit Ovádi

Blood (2001) 98 (10): 3106–3112.

https://doi.org/10.1182/blood.V98.10.3106

Published: 2001

Journal Articles

Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)

Colette Valentin, Serge Pissard, Josiane Martin, Delphine Héron, Philippe Labrune, Marie-Odile Livet, Michèle Mayer, Terri Gelbart, Arthur Schneider, Isabelle Max-Audit, Michel Cohen-Solal

Blood (2000) 96 (3): 1130–1135.

https://doi.org/10.1182/blood.V96.3.1130

Published: 2000

Journal Articles

Reversal of Metabolic Block in Glycolysis by Enzyme Replacement in Triosephosphate Isomerase–Deficient Cells

Art Ationu, Ann Humphries, Michel R.A. Lalloz, Roopen Arya, Barbara Wild, Joanne Warrilow, Jennifer Morgan, Alastair J. Bellingham, D. Mark Layton

Blood (1999) 94 (9): 3193–3198.

https://doi.org/10.1182/blood.V94.9.3193

Published: 1999

Journal Articles

The Relationship of the −5, −8, and −24 Variant Alleles in African Americans to Triosephosphate Isomerase (TPI) Enzyme Activity and to TPI Deficiency

Arthur Schneider, Linda Forman, Beryl Westwood, Catherine Yim, James Lin, Satinder Singh, Ernest Beutler

Blood (1998) 92 (8): 2959–2962.

https://doi.org/10.1182/blood.V92.8.2959

Published: 1998

NARROW

Gene-Selective Histone Hyperacetylation and Enhanced Sp1 Occupancy Underpin Transcriptional Modulation of Genes of the Glycolytic-Pentose Phosphate Pathway in Response to Histone Deacetylase Inhibitors - Therapeutic Implications

Cripto Regulates Hematopoietic Stem Cells As a Hypoxic Niche Related Factor Through the Cell Surface Receptor GRP78

A Novel Therapeutic Approach in Triosephosphate Isomerase Deficiency.

Distinct behavior of mutant triosephosphate isomerase in hemolysate and in isolated form: molecular basis of enzyme deficiency

Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)

Reversal of Metabolic Block in Glycolysis by Enzyme Replacement in Triosephosphate Isomerase–Deficient Cells

The Relationship of the −5, −8, and −24 Variant Alleles in African Americans to Triosephosphate Isomerase (TPI) Enzyme Activity and to TPI Deficiency

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ASH Publications

American Society of Hematology

Gene-Selective Histone Hyperacetylation and Enhanced Sp1 Occupancy Underpin Transcriptional Modulation of Genes of the Glycolytic-Pentose Phosphate Pathway in Response to Histone Deacetylase Inhibitors - Therapeutic Implications

Cripto Regulates Hematopoietic Stem Cells As a Hypoxic Niche Related Factor Through the Cell Surface Receptor GRP78

A Novel Therapeutic Approach in Triosephosphate Isomerase Deficiency.

Distinct behavior of mutant triosephosphate isomerase in hemolysate and in isolated form: molecular basis of enzyme deficiency

Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)

Reversal of Metabolic Block in Glycolysis by Enzyme Replacement in Triosephosphate Isomerase–Deficient Cells

The Relationship of the −5, −8, and −24 Variant Alleles in African Americans to Triosephosphate Isomerase (TPI) Enzyme Activity and to TPI Deficiency

Email alerts

ASH Publications

American Society of Hematology

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