(Q43135419)

14 November 2017

Genetic characterization of acquired aplastic anemia by targeted sequencing (English)

1 reference

14 November 2017

1 reference

acquired aplastic anemia

1 reference

13

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14 November 2017

Michael Heuser

1

1 reference

14 November 2017

Carola Schlarmann

2

1 reference

14 November 2017

Vera Dobbernack

3

1 reference

14 November 2017

Victoria Panagiota

4

1 reference

14 November 2017

Lutz Wiehlmann

5

1 reference

14 November 2017

Carolin Walter

6

1 reference

14 November 2017

Fabian Beier

7

1 reference

14 November 2017

Patrick Ziegler

8

1 reference

14 November 2017

Haiyang Yun

9

1 reference

14 November 2017

Sofia Kade

10

1 reference

14 November 2017

Aylin Kirchner

11

1 reference

14 November 2017

Liu Huang

12

1 reference

14 November 2017

Matthias Eder

14

1 reference

14 November 2017

Tim H Brümmendorf

15

1 reference

14 November 2017

Martin Dugas

16

1 reference

14 November 2017

Arnold Ganser

17

1 reference

14 November 2017

Felicitas Thol

18

1 reference

14 November 2017

6 June 2014

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14 November 2017

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14 November 2017

99

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14 November 2017

9

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14 November 2017

e165-7

1 reference

Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia.

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

MYBL2 is a sub-haploinsufficient tumor suppressor gene in myeloid malignancy

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

Clonal diversity of recurrently mutated genes in myelodysplastic syndromes.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

Low frequency clonal mutations recoverable by deep sequencing in patients with aplastic anemia.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

MYBL2 haploinsufficiency increases susceptibility to age-related haematopoietic neoplasia.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

How I treat acquired aplastic anemia

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

Exome sequencing identifies MPL as a causative gene in familial aplastic anemia

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

Prognostic significance of ASXL1 mutations in patients with myelodysplastic syndromes

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

SNP array-based karyotyping: differences and similarities between aplastic anemia and hypocellular myelodysplastic syndromes.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

A method and server for predicting damaging missense mutations

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

Frequent epigenetic inactivation of the SLIT2 gene in chronic and acute lymphocytic leukemia

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

Acquired mutations in TET2 are common in myelodysplastic syndromes

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

SETBP1 mutation analysis in 944 patients with MDS and AML.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

A randomized controlled study in patients with newly diagnosed severe aplastic anemia receiving antithymocyte globulin (ATG), cyclosporine, with or without G-CSF: a study of the SAA Working Party of the European Group for Blood and Marrow Transplant

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4562551

Malignant tumors occurring after treatment of aplastic anemia. European Bone Marrow Transplantation-Severe Aplastic Anaemia Working Party

15 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24907358

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3324/HAEMATOL.2013.101642

1 reference

14 November 2017

1 reference

14 November 2017

PubMed publication ID

24907358

1 reference