Two novel somatic mutations of the ATRX gene in female patients with acquired alpha thalassemia of myelodysplastic syndrome (ATMDS).

Two novel somatic mutations of the ATRX gene in female patients with acquired alpha thalassemia of myelodysplastic syndrome (ATMDS).

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Haas, P, Schwabe, M, Fisher, C, Gibbons, R, Higgs, D, Bisse, E, Luebbert, M
التنسيق:	Conference item
منشور في:	2006

مواد مشابهة

Acquired alpha-thalassaernia in association with myelodysplastic syndrome (ATMDS): Two further private ATRX mutations
حسب: Fisher, C, وآخرون
منشور في: (2007)

Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.
حسب: Steensma, D, وآخرون
منشور في: (2004)

Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the alpha thalassemia myelodysplasia syndrome (ATMDS).
حسب: Gibbons, R, وآخرون
منشور في: (2003)

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).
حسب: Gibbons, R, وآخرون
منشور في: (2003)

The role of X-inactivation in the gender bias of patients with acquired alpha-thalassaemia and myelodysplastic syndrome (ATMDS).
حسب: Haas, P, وآخرون
منشور في: (2009)

DHPLC analysis of the ATRX gene in myelodysplastic syndrome (MDS) associated with acquired alpha thalassemia (AT-MDS): Novel mutation detection despite somatic mosaicism.
حسب: Steensma, D, وآخرون
منشور في: (2003)

A novel splicing mutation in the gene encoding the chromatin-associated factor ATRX associated with acquired hemoglobin H disease in myelodysplastic syndrome (ATMDS)
حسب: Steensma, D, وآخرون
منشور في: (2004)

Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the a thalassaemia myelodysplasia syndrome (ATMDS)
حسب: Gibbons, R, وآخرون
منشور في: (2003)

A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.
حسب: Costa, D, وآخرون
منشور في: (2006)

Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies.
حسب: Steensma, D, وآخرون
منشور في: (2005)

Deletion of the alpha-globin gene cluster as a cause of acquired alpha-thalassemia in myelodysplastic syndrome.
حسب: Steensma, D, وآخرون
منشور في: (2004)

Identification of mutations in ATRX by RNase mismatch cleavage.
حسب: Gibbons, R, وآخرون
منشور في: (1997)

5-Azacytidine treatment of the patient with ATMDS (vol 76, pg 432, 2006)
حسب: Costa, D, وآخرون
منشور في: (2006)

ATRX: taming tandem repeats.
حسب: Gibbons, R, وآخرون
منشور في: (2010)

Functional significance of mutations in the Snf2 domain of ATRX.
حسب: Mitson, M, وآخرون
منشور في: (2011)

The alpha-thalassemia/mental retardation syndromes.
حسب: Gibbons, R, وآخرون
منشور في: (1996)

PB2029: ACQUIRED ALPHA THALASSEMIA IN ASSOCIATION WITH MYELODYSPLASTIC SYNDROME- A CASE REPORT
حسب: Priyavadhana Balasubramanian, وآخرون
منشور في: (2023-08-01)

alpha-thalassaemia, X-linked mental retardation syndrome protein, ATRX, interacts with ribosomal genes.
حسب: Law, M, وآخرون
منشور في: (2003)

Mutations in the chromatin-associated protein ATRX.
حسب: Gibbons, R, وآخرون
منشور في: (2008)

Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX.
حسب: Argentaro, A, وآخرون
منشور في: (2007)

XNP/ATRX at sites of nucleosome replacement.
حسب: Garrick, D, وآخرون
منشور في: (2009)

A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy.
حسب: Guerrini, R, وآخرون
منشور في: (2000)

A Novel Mutation in ATRX Causes Alpha-Thalassemia X-Linked Intellectual Disability Syndrome in a Han Chinese Family
حسب: Shaomin Wu, وآخرون
منشور في: (2022-01-01)

α-Thalassemia, mental retardation, and myelodysplastic syndrome.
حسب: Gibbons, R
منشور في: (2012)

Acquired alpha thalassaemia in myelodysplastic syndrome
حسب: Cheong, P
منشور في: (2018)

The chromatin remodeller ATRX: A repeat offender in human disease
حسب: Clynes, D, وآخرون
منشور في: (2013)

The chromatin remodeller ATRX: a repeat offender in human disease.
حسب: Clynes, D, وآخرون
منشور في: (2013)

Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia
حسب: Steensma, D, وآخرون
منشور في: (2004)

Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia.
حسب: Steensma, D, وآخرون
منشور في: (2005)

Disruption of ATRX in mouse by conditional knockout.
حسب: Gibbons, R, وآخرون
منشور في: (2002)

The loss of ATRX increases susceptibility to pancreatic injury and oncogenic KRAS in female but not male mice
حسب: Young, C, وآخرون
منشور في: (2018)

X-linked alpha thalassaemia/mental retardation syndrome: a case with gonadal dysgenesis, caused by a novel mutation in ATRX gene.
حسب: Jezela-Stanek, A, وآخرون
منشور في: (2009)

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome).
حسب: Gibbons, R, وآخرون
منشور في: (1995)

ATRX and the replication of structured DNA.
حسب: Clynes, D, وآخرون
منشور في: (2013)

A nonsense mutation of the ATRX gene causing mild, moderate and profound mental retardation in members of a single family.
حسب: Gibbons, R, وآخرون
منشور في: (1999)

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.
حسب: Gibbons, R, وآخرون
منشور في: (2000)

THE ALPHA-THALASSEMIAS
حسب: Higgs, D, وآخرون
منشور في: (1990)

The alpha-thalassemias.
حسب: Higgs, D, وآخرون
منشور في: (1990)

Partial rescue of truncating mutations in the ATRX gene through unusual intra-exonic splicing
حسب: Malik, N, وآخرون
منشور في: (2006)

Melanesians and Polynesians share a unique alpha-thalassemia mutation.
حسب: Hill, A, وآخرون
منشور في: (1985)