화학공학소재연구정보센터
검색결과 : 8건
No. Article
1 The mole genome reveals regulatory rearrangements associated with adaptive intersexuality
Real FM, Haas SA, Franchini P, Xiong P, Simakov O, Kuhl H, Schopflin R, Heller D, Moeinzadeh MH, Heinrich V, Krannich T, Bressin A, Hartmann MF, Wudy SA, Dechmann DKN, Hurtado A, Barrionuevo FJ, Schindler M, Harabula I, Osterwalder M, Hiller M, Wittler L, Visel A, Timmermann B, Meyer A, Vingron M, Jimenez R, Mundlos S, Lupianez DG
Science, 370(6513), 208, 2020
2 The single-cell transcriptional landscape of mammalian organogenesis
Cao JY, Spielmann M, Qiu XJ, Huang XF, Ibrahim DM, Hill AJ, Zhang F, Mundlos S, Christiansen L, Steemers FJ, Trapnell C, Shendure J
Nature, 566(7745), 496, 2019
3 Formation of new chromatin domains determines pathogenicity of genomic duplications
Franke M, Ibrahim DM, Andrey G, Schwarzer W, Heinrich V, Schopflin R, Kraft K, Kempfer R, Jerkovic I, Chan WL, Spielmann M, Timmermann B, Wittler L, Kurth I, Cambiaso P, Zuffardi O, Houge G, Lambie L, Brancati F, Pombo A, Vingron M, Spitz F, Mundlos S
Nature, 538(7624), 265, 2016
4 The organization of the osteocyte network mirrors the extracellular matrix orientation in bone
Kerschnitzki M, Wagermaier W, Roschger P, Seto J, Shahar R, Duda GN, Mundlos S, Fratzl P
Journal of Structural Biology, 173(2), 303, 2011
5 Fetal and postnatal mouse bone tissue contains more calcium than is present in hydroxyapatite
Lange C, Li C, Manjubala I, Wagermaier W, Kuhnisch J, Kolanczyk M, Mundlos S, Knaus P, Fratzl P
Journal of Structural Biology, 176(2), 159, 2011
6 The LIM domain protein Wtip interacts with the receptor tyrosine kinase Ror2 and inhibits canonical Wnt signalling
van Wijk NV, Witte F, Feike AC, Schambony A, Birchmeier W, Mundlos S, Stricker S
Biochemical and Biophysical Research Communications, 390(2), 211, 2009
7 Polyalanine Expansion in Synpolydactyly Might Result from Unequal Crossing-over of Hoxd13 - Response
Muragaki Y, Mundlos S, Upton J, Olsen BR
Science, 275(5298), 409, 1997
8 Altered Growth and Branching Patterns in Synpolydactyly Caused by Mutations in Hoxd13
Muragaki Y, Mundlos S, Upton J, Olsen BR
Science, 272(5261), 548, 1996