Blood Protein Disorders research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Blood Protein Disorders 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 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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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
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
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
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
Research
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia.
Draptchinskaia N, Gustavsson P, Andersson B, Pettersson M, Willig T N ...
Nature genetics Vol 21(2)
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Date 01 Feb 1999
Research
Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia.
Noetzli Leila, Lo Richard W, Lee-Sherick Alisa B, Callaghan Michael, Noris Patrizia ...
Nature genetics Vol 47(5)
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Date 01 May 2015
Research
Mutations in SBDS are associated with Shwachman-Diamond syndrome.
Boocock Graeme R B, Morrison Jodi A, Popovic Maja, Richards Nicole, Ellis Lynda ...
Nature genetics Vol 33(1)
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Date 01 Jan 2003
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