JEB protocol

Known as: JEB, Bleomycin/Carboplatin/Etoposide, JM8-Etoposide-Bleomycin Regimen 
An abbreviation for a chemotherapy combination used to treat childhood ovarian and testicular germ cell cancers that have spread. It includes the… (More)
National Institutes of Health

Papers overview

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Review
2014
Review
2014
BACKGROUND Several new targeted genes and clinical subtypes have been identified since publication in 2008 of the report of the… (More)
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Highly Cited
2006
Highly Cited
2006
Whether alpha6beta4 integrin regulates migration remains controversial. beta4 integrin-deficient (JEB) keratinocytes display… (More)
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2001
2001
Junctional epidermolysis bullosa (JEB) is a group of heritable blistering diseases in which tissue separation occurs within the… (More)
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Highly Cited
1997
Highly Cited
1997
Integrins alpha3beta1 and alpha6beta4 are abundant receptors on keratinocytes for laminin-5, a major component of the basement… (More)
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Highly Cited
1997
Highly Cited
1997
The alpha6 integrin subunit participates in the formation of both alpha6beta1 and alpha6beta4 laminin receptors, which have been… (More)
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Highly Cited
1995
Highly Cited
1995
Junctional epidermolysis bullosa (JEB) is a heterogeneous autosomal recessively inherited blistering skin disorder associated… (More)
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Highly Cited
1995
Highly Cited
1995
The inherited mechanobullous disorder, junctional epidermolysis bullosa (JEB), is characterized by extensive blistering and… (More)
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Highly Cited
1994
Highly Cited
1994
We have linked Herlitz's junctional epidermolysis bullosa (H–JEB) to the gene (LAMC2) encoding the γ2 subunit of nicein/kalinin… (More)
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Highly Cited
1994
Highly Cited
1994
Junctional epidermolysis bullosa (JEB) is an autosomal recessive disorder characterized by blister formation within the dermal… (More)
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Highly Cited
1994
Highly Cited
1994
Herlitz junctional epidermolysis bullosa (H-JEB) is a severe autosomal recessive disorder characterized by blister formation… (More)
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