Leukopenia research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Leukopenia treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 19 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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5213 Abstracts
Research
Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis.
Khajuria Rajiv K, Munschauer Mathias, Ulirsch Jacob C, Fiorini Claudia, Ludwig Leif S ...
Cell Vol 173(1)
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Date 22 Mar 2018
Research
Crosstalk between sentinel and helper macrophages permits neutrophil migration into infected uroepithelium.
Schiwon Marzena, Weisheit Christina, Franken Lars, Gutweiler Sebastian, Dixit Akanksha ...
Cell Vol 156(3)
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Date 30 Jan 2014
Research
Increased myeloid cell responses to M-CSF and RANKL cause bone loss and inflammation in SH3BP2 "cherubism" mice.
Ueki Yasuyoshi, Lin Chin-Yu, Senoo Makoto, Ebihara Takeshi, Agata Naoki ...
Cell Vol 128(1)
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Date 12 Jan 2007
Research
Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.
Ho M, Chelly J, Carter N, Danek A, Crocker P ...
Cell Vol 77(6)
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Date 17 Jun 1994
Research
A common missense variant in NUDT15 confers susceptibility to thiopurine-induced leukopenia.
Yang Suk-Kyun, Hong Myunghee, Baek Jiwon, Choi Hyunchul, Zhao Wanting ...
Nature genetics Vol 46(9)
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Date 01 Sep 2014
Research
Physiogenomic resources for rat models of heart, lung and blood disorders.
Malek Renae L, Wang Hong-ying, Kwitek Anne E, Greene Andrew S, Bhagabati Nirmal ...
Nature genetics Vol 38(2)
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Date 01 Feb 2006
Research
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.
Iotchkova Valentina, Huang Jie, Morris John A, Jain Deepti, Barbieri Caterina ...
Nature genetics Vol 48(11)
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Date 01 Nov 2016
Research
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia.
Guernsey Duane L, Jiang Haiyan, Campagna Dean R, Evans Susan C, Ferguson Meghan ...
Nature genetics Vol 41(6)
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Date 01 Jun 2009
Research
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome.
Diaz G A, Banikazemi M, Oishi K, Desnick R J, Gelb B D
Nature genetics Vol 22(3)
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Date 01 Jul 1999
Research
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Kamatani Yoichiro, Matsuda Koichi, Okada Yukinori, Kubo Michiaki, Hosono Naoya ...
Nature genetics Vol 42(3)
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Date 01 Mar 2010
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