Ataxia telangiectasia gene mutations in leukaemia and lymphoma.

Ataxia telangiectasia gene mutations in leukaemia and lymphoma.

Ataxia telangiectasia (AT) is a rare multisystem, autosomal, recessive disease characterised by neuronal degeneration, genome instability, and an increased risk of cancer. Approximately 10% of AT homozygotes develop cancer, mostly of the lymphoid system. Lymphoid malignancies in patients with AT are...

Cur síos iomlán

Sonraí bibleagrafaíochta
Príomhchruthaitheoir:	Boultwood, J
Formáid:	Journal article
Teanga:	English
Foilsithe / Cruthaithe:	2001

Míreanna comhchosúla

MEK inhibitors block growth of lung tumors with mutations in Ataxia Telangiectasia Mutated
de réir: Smida, M, et al.
Foilsithe / Cruthaithe: (2016)

Phenotypic consequences of somatic mutations in the ataxia-telangiectasia mutated gene in non-small cell lung cancer
de réir: Weber, A, et al.
Foilsithe / Cruthaithe: (2016)

The role of declining ataxia-telangiectasia-mutated (ATM) function in oocyte aging
de réir: Suzuki, R, et al.
Foilsithe / Cruthaithe: (2024)

Risk of breast cancer and other cancers in heterozygotes for ataxia-telangiectasia.
de réir: Inskip, H, et al.
Foilsithe / Cruthaithe: (1999)

Odalisque's position as a geste antagoniste in a variant phenotype of ataxia-telangiectasia
de réir: Barrea, C, et al.
Foilsithe / Cruthaithe: (2019)

Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34.
de réir: Németh, A, et al.
Foilsithe / Cruthaithe: (2000)

Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?
de réir: Fogel, B, et al.
Foilsithe / Cruthaithe: (2015)

The epidemiology of leukaemias and lymphomas: a review.
de réir: Kinlen, L
Foilsithe / Cruthaithe: (1977)

Detection of individual differences in radiation-induced apoptosis of peripheral blood lymphocytes in normal individuals, ataxia telangiectasia homozygotes and heterozygotes, and breast cancer patients after radiotherapy.
de réir: Barber, J, et al.
Foilsithe / Cruthaithe: (2000)

Bevacizumab and type 1 idiopathic macular telangiectasia
de réir: Koay, C.L., et al.
Foilsithe / Cruthaithe: (2011)

Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
de réir: Boultwood, J, et al.
Foilsithe / Cruthaithe: (2009)

Phenotype and TCR-gamma gene rearrangements in a Malaysian cohort of T-cell leukaemia/lymphoma cases
de réir: Abdullah, Maha, et al.
Foilsithe / Cruthaithe: (2010)

Phenotype and TCR-gamma gene rearrangements in a Malaysian cohort of T-cell leukaemia/lymphoma cases
de réir: Maha, A., et al.
Foilsithe / Cruthaithe: (2010)

Presumed capillary telangiectasia of the pons: MRI and follow-up.
de réir: Küker, W, et al.
Foilsithe / Cruthaithe: (2000)

Mutations in PKC gamma in a UK family with spinocerebellar ataxia
de réir: Talbot, K, et al.
Foilsithe / Cruthaithe: (2005)

Midbrain ataxia.
de réir: Aziz, T, et al.
Foilsithe / Cruthaithe: (2005)

Dominant mutations in GRM1 cause spinocerebellar ataxia type 44
de réir: Watson, L, et al.
Foilsithe / Cruthaithe: (2017)

Familial exudative vitreoretinopathy mimicking macular telangiectasia type 1.
de réir: Simunovic, M, et al.
Foilsithe / Cruthaithe: (2014)

A master protocol to investigate a novel therapy acetyl-L-leucine for three ultra-rare neurodegenerative diseases: Niemann-Pick type C, the GM2 gangliosidoses, and ataxia telangiectasia
de réir: Fields, T, et al.
Foilsithe / Cruthaithe: (2021)

Candidate screening of the TRPC3 gene in cerebellar ataxia.
de réir: Becker, E, et al.
Foilsithe / Cruthaithe: (2011)

Candidate screening of the TRPC3 gene in cerebellar ataxia.
de réir: Becker, E, et al.
Foilsithe / Cruthaithe: (2011)

Epigenetic modification of the frataxin gene for the treatment of Friedreich’s ataxia
de réir: Vilema Enriquez, MG
Foilsithe / Cruthaithe: (2018)

Flash lamp pumped dye laser for rosacea-associated telangiectasia and erythema.
de réir: Lowe, N, et al.
Foilsithe / Cruthaithe: (1991)

Juvenile stroke in combined syndrome of hereditary hemorrhagic telangiectasia and juvenile polyposis
de réir: Mazzucco, S, et al.
Foilsithe / Cruthaithe: (2014)

Gastrointestinal: Massive intraperitoneal haemorrhage in a young woman with Hereditary Hemorrhagic telangiectasia
de réir: Sivarani, S., et al.
Foilsithe / Cruthaithe: (2010)

Genes for autosomal recessive cerebellar ataxia: order from chaos?
de réir: Nemeth, A, et al.
Foilsithe / Cruthaithe: (2001)

FOXP3, a selective marker for a subset of adult T-cell leukaemia/lymphoma.
de réir: Roncador, G, et al.
Foilsithe / Cruthaithe: (2005)

Distribution of childhood leukaemias and non-Hodgkin's lymphomas near nuclear installations in England and Wales.
de réir: Bithell, J, et al.
Foilsithe / Cruthaithe: (1994)

How do Gata1 and cohesin gene mutations contribute to the development of myeloid leukaemia?
de réir: Garnett, C
Foilsithe / Cruthaithe: (2020)

C/EBPalpha mutations in acute myeloid leukaemias.
de réir: Nerlov, C
Foilsithe / Cruthaithe: (2004)

Low expression of the putative tumour suppressor gene gravin in chronic myeloid leukaemia, myelodysplastic syndromes and acute myeloid leukaemia.
de réir: Boultwood, J, et al.
Foilsithe / Cruthaithe: (2004)

A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.
de réir: Isaacs, A, et al.
Foilsithe / Cruthaithe: (2003)

A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse
de réir: Isaacs, A, et al.
Foilsithe / Cruthaithe: (2003)

Next Generation Sequencing (NGS) of Genes Associated with Congenital and Neurodegenerative Ataxia
de réir: Kwasniewska, A, et al.
Foilsithe / Cruthaithe: (2011)

Effects of curcuma longa L. rhizomes in preventing the progression of carcinogenesis in leukaemia-lymphoma rats
de réir: Md Yusoff, Yusnaini
Foilsithe / Cruthaithe: (2013)

Can paternal preconceptional radiation account for the increase of leukaemia and non-Hodgkin's lymphoma in Seascale?
de réir: Kinlen, L
Foilsithe / Cruthaithe: (1993)

Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34
de réir: Moreira, M, et al.
Foilsithe / Cruthaithe: (2002)

Developing gene knockdown-replacement therapies for spinocerebellar ataxia type 7
de réir: Curtis, H, et al.
Foilsithe / Cruthaithe: (2013)

GATA1 mutational analysis in chronic myeloid leukaemia.
de réir: Halsey, C, et al.
Foilsithe / Cruthaithe: (2007)

Analysis of GATA-1 mutations in chronic myeloid leukaemia.
de réir: Halsey, C, et al.
Foilsithe / Cruthaithe: (2006)