Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms.
about
Myeloid neoplasms with germline DDX41 mutation.Ataxia-pancytopenia syndrome with SAMD9L mutations.Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome.New monogenic disorders identify more pathways to neutropenia: from the clinic to next-generation sequencing.The genomic landscape of pediatric myelodysplastic syndromes.Cord blood NK cells engineered to express IL-15 and a CD19-targeted CAR show long-term persistence and potent antitumor activity.A paralogous pair of mammalian host restriction factors form a critical host barrier against poxvirus infection.Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7.SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies.Germline SAMD9 and SAMD9L mutations are associated with extensive genetic evolution and diverse hematologic outcomesNetwork analysis of inflammatory responses to sepsis by neutrophils and peripheral blood mononuclear cells
P2860
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P2860
Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Gain-of-function SAMD9L mutati ...... DS, and neurological symptoms.
@en
type
label
Gain-of-function SAMD9L mutati ...... DS, and neurological symptoms.
@en
prefLabel
Gain-of-function SAMD9L mutati ...... DS, and neurological symptoms.
@en
P2093
P2860
P50
P1433
P1476
Gain-of-function SAMD9L mutati ...... DS, and neurological symptoms.
@en
P2093
Alexandra Rundberg Nilsson
Andreas Puschmann
Cornelis Jan Pronk
Hannaleena Kokkonen
Johanna Uusimaa
Jonna Komulainen-Ebrahim
Josef Davidsson
Jörg Cammenga
Lars Nilsson
Matthias Voss
P2860
P304
P356
10.1182/BLOOD-2016-10-743302
P407
P50
P577
2017-02-15T00:00:00Z