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Closing the Care Gap with Wearable Devices: Innovating Healthcare with Wearable Patient Monitoring

1, 2022

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Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita

American journal of human genetics, 2013-03, Vol.92 (3), p.448-453

2013

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Differences in disease severity but similar telomere lengths in genetic subgroups of patients with telomerase and shelterin mutations

PloS one, 2011-09, Vol.6 (9), p.e24383-e24383

2011

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Mimetic Theory and Islam: "The Wound Where Light Enters"

Michael Kirwan, Ahmad Achtar

1, 2019

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Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita

Proceedings of the National Academy of Sciences - PNAS, 2008-06, Vol.105 (23), p.8073-8078

2008

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The Drama of the World, the Drama of Theology

Religions (Basel, Switzerland ), 2022-11, Vol.13 (11), p.1093

Kirwan, Michael Joseph

2022

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'Faith without ideology is dead': what are the implications for Religious Education in Catholic schools and colleges of taking this assertion seriously? An essay for teachers of the subject to consider

International studies in Catholic education, 2021-07, Vol.ahead-of-print (ahead-of-print), p.1-14

2021

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Mutations in the telomere capping complex in bone marrow failure and related syndromes

Haematologica (Roma), 2013-03, Vol.98 (3), p.334-338

2013

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Adhesion of Streptococcus pneumoniae to human airway epithelial cells exposed to urban particulate matter

Journal of allergy and clinical immunology, 2011-05, Vol.127 (5), p.1236-1242.e2

2011

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ERCC6L2 Mutations Link a Distinct Bone-Marrow-Failure Syndrome to DNA Repair and Mitochondrial Function

American journal of human genetics, 2014-02, Vol.94 (2), p.246-256

2014

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Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome

Blood, 2007-12, Vol.110 (13), p.4198-4205

2007

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René Girard Among the Theologians

Logos (Moscow, Russia), 2024, Vol.34 (3), p.29-48

Kirwan, Michael

2024

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Validation of a child-friendly version of the monetary incentive delay task

Social cognitive and affective neuroscience, 2013-08, Vol.8 (6), p.720-726

2013

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Regulatory barriers blocking standardization of interoperability

JMIR mHealth and uHealth, 2013-07, Vol.1 (2), p.e13-e13

2013

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Surviving the Secular: Faith, Grief, Parody

Studies: An Irish Quarterly Review, 2022-10, Vol.111 (443), p.239-248

Kirwan, Michael

2022

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Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia

Human mutation, 2009-11, Vol.30 (11), p.1567-1573

2009

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

Haematologica (Roma), 2012-04, Vol.97 (4), p.524-528

2012

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Dyskeratosis congenita and the DNA damage response

British journal of haematology, 2011-06, Vol.153 (5), p.634-643

2011

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Dyskeratosis congenita, stem cells and telomeres

Biochimica et biophysica acta, 2009-04, Vol.1792 (4), p.371-379

2009

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"Beyond the Gates": René Girard and the Persistence of Sacrifice

Journal of continental philosophy (Online), 2021, Vol.2 (2), p.277-294

Kirwan, Michael

2021

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How do we define the “general purpose”?

Computer standards and interfaces, 2014-11, Vol.36 (6), p.963-965

2014

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Functional characterization of novel telomerase RNA (TERC) mutations in patients with diverse clinical and pathological presentations

Haematologica (Roma), 2007-08, Vol.92 (8), p.1013-1020

2007

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Dyskeratosis congenita: a genetic disorder of many faces

Clinical genetics, 2008-02, Vol.73 (2), p.103-112

2008

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TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes

Blood, 2008-11, Vol.112 (9), p.3594-3600

2008

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The Unbearable Humanum: Reflecting Back, Working Forwards

New Blackfriars, 2015-03, Vol.96 (1062), p.239-251

Kirwan SJ, Michael

2015

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Closing the Care Gap with Wearable Devices: Innovating Healthcare with Wearable Patient Monitoring

Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita

Differences in disease severity but similar telomere lengths in genetic subgroups of patients with telomerase and shelterin mutations

Mimetic Theory and Islam: "The Wound Where Light Enters"

Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita

The Drama of the World, the Drama of Theology

'Faith without ideology is dead': what are the implications for Religious Education in Catholic schools and colleges of taking this assertion seriously? An essay for teachers of the subject to consider

Mutations in the telomere capping complex in bone marrow failure and related syndromes

Adhesion of Streptococcus pneumoniae to human airway epithelial cells exposed to urban particulate matter

ERCC6L2 Mutations Link a Distinct Bone-Marrow-Failure Syndrome to DNA Repair and Mitochondrial Function

Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome

René Girard Among the Theologians

Validation of a child-friendly version of the monetary incentive delay task

Regulatory barriers blocking standardization of interoperability

Surviving the Secular: Faith, Grief, Parody

Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia

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

Dyskeratosis congenita and the DNA damage response

Dyskeratosis congenita, stem cells and telomeres

"Beyond the Gates": René Girard and the Persistence of Sacrifice

How do we define the “general purpose”?

Functional characterization of novel telomerase RNA (TERC) mutations in patients with diverse clinical and pathological presentations

Dyskeratosis congenita: a genetic disorder of many faces

TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes

The Unbearable Humanum: Reflecting Back, Working Forwards

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