 Connection
Lee Niswander to Humans
This is a "connection" page, showing publications Lee Niswander has written about Humans.
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Connection Strength |
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0.240 |
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Engelhardt DM, Martyr CA, Niswander L. Pathogenesis of neural tube defects: The regulation and disruption of cellular processes underlying neural tube closure. WIREs Mech Dis. 2022 09; 14(5):e1559.
Score: 0.022
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Kakebeen AD, Niswander L. Micronutrient imbalance and common phenotypes in neural tube defects. Genesis. 2021 11; 59(11):e23455.
Score: 0.021
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Brown HM, Murray SA, Northrup H, Au KS, Niswander LA. Snx3 is important for mammalian neural tube closure via its role in canonical and non-canonical WNT signaling. Development. 2020 11 19; 147(22).
Score: 0.020
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Li H, Niswander L. Does DNA methylation provide a link between folate and neural tube closure? Epigenomics. 2018 10; 10(10):1263-1265.
Score: 0.017
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Li H, Zhang J, Chen S, Wang F, Zhang T, Niswander L. Genetic contribution of retinoid-related genes to neural tube defects. Hum Mutat. 2018 04; 39(4):550-562.
Score: 0.017
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Wilde JJ, Siegenthaler JA, Dent SY, Niswander LA. Diencephalic Size Is Restricted by a Novel Interplay Between GCN5 Acetyltransferase Activity and Retinoic Acid Signaling. J Neurosci. 2017 03 08; 37(10):2565-2579.
Score: 0.015
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Hanson MG, Wilde JJ, Moreno RL, Minic AD, Niswander L. Potassium dependent rescue of a myopathy with core-like structures in mouse. Elife. 2015 Jan 07; 4.
Score: 0.013
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Hanson MG, Fregoso VL, Vrana JD, Tucker CL, Niswander LA. Peripheral nervous system defects in a mouse model for peroxisomal biogenesis disorders. Dev Biol. 2014 Nov 01; 395(1):84-95.
Score: 0.013
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Schnatwinkel C, Niswander L. Nubp1 is required for lung branching morphogenesis and distal progenitor cell survival in mice. PLoS One. 2012; 7(9):e44871.
Score: 0.011
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Ray HJ, Niswander L. Mechanisms of tissue fusion during development. Development. 2012 May; 139(10):1701-11.
Score: 0.011
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Marean A, Graf A, Zhang Y, Niswander L. Folic acid supplementation can adversely affect murine neural tube closure and embryonic survival. Hum Mol Genet. 2011 Sep 15; 20(18):3678-83.
Score: 0.010
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Zohn IE, Anderson KV, Niswander L. Using genomewide mutagenesis screens to identify the genes required for neural tube closure in the mouse. Birth Defects Res A Clin Mol Teratol. 2005 Sep; 73(9):583-90.
Score: 0.007
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Zohn IE, Chesnutt CR, Niswander L. Cell polarity pathways converge and extend to regulate neural tube closure. Trends Cell Biol. 2003 Sep; 13(9):451-4.
Score: 0.006
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Terhune EA, Cuevas MT, Monley AM, Wethey CI, Chen X, Cattell MV, Bayrak MN, Bland MR, Sutphin B, Trahan GD, Taylor MRG, Niswander LA, Jones KL, Baschal EE, Antunes L, Dobbs M, Gurnett C, Appel B, Gray R, Hadley Miller N. Mutations in KIF7 implicated in idiopathic scoliosis in humans and axial curvatures in zebrafish. Hum Mutat. 2021 04; 42(4):392-407.
Score: 0.005
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Zou J, Wang F, Yang X, Wang H, Niswander L, Zhang T, Li H. Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes. Neural Dev. 2020 07 10; 15(1):8.
Score: 0.005
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Li H, Wang X, Zhao H, Wang F, Bao Y, Guo J, Chang S, Wu L, Cheng H, Chen S, Zou J, Cui X, Niswander L, Finnell RH, Wang H, Zhang T. Low folate concentration impacts mismatch repair deficiency in neural tube defects. Epigenomics. 2020 01; 12(1):5-18.
