Suchergebnisse - "Hahn, Michael"

PubPharm (902)

61

Defective X-gating caused byde novogain-of-function mutations inKCNK3underlies a developmental disorder with sleep apnea

enthalten in: bioRxiv.org | 2023

von Sörmann, J. | Schewe, M. | Proks, P. | +27

62

Botrytis cinerea infection accelerates ripening and cell wall disassembly to promote disease in tomato fruit

enthalten in: Plant physiology | 2023

von Silva, C. | Adaskaveg, J. | Mesquida-Pesci, S. | +8

63

Modeling task effects in human reading with neural network-based attention

enthalten in: Cognition | 2023

von Hahn, M. | Keller, F.

64

ReIGNITE RT Boost: An international study testing the accuracy and feasibility of using restriction spectrum imaging (RSI) MRI to guide intraprostatic tumor target volume for radiotherapy boost

enthalten in: bioRxiv.org | 2022

von Lui, A. | Kallis, K. | Zhong, A. | +13

65

A unifying theory explains seemingly contradicting biases in perceptual estimation

enthalten in: bioRxiv.org | 2022

von Hahn, M. | Wei, X.

66

Deriving instrumental point spread functions from partially occulted images

enthalten in: Journal of the Optical Society of America. A, Optics, image science, and vision | 2022

von Hofmeister, S. | Hahn, M. | Wolf Savin, D.

67

Botrytis cinerea infection accelerates ripening and cell wall disassembly to promote disease in tomato fruit

enthalten in: bioRxiv.org | 2022

von Silva, C. | Adaskaveg, J. | Mesquida-Pesci, S. | +8

68

An evolutionary conserved division-of-labor between hippocampal and neocortical sharp-wave ripples organizes information transfer during sleep

enthalten in: bioRxiv.org | 2022

von van Schalkwijk, F. | Weber, J. | Hahn, M. | +4

69

A resource-rational model of human processing of recursive linguistic structure

enthalten in: Proceedings of the National Academy of Sciences of the United States of America | 2022

von Hahn, M. | Futrell, R. | Levy, R. | +1

CommentIn: Proc Natl Acad Sci U S A. 2022 Dec 6;119(49):e2217108119. - PMID 36449546

70

Gain-of-function mutations in KCNK3 cause a developmental disorder with sleep apnea

enthalten in: Nature genetics | 2022

von Sörmann, J. | Schewe, M. | Proks, P. | +27

CommentIn: Nat Genet. 2022 Oct;54(10):1451-1452. - PMID 36195756