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piecemeal microautophagy of nucleus

Known as: PMN 
Degradation of a cell nucleus by lysosomal microautophagy. [GOC:jp, PMID:18701704]
National Institutes of Health

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Highly Cited
2013
Highly Cited
2013
Two major populations of myeloid-derived suppressor cells (MDSCs), monocytic MDSCs (M-MDSCs) and polymorphonuclear MDSCs (PMN… Expand
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Highly Cited
2005
Highly Cited
2005
In the developing spinal cord, early progenitor cells of the oligodendrocyte lineage are induced in the motor neuron progenitor… Expand
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Highly Cited
2005
Highly Cited
2005
Spinal motor neurons and oligodendrocytes are generated sequentially from a common pool of progenitors termed pMN cells. Olig2 is… Expand
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Highly Cited
2003
Highly Cited
2003
Apoptosis is a hallmark of motoneuron diseases such as amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA) [1… Expand
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Highly Cited
2002
Highly Cited
2002
OLIG1 and OLIG2 are basic-helix-loop-helix (bHLH) transcription factors expressed in the pMN domain of the spinal cord, which… Expand
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Highly Cited
2001
Highly Cited
2001
Salinity has been suggested as being a controlling factor for blooms of N2-fixing cyanobacteria in estuaries. We tested the… Expand
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Highly Cited
1997
Highly Cited
1997
Motor neuron diseases such as amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy cause progressive paralysis, often… Expand
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Highly Cited
1995
Highly Cited
1995
Bcl-2 and its analogs protect different classes of neurons from apoptosis in several experimental situations. These proteins may… Expand
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Highly Cited
1992
Highly Cited
1992
CILIARY neurotrophic factor (CNTF) supports the survival of embryonic motor neurons in vitro1,2 and in vivo3, and prevents lesion… Expand
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Highly Cited
1991
Highly Cited
1991
A new autosomal-recessive mouse mutant with progressive motor neuronopathy (pmn) is described. Homozygotes develop paralysis of… Expand
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