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Jana Henck
Jana Henck
Max Planck Institute for molecular Genetics in Berlin
在 molgen.mpg.de 的电子邮件经过验证
标题
引用次数
引用次数
年份
Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state
S Smajić, CA Prada-Medina, Z Landoulsi, J Ghelfi, S Delcambre, ...
Brain 145 (3), 964-978, 2022
2382022
The histone methyltransferase DOT1L is required for proper DNA damage response, DNA repair, and modulates chemotherapy responsiveness
V Kari, SK Raul, JM Henck, J Kitz, F Kramer, RL Kosinsky, N Übelmesser, ...
Clinical epigenetics 11 (1), 1-13, 2019
512019
Single-cell sequencing of the human midbrain reveals glial activation and a neuronal state specific to Parkinson's disease
S Smajic, CA Prada-Medina, Z Landoulsi, C Dietrich, J Jarazo, J Henck, ...
medRxiv (The Preprint Server for health sciences.), 2020
192020
Single-cell RNA-based phenotyping reveals a pivotal role of thyroid hormone receptor alpha for hypothalamic development
VKA Sreenivasan, R Dore, J Resch, J Maier, C Dietrich, J Henck, ...
Development 150 (3), dev201228, 2023
72023
Single-cell, whole-embryo phenotyping of mammalian developmental disorders
X Huang, J Henck, C Qiu, VKA Sreenivasan, S Balachandran, OV Amarie, ...
Nature 623 (7988), 772-781, 2023
62023
Single cell, whole embryo phenotyping of pleiotropic disorders of mammalian development
X Huang, J Henck, C Qiu, VKA Sreenivasan, S Balachandran, R Behncke, ...
bioRxiv, 2022.08. 03.500325, 2022
42022
Single-cell sequencing: promises and challenges for human genetics
VKA Sreenivasan, J Henck, M Spielmann
Medizinische Genetik 34 (4), 261-273, 2022
12022
Structural Variants at the LMNB1 Locus: Deciphering Pathomechanisms in Autosomal Dominant Adult‐Onset Demyelinating Leukodystrophy
P Dimartino, M Zadorozhna, V Yumiceba, A Basile, I Cani, US Melo, ...
Annals of neurology, 2024
2024
Single-cell RNA phenotyping of a mouse model for hypothyroidism reveals a pivotal role of thyroid hormone receptor alpha for hypothalamic development
V Sreenivasan, R Dore, J Resch, J Maier, C Dietrich, J Henck, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 622-622, 2024
2024
Single cell, whole embryo phenotyping of pleiotropic disorders of mammalian development
J Henck, X Huang, C Qiu, V Sreenivasan, S Ulferts, R Behncke, ...
2023
Single cell sequencing as a phenotyping strategy to decipher the molecular mechanisms of developmental disorders
J Henck
2023
Single-cell characterization of patient midbrain tissue reveals tissue remodeling and glial activation in Parkinson's disease
S Smajic, C Prada-Medina, Z Landoulsi, J Ghelfi, S Delcambre, C Dietrich, ...
MOVEMENT DISORDERS 37, S595-S595, 2022
2022
Transcriptional single-cell atlas of human limb malformation candidate genes
CA Prada-Medina, G Cova, J Glaser, C Dietrich, J Henck, S Mundlos, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 133-133, 2020
2020
The Cdkl5 phenotype at single cell resolution
J Henck, C Prada, Y Herault, C Dietrich, V Suckow, VM Kalscheuer, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 381-381, 2020
2020
The histone methyltransferase DOT1L is required for proper DNA damage response, DNA repair, and modulates chemotherapy responsiveness
K Vijayalakshmi, SK Raul, JM Henck, J Kitz, F Kramer, RL Kosinsky, ...
Clinical Epigenetics 11, 2019
2019
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