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S

Soeren S. Lienkamp

university of zurich
H指数:29
被引数:1.0万

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Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development
NATURE COMMUNICATIONS
IF15.7
2024-10-260
OAAI
Ceroni, Fabiola; Cicekdal, Munevver B.; Holt, Richard; Sorokina, Elena; Chassaing, Nicolas; Clokie, Samuel; Naert, Thomas; Talbot, Lidiya V.; Muheisen, Sanaa; Bax, Dorine A.; Kesim, Yesim; Kivuva, Emma C.; Vincent-Delorme, Catherine; Lienkamp, Soeren S.; Plaisancie, Julie; De Baere, Elfride; Calvas, Patrick; Vleminckx, Kris; Semina, Elena V.; Ragge, Nicola K.
Benchtop mesoSPIM: a next-generation open-source light-sheet microscope for cleared samples
NATURE COMMUNICATIONS
IF15.7
2024-03-275
OAAI
Vladimirov, Nikita; Voigt, Fabian F.; Naert, Thomas; Araujo, Gabriela R.; Cai, Ruiyao; Reuss, Anna Maria; Zhao, Shan; Schmid, Patricia; Hildebrand, Sven; Schaettin, Martina; Groos, Dominik; Mateos, Jose Maria; Bethge, Philipp; Yamamoto, Taiyo; Aerne, Valentino; Roebroeck, Alard; Ertuerk, Ali; Aguzzi, Adriano; Ziegler, Urs; Stoeckli, Esther; Baudis, Laura; Lienkamp, Soeren S.; Helmchen, Fritjof
Specific disruption of calcineurin-signaling in the distal convoluted tubule impacts the transcriptome and proteome, and causes hypomagnesemia and metabolic acidosis

远曲小管中钙调神经磷酸酶信号的特异性破坏会影响转录组和蛋白质组，并导致低镁血症和代谢性酸中毒

KIDNEY INTERNATIONAL
IF12.6
2021-10-0120
OAAI
Banki, Eszter; Fisi, Viktoria; Moser, Sandra; Wengi, Agnieszka; Carrel, Monique; Loffing-Cueni, Dominique; Penton, David; V. Kratschmar, Denise; Rizzo, Ludovica; Lienkamp, Soeren; Odermatt, Alex; Rinschen, Markus M.; Loffing, Johannes
Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease

Ttc30a影响多囊肾疾病睫状软骨发育不良模型中的微管蛋白修饰

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
IF9.1
2021-09-219
OAAI
Getwan, Maike; Hoppmann, Anselm; Schlosser, Pascal; Grand, Kelli; Song, Weiting; Diehl, Rebecca; Schroda, Sophie; Heeg, Florian; Deutsch, Konstantin; Hildebrandt, Friedhelm; Lausch, Ekkehart; Kottgen, Anna; Lienkamp, Soeren S.
Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome

CBY1的丢失导致以Joubert综合征为特征的纤毛病

HUMAN MUTATION
IF3.7
2020-11-0117
OAAI
Epting, Daniel; Senaratne, Lokuliyange D. S.; Ott, Elisabeth; Holmgren, Asbjorn; Sumathipala, Dulika; Larsen, Selma M.; Wallmeier, Julia; Bracht, Diana; Frikstad, Kari-Anne M.; Crowley, Suzanne; Sikiric, Alma; Baroy, Tuva; Kasmann-Kellner, Barbara; Decker, Eva; Decker, Christian; Bachmann, Nadine; Patzke, Sebastian; Phelps, Ian G.; Katsanis, Nicholas; Giles, Rachel; Schmidts, Miriam; Zucknick, Manuela; Lienkamp, Soeren S.; Omran, Heymut; Davis, Erica E.; Doherty, Dan; Stromme, Petter; Frengen, Eirik; Bergmann, Carsten; Misceo, Doriana

研究方向

暂未获取到该数据
G
Gerd Walz
H 指数:76论文数:596被引数:2.2万
R
Roman Pichler
H 指数:10论文数:17被引数:356
S
Sylvia Hoff
H 指数:10论文数:23被引数:643
M
Michael M. Kaminski
H 指数:16论文数:39被引数:2,222
A
Albrecht Kramer-Zucker
H 指数:28论文数:41被引数:4,419
F
Friedhelm Hildebrandt
H 指数:108论文数:592被引数:3.7万
D
Daniel Epting
H 指数:14论文数:34被引数:918
K
Kelli Grand
H 指数:7论文数:14被引数:224
O
Olaf Ronneberger
H 指数:52论文数:154被引数:17.1万
H
Heymut Omran
H 指数:88论文数:412被引数:2.6万