The role of X-inactivation in the gender bias of patients with acquired alpha-thalassaemia and myelodysplastic syndrome (ATMDS).

The role of X-inactivation in the gender bias of patients with acquired alpha-thalassaemia and myelodysplastic syndrome (ATMDS).

Alpha thalassaemia myelodysplastic syndrome (ATMDS) is an unusual complication of chronic myeloid malignancy that is associated with a striking red cell phenotype. It represents an acquired form of alpha-thalassaemia that most commonly arises in the context of myelodysplasia. It has recently been sh...

Cur síos iomlán

Sonraí bibleagrafaíochta
Príomhchruthaitheoirí:	Haas, P, Roy, N, Gibbons, R, Deville, M, Fisher, C, Schwabe, M, Bissé, E, van Dorsselaer, A, Higgs, D, Lübbert, M
Formáid:	Journal article
Teanga:	English
Foilsithe / Cruthaithe:	2009

Míreanna comhchosúla

Acquired alpha-thalassaernia in association with myelodysplastic syndrome (ATMDS): Two further private ATRX mutations
de réir: Fisher, C, et al.
Foilsithe / Cruthaithe: (2007)

Two novel somatic mutations of the ATRX gene in female patients with acquired alpha thalassemia of myelodysplastic syndrome (ATMDS).
de réir: Haas, P, et al.
Foilsithe / Cruthaithe: (2006)

Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.
de réir: Steensma, D, et al.
Foilsithe / Cruthaithe: (2004)

Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the a thalassaemia myelodysplasia syndrome (ATMDS)
de réir: Gibbons, R, et al.
Foilsithe / Cruthaithe: (2003)

Acquired alpha thalassaemia in myelodysplastic syndrome
de réir: Cheong, P
Foilsithe / Cruthaithe: (2018)

A novel splicing mutation in the gene encoding the chromatin-associated factor ATRX associated with acquired hemoglobin H disease in myelodysplastic syndrome (ATMDS)
de réir: Steensma, D, et al.
Foilsithe / Cruthaithe: (2004)

Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the alpha thalassemia myelodysplasia syndrome (ATMDS).
de réir: Gibbons, R, et al.
Foilsithe / Cruthaithe: (2003)

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).
de réir: Gibbons, R, et al.
Foilsithe / Cruthaithe: (2003)

Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies.
de réir: Steensma, D, et al.
Foilsithe / Cruthaithe: (2005)

Alpha-thalassaemia.
de réir: Harteveld, C, et al.
Foilsithe / Cruthaithe: (2010)

The alpha thalassaemias.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (2009)

5-Azacytidine treatment of the patient with ATMDS (vol 76, pg 432, 2006)
de réir: Costa, D, et al.
Foilsithe / Cruthaithe: (2006)

Deletion of the alpha-globin gene cluster as a cause of acquired alpha-thalassemia in myelodysplastic syndrome.
de réir: Steensma, D, et al.
Foilsithe / Cruthaithe: (2004)

Alpha thalassaemia mental retardation (ATR-X): an atypical family.
de réir: Logie, L, et al.
Foilsithe / Cruthaithe: (1994)

DHPLC analysis of the ATRX gene in myelodysplastic syndrome (MDS) associated with acquired alpha thalassemia (AT-MDS): Novel mutation detection despite somatic mosaicism.
de réir: Steensma, D, et al.
Foilsithe / Cruthaithe: (2003)

The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia.
de réir: Vyas, P, et al.
Foilsithe / Cruthaithe: (1988)

X linked alpha thalassaemia/mental retardation: spectrum of clinical features in three related males.
de réir: Wilkie, A, et al.
Foilsithe / Cruthaithe: (1991)

alpha-thalassaemia, X-linked mental retardation syndrome protein, ATRX, interacts with ribosomal genes.
de réir: Law, M, et al.
Foilsithe / Cruthaithe: (2003)

Alpha thalassaemia in British people.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (1985)

Alpha thalassaemia-mental retardation, X linked
de réir: Gibbons, R
Foilsithe / Cruthaithe: (2006)

Alpha thalassaemia-mental retardation, X linked.
de réir: Gibbons, R
Foilsithe / Cruthaithe: (2006)

Alpha thalassaemia-mental retardation, X linked
de réir: Gibbons Richard
Foilsithe / Cruthaithe: (2006-05-01)

A newly defined X linked mental retardation syndrome associated with alpha thalassaemia.
de réir: Gibbons, R, et al.
Foilsithe / Cruthaithe: (1991)

The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage.
de réir: Donnai, D, et al.
Foilsithe / Cruthaithe: (1991)

Alpha-thalassaemia caused by a polyadenylation signal mutation.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (1983)

Screening of concurrent alpha-Thalassaemia 1 in beta-Thalassaemia carriers
de réir: Chong, Y.M., et al.
Foilsithe / Cruthaithe: (2006)

Alpha-thalassaemia in Nigeria: Its interaction with sickle-cell disease
de réir: Falusi, A, et al.
Foilsithe / Cruthaithe: (2009)

THE ALPHA-3.7 AND ALPHA-4.2 DELETION FORMS OF ALPHA+-THALASSAEMIA DIFFER IN SEVERITY
de réir: Hill, A, et al.
Foilsithe / Cruthaithe: (1985)

The non-deletion type of alpha thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritance.
de réir: Wilkie, A, et al.
Foilsithe / Cruthaithe: (1991)

Screening of Alpha-Thalassaemia 1 in Beta-Thalassaemia Carriers
de réir: Chong, Yi Min
Foilsithe / Cruthaithe: (2005)

Thalassaemia.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (2012)

Thalassaemia
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (2011)

A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.
de réir: Costa, D, et al.
Foilsithe / Cruthaithe: (2006)

Identification of a gain-of-function SNP causing a new model of alpha-thalassaemia.
de réir: De Gobbi, M, et al.
Foilsithe / Cruthaithe: (2005)

The interaction of alpha thalassaemia with malaria.
de réir: Oppenheimer, S, et al.
Foilsithe / Cruthaithe: (1987)

Alpha-thalassaemia and the malaria hypothesis.
de réir: Hill, A, et al.
Foilsithe / Cruthaithe: (1987)

α-thalassaemia
de réir: Higgs Douglas R, et al.
Foilsithe / Cruthaithe: (2010-05-01)

Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of alpha thalassaemia (--MED/(alpha)TSaudi(alpha)).
de réir: Viprakasit, V, et al.
Foilsithe / Cruthaithe: (2002)

Coupling ATMD System for Seismic Response Control of Two Adjacent Buildings
de réir: Kwan-Soon Park, et al.
Foilsithe / Cruthaithe: (2019-01-01)

Fundamental response in the vibration control of buildings subject to seismic excitation with ATMD
de réir: Fidel Jara Huanca, et al.
Foilsithe / Cruthaithe: (2023-07-01)