|1.||Yu, Qin: 1 article (01/2012)|
|2.||Murray, Lucas B: 1 article (01/2012)|
|3.||Lau, Ying-Ka Ingar: 1 article (01/2012)|
|4.||Ahn, Hyo Seop: 1 article (10/2010)|
|5.||Seo, Jong Jin: 1 article (10/2010)|
|6.||Shin, Hee Young: 1 article (10/2010)|
|7.||Kang, Daehee: 1 article (10/2010)|
|8.||Lee, Kyoung-Mu: 1 article (10/2010)|
|9.||Kang, Hyoung Jin: 1 article (10/2010)|
|10.||Choi, Ji Eun: 1 article (10/2010)|
11/01/1991 - "Hereditary elliptocytosis due to both qualitative and quantitative defects in membrane skeletal protein 4.1."
01/01/1987 - "In homozygous 4.1 (-) hereditary elliptocytosis where the primary defect was presumably the absence of the membrane skeletal protein 4.1, there was approximatively a 70% reduction in the minor sialoglycoproteins beta and gamma. "
|3.||Precursor Cell Lymphoblastic Leukemia-Lymphoma (Acute Lymphoblastic Leukemia)
|4.||Neurofibromatosis 2 (Neurofibromatosis Type II)
04/01/2007 - "Both Mer and Ex are members of the Band 4.1 protein superfamily, and, based on analyses of mer ex double mutants, they are proposed to function together in at least a partially redundant manner upstream of the Hippo (Hpo) and Warts (Wts) proteins to regulate cell growth and division. "
|1.||Proteins (Proteins, Gene)
|2.||Neurofibromin 2 (Merlin)
|4.||Messenger RNA (mRNA)
|5.||neuronal membrane cytoskeletal protein 4.1