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1. Improving laboratory animal genetic reporting: LAG-R guidelines.

3. Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines

6. A resource of targeted mutant mouse lines for 5,061 genes

9. High-throughput discovery of novel developmental phenotypes

10. Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss

11. Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis via actomyosin dynamics deregulations

14. The Rogdi Knockout Mouse is a Model for Kohlschütter–Tönz Syndrome

17. The mammalian gene function resource: the International Knockout Mouse Consortium.

19. Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders

21. Changes in social behaviour with alterations of MAPK3 and KCTD13/CUL3 pathways in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders

26. TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis

27. IL-3 produced by T cells is crucial for basophil extravasation in hapten-induced allergic contact dermatitis.

28. Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models

29. AUTS2 gene dosage affects synaptic AMPA receptors via a local dendritic spine AUTS2-TTC3-AKT-mTORC1 signaling dysfunction

30. Ts66Yah, a mouse model of Down syndrome with improved construct and face validity

31. Keratinocyte-derived cytokine TSLP promotes growth and metastasis of melanoma by regulating the tumor-associated immune microenvironment

34. Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders.

36. Ts66Yah, an upgraded Ts65Dn mouse model for Down syndrome, for only the region homologous to Human chromosome 21

38. A conditional null allele of Dync1h1 enables targeted analyses of dynein roles in neuronal length sensing.

39. Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

44. Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder

45. PHENOMIN, your French partner for understanding mammalian gene function in mouse disease models: WS.001

46. Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration

47. Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome

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