FAQ

Partial Wave Spectroscopic Microscopy

Known as: PWS 
A technique that uses focused waves of broadband, low-spatially-coherent light to illuminate a sample, and forms an image by acquiring far field back… (More)

Topic mentions per year

Topic mentions per year

1969-2017
05010019692017

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Label-free imaging of the native, living cellular nanoarchitecture using partial-wave spectroscopic microscopy.
The organization of chromatin is a regulator of molecular processes including transcription, replication, and DNA repair. The… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2010
Highly Cited
2010
Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome
Prader–Willi syndrome (PWS) is a neurobehavioral disorder manifested by infantile hypotonia and feeding difficulties in infancy… (More)
  • figure 2
  • figure 3
  • table 1
Is this relevant?
Highly Cited
2003
Highly Cited
2003
Serum ghrelin levels are inversely correlated with body mass index, age, and insulin concentrations in normal children and are markedly increased in Prader-Willi syndrome.
Ghrelin, an endogenous ligand of the GH secretagogue receptor, stimulates appetite and causes obesity in animal models and in… (More)
Is this relevant?
Highly Cited
2002
Highly Cited
2002
Elevated plasma ghrelin levels in Prader–Willi syndrome
 
  • figure 1
Is this relevant?
Highly Cited
2002
Highly Cited
2002
High circulating ghrelin: a potential cause for hyperphagia and obesity in prader-willi syndrome.
Prader-Willi syndrome (PWS) is a genetic disorder occurring in 1 of 10,000-16,000 live births and is characterized by excessive… (More)
Is this relevant?
Highly Cited
2000
Highly Cited
2000
Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.
Prader-Willi syndrome (PWS) is a complex neurogenetic disorder with considerable clinical variability that is thought in large… (More)
Is this relevant?
Highly Cited
1997
Highly Cited
1997
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region
Prader-Willi syndrome (PWS) is a neurogenetic disorder that results from the absence of a normal paternal contribution to the… (More)
Is this relevant?
Highly Cited
1996
Highly Cited
1996
Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.
The human SNRPN (small nuclear ribonucleoprotein polypeptide N) gene is one of a gene family that encode proteins involved in pre… (More)
Is this relevant?
Highly Cited
1995
Highly Cited
1995
Dynamic epidermal cooling during pulsed laser treatment of port-wine stain. A new methodology with preliminary clinical evaluation.
BACKGROUND AND DESIGN The clinical objective in the treatment of a patient with port-wine stain (PWS) undergoing laser therapy is… (More)
Is this relevant?
Highly Cited
1992
Highly Cited
1992
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region
Prader–Willi syndrome (PWS) is associated with paternal gene deficiencies in human chromosome 15q11–13, suggesting that PWS is… (More)
Is this relevant?