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Cancer risk in relatives of patients with a primary disorder of lymphocyte cytotoxicity: a retrospective cohort study.
scientific article published on 3 December 2015
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Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
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3 March 2020
title
Cancer risk in relatives of patients with a primary disorder of lymphocyte cytotoxicity: a retrospective cohort study
(English)
1 reference
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Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
author
Samuel C Chiang
series ordinal
2
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Europe PubMed Central
PubMed publication ID
26686408
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
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3 March 2020
Yenan Bryceson
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4
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Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
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3 March 2020
Jan-Inge Henter
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6
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Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
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3 March 2020
author name string
Alexandra Löfstedt
series ordinal
1
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Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
Erik Onelöv
series ordinal
3
1 reference
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Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
Marie Meeths
series ordinal
5
1 reference
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Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
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3 March 2020
language of work or name
English
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publication date
3 December 2015
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Europe PubMed Central
PubMed publication ID
26686408
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retrieved
3 March 2020
published in
The Lancet. Haematology.
1 reference
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Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
volume
2
1 reference
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Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
issue
12
1 reference
stated in
Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
page(s)
e536-42
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Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
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Cancer epidemiology in the last century and the next decade
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Efficacy of MRI and mammography for breast-cancer screening in women with a familial or genetic predisposition
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Are antibody deficiency disorders associated with a narrower range of cancers than other forms of immunodeficiency?
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Perforinopathy: a spectrum of human immune disease caused by defective perforin delivery or function.
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7 January 2021
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Molecular mechanisms of biogenesis and exocytosis of cytotoxic granules
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7 January 2021
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Perforin-mediated cytotoxicity is critical for surveillance of spontaneous lymphoma
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7 January 2021
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Monoallelic mutations of the perforin gene may represent a predisposing factor to childhood anaplastic large cell lymphoma.
1 reference
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7 January 2021
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Temperature sensitivity of human perforin mutants unmasks subtotal loss of cytotoxicity, delayed FHL, and a predisposition to cancer
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7 January 2021
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A proportion of patients with lymphoma may harbor mutations of the perforin gene.
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Development of classical Hodgkin's lymphoma in an adult with biallelic STXBP2 mutations
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Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies
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Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5).
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Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D
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Incidence in Sweden and clinical features of familial hemophagocytic lymphohistiocytosis
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Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production
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7 January 2021
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Human perforin mutations and susceptibility to multiple primary cancers
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Perforin polymorphism A91V and susceptibility to B-precursor childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group
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Malignancies in the setting of primary immunodeficiency: Implications for hematologists/oncologists
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Papillomaviruses in the causation of human cancers - a brief historical account
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Identifiers
DOI
10.1016/S2352-3026(15)00223-9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
PubMed publication ID
26686408
1 reference
stated in
Europe PubMed Central
PubMed publication ID
26686408
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26686408%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 March 2020
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