Score: 0.005
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Niswander L. Developmental biology. Legs to wings and back again. Nature. 1999 Apr 29; 398(6730):751-2.
Score: 0.005
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Baschal EE, Terhune EA, Wethey CI, Baschal RM, Robinson KD, Cuevas MT, Pradhan S, Sutphin BS, Taylor MRG, Gowan K, Pearson CG, Niswander LA, Jones KL, Miller NH. Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology. G3 (Bethesda). 2018 07 31; 8(8):2663-2672.
Score: 0.004
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Van Otterloo E, Feng W, Jones KL, Hynes NE, Clouthier DE, Niswander L, Williams T. MEMO1 drives cranial endochondral ossification and palatogenesis. Dev Biol. 2016 07 15; 415(2):278-295.
Score: 0.004
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Niswander L, Jeffrey S, Martin GR, Tickle C. A positive feedback loop coordinates growth and patterning in the vertebrate limb. Nature. 1994 Oct 13; 371(6498):609-12.
Score: 0.003
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Apkon SD, Grady R, Hart S, Lee A, McNalley T, Niswander L, Petersen J, Remley S, Rotenstein D, Shurtleff H, Warner M, Walker WO. Advances in the care of children with spina bifida. Adv Pediatr. 2014 Aug; 61(1):33-74.
Score: 0.003
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Feng W, Choi I, Clouthier DE, Niswander L, Williams T. The Ptch1(DL) mouse: a new model to study lambdoid craniosynostosis and basal cell nevus syndrome-associated skeletal defects. Genesis. 2013 Oct; 51(10):677-89.
Score: 0.003
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Parker JJ, Dionne KR, Massarwa R, Klaassen M, Foreman NK, Niswander L, Canoll P, Kleinschmidt-Demasters BK, Waziri A. Gefitinib selectively inhibits tumor cell migration in EGFR-amplified human glioblastoma. Neuro Oncol. 2013 Aug; 15(8):1048-57.
Score: 0.003
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Wallingford JB, Niswander LA, Shaw GM, Finnell RH. The continuing challenge of understanding, preventing, and treating neural tube defects. Science. 2013 Mar 01; 339(6123):1222002.
Score: 0.003
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Becker-Heck A, Zohn IE, Okabe N, Pollock A, Lenhart KB, Sullivan-Brown J, McSheene J, Loges NT, Olbrich H, Haeffner K, Fliegauf M, Horvath J, Reinhardt R, Nielsen KG, Marthin JK, Baktai G, Anderson KV, Geisler R, Niswander L, Omran H, Burdine RD. The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation. Nat Genet. 2011 Jan; 43(1):79-84.
Score: 0.003
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Weatherbee SD, Niswander LA, Anderson KV. A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling. Hum Mol Genet. 2009 Dec 01; 18(23):4565-75.
Score: 0.002
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Zohn IE, De Domenico I, Pollock A, Ward DM, Goodman JF, Liang X, Sanchez AJ, Niswander L, Kaplan J. The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin disease. Blood. 2007 May 15; 109(10):4174-80.
Score: 0.002
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Niemann S, Zhao C, Pascu F, Stahl U, Aulepp U, Niswander L, Weber JL, M?ller U. Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family. Am J Hum Genet. 2004 Mar; 74(3):558-63.
Score: 0.002
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Liu A, Li JY, Bromleigh C, Lao Z, Niswander LA, Joyner AL. FGF17b and FGF18 have different midbrain regulatory properties from FGF8b or activated FGF receptors. Development. 2003 Dec; 130(25):6175-85.
Score: 0.002
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Varley JE, McPherson CE, Zou H, Niswander L, Maxwell GD. Expression of a constitutively active type I BMP receptor using a retroviral vector promotes the development of adrenergic cells in neural crest cultures. Dev Biol. 1998 Apr 01; 196(1):107-18.
Score: 0.001
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Davidson JN, Rao GN, Niswander L, Andreano C, Tamer C, Chen KC. Organization and nucleotide sequence of the 3' end of the human CAD gene. DNA Cell Biol. 1990 Nov; 9(9):667-76.
Score: 0.001
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Connection Strength
The connection strength for concepts is the sum of the scores for each matching publication.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
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