Experiment Flashcards

1
Q

Why have you used this mice lineage ?

A

This lineage has been used in previous experiment from the research group in which they used the loxP –STOP-loxP-TdTomato construct in mouse genome to inject a transynaptic AAV within cortical area to label n+1 neurons and map them within the lumbar spinal cord.

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2
Q

13- Pro/Cons of the Quint Ebrain workflow

A

a. Pros: Semi-automated, gain of time during alignment, produce a 3D model and coordinate for each object which can be used for deeper analysis
b. Con: Requires more Random Access Memory, better PC, Pretty recent tool, Fiber segmentation takes time

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3
Q

What alternative we had to the Quint Ebrain workflow

A

a. Brain J, never managed to make it work. Fluorescence measurement but we preferred to observe the whole brain, without having to follow a pipeline for each brain section.

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4
Q

In which PD subtype is there a CST impairment ?

A

Multiple system atrophy parkinsonian variant.

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5
Q

What are the two mains impairments of CST in MSA PD ?

A

Reducted fractional anisotropy
Reduced central motor conduction time.

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6
Q

Cite three means to measure CST impairement involvment in humans ?

A

Diffusion tensor imaging
Transcranial magnetic stimulation and triple transcranial magnetic stimulation.

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7
Q

In mice, when does CST reaches the BS ?

A

At E17.

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8
Q

In mice, when does CST reaches the caudal medulla ?

A

E19.

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9
Q

In mice, when does CST cross the midline ?

A

P0

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10
Q

In mice, when does CST reaches the cervical segments ?

A

P2

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11
Q

In mice, when does CST reaches the thoracis segments ?

A

P5

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12
Q

In mice, when does CST reaches lumbar segments ?

A

P9

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13
Q

Cite three mains gene involved in CST specialisation.

A

Ctip2
Fezf2 (so they are not ending in cortical area)
Sox5 (synapse guidance and formation and growth)

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14
Q

marker for sensorimotor areas

A

BHLHB5 motor area

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15
Q

Important factor for CST growth

A

SEMA3A/C, SEMA6A
Netrin1
Pax6
Robo1/robo2
wnt, EPHA4

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16
Q

EG of disease in which there is an abnormal guidance

A

Congenital mirror movement
Klippelfeil syndrome (pyr decuss), walker syndrome