André Hanauer - Publications, H-index & Citations

André Hanauer

institut national de la sante et de la recherche medicale (inserm)

39H指数

131论文数

8.1K被引数

收录论文 30

发表时间

Fibroblast Growth Factor Receptor 3 Associates with and Tyrosine Phosphorylates p90 RSK2, Leading to RSK2 Activation That Mediates Hematopoietic Transformation

MOLECULAR AND CELLULAR BIOLOGY

IF2.7

2023-03-21

OAAI

Kang, Sumin; Elf, Shannon; Dong, Shaozhong; Hitosugi, Taro; Lythgoe, Katherine; Guo, Ailan; Ruan, Hong; Lonial, Sagar; Khoury, Hanna J.; Williams, Ifor R.; Lee, Benjamin H.; Roesel, Johannes L.; Karsenty, Gerard; Hanauer, Andre; Taunton, Jack; Boggon, Titus J.; Gu, Ting-Lei; Chen, Jing

Structural and Functional Basis for p38-MK2-Activated Rsk Signaling in Toll-Like Receptor-Stimulated Dendritic Cells

MOLECULAR AND CELLULAR BIOLOGY

IF2.7

2023-03-20

OAAI

Zaru, Rossana; Edgar, Alexander J.; Hanauer, Andre; Watts, Colin

Selective alteration of adult hippocampal neurogenesis and impaired spatial pattern separation performance in the RSK2-deficient mouse model of Coffin-Lowry syndrome

NEUROBIOLOGY OF DISEASE

IF5.6

2018-07-01

PREAI

Castillon, Charlotte; Lunion, Steeve; Desvignes, Nathalie; Hanauer, Andre; Laroche, Serge; Poirier, Roseline

The PDK1-Rsk Signaling Pathway Controls Langerhans Cell Proliferation and Patterning

JOURNAL OF IMMUNOLOGY

IF3.4

2015-11-01

OAAI

Zaru, Rossana; Matthews, Stephen P.; Edgar, Alexander J.; Prescott, Alan R.; Gomez-Nicola, Diego; Hanauer, Andre; Watts, Colin

PLD1 participates in BDNF-induced signalling in cortical neurons

SCIENTIFIC REPORTS

IF3.9

2015-10-06

OAAI

Ammar, Mohamed Raafet; Thahouly, Tamou; Hanauer, Andre; Stegner, David; Nieswandt, Bernhard; Vitale, Nicolas

Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin-Lowry syndrome

NEUROBIOLOGY OF DISEASE

IF5.6

2013-10-01

PREAI

Morice, Elise; Farley, Severine; Poirier, Roseline; Dallerac, Glenn; Chagneau, Carine; Pannetier, Solange; Hanauer, Andre; Davis, Sabrina; Vaillend, Cyrille; Laroche, Serge

Anchored p90 Ribosomal S6 Kinase 3 Is Required for Cardiac Myocyte Hypertrophy

CIRCULATION RESEARCH

IF16.2

2013-01-04

OAAI

Li, Jinliang; Kritzer, Michael D.; Michel, Jennifer J. Carlisle; Le, Andrew; Thakur, Hrishikesh; Gayanilo, Marjorie; Passariello, Catherine L.; Negro, Alejandra; Danial, Joshua B.; Oskouei, Behzad; Sanders, Michael; Hare, Joshua M.; Hanauer, Andre; Dodge-Kafka, Kimberly; Kapiloff, Michael S.

RSK2 Signaling in Medial Habenula Contributes to Acute Morphine Analgesia 内侧缰核RSK2信号通路在吗啡急性镇痛中的作用

NEUROPSYCHOPHARMACOLOGY

IF7.1

2012-01-04

OAAI

Darcq, Emmanuel; Befort, Katia; Koebel, Pascale; Pannetier, Solange; Mahoney, Megan K.; Gaveriaux-Ruff, Claire; Hanauer, Andre; Kieffer, Brigitte L.

Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin-Lowry syndrome

HUMAN GENETICS

IF3.6

2010-11-30

PREAI

Mehmood, Tahir; Schneider, Anne; Sibillec, Jeremie; Pereira, Patricia Marques; Pannetier, Solange; Ammar, Mohamed Raafet; Dembele, Doulaye; Thibault-Carpentier, Christelle; Rouach, Nathalie; Hanauer, Andre

Coffin-Lowry syndrome

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2009-11-04

119

OAAI

Pereira, Patricia Marques; Schneider, Anne; Pannetier, Solange; Heron, Delphine; Hanauer, Andre

The Coffin-Lowry syndrome-associated protein RSK2 is implicated in calcium-regulated exocytosis through the regulation of PLD1

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2008-06-17

OAAI

Zeniou-Meyer, Maria; Liu, Yuanyuan; Begle, Aurelie; Olanish, Mary; Hanauer, Andre; Becherer, Ute; Rettig, Jens; Bader, Marie-France; Vitale, Nicolas

The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient

HUMAN GENETICS

IF3.6

2007-08-24

PREAI

Pereira, Patricia Marques; Heron, Delphine; Hanauer, Andre

Deletion of the Coffin-Lowry syndrome gene RSK2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior

BEHAVIOR GENETICS

IF2.2

2006-10-11

PREAI

Poirier, R.; Jacquot, S.; Vaillend, C.; Soutthiphong, A. A.; Libbey, M.; Davis, S.; Laroche, S.; Hanauer, A.; Welzl, H.; Lipp, H. -P.; Wolfer, D. P.

Genetic background of HSH in three Polish families and a patient with an X;9 translocation

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2005-11-02

OAAI

Jalkanen, R; Pronicka, E; Tyynismaa, H; Hanauer, A; Walder, R; Alitalo, T

Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation

HUMAN GENETICS

IF3.6

2005-10-26

PREAI

Hagens, O; Dubos, A; Abidi, F; Barbi, G; Van Zutven, L; Hoeltzenbein, M; Tommerup, N; Moraine, C; Fryns, JP; Chelly, J; van Bokhoven, H; Gécz, J; Dollfus, HN; Ropers, HH; Schwartz, CE; dos Santos, RCS; Kalscheuer, V; Hanauer, A

p90Rsk is not involved in cytostatic factor arrest in mouse oocytes

JOURNAL OF CELL BIOLOGY

IF6.4

2005-04-18

OAAI

Dumont, J; Umbhauer, M; Rassinier, P; Hanauer, A; Verlhac, MH

Unusual splice-site mutations in the RSK2 gene and suggestion of genetic heterogeneity in Coffin-Lowry syndrome

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2002-06-01

OAAI

Zeniou, M; Pannetier, S; Fryns, JP; Hanauer, A