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MEDLINE Field Tags

These two-character field tags identify fields in records that you e-mail or save to a file.

FN

File Name

VR

Version Number

PT

Publication Type

AN

PubMed ID

DT

Document Type (J = Journal)

TI

Title

FT

Foreign Title

AU

Authors

CA

Corporate Authors

SO

Source (Volume, Issue, Pages, Published)

VL

Volume

IS

Issue

PS

Pages

PY

Publication Year

PD

Publication Date

LA

Language

AB

Abstract

A2

Other Abstract

C1

Author Address

RI

Web of Science ResearcherID Number

OI

ORCID Identifier (Open Researcher and Contributor ID)

MH

MeSH Terms

SS

Citation Subset

ID

Keyword List

SD

Molecular Sequence Data

GN

Gene Symbol

CN

Chemical

NM

Personal Name Subject

SF

Space Flight Mission

SC

Research Areas

SN

International Standard Serial Number (ISSN)

U1

Usage Count (Last 180 Days)

U2

Usage Count (Since 2013)

JC

NLM Unique ID

PA

Country

GI

Grant Information

OB

Record Owner

SA

Status

IV

Investigators

NR

Number of References

RC

Date Created, Date Completed, Date Revised

NO

Comments, Corrections, Erratum

PE

Published Electronically

NT

General Notes

DI

Digital Object Identifier (DOI)

UT

ISI Unique Article Identifier

OA

Open Access Indicator

HP

ESI Hot Paper. Note that this field is valued only for ESI subscribers

HC

ESI Highly Cited Paper. Note that this field is valued only for ESI subscribers

DA

Date this report was generated

ER

[End of Record]

EF

[End of File]

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Output Records Example - Save to HTML Format

FN

Clarivate

VR

1.0

PT

J

AN

22189395

DT

Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

TI

The molecular classification of medulloblastoma: driving the next generation clinical trials.

AU

Leary, Sarah E S
Olson, James M

SO

Current opinion in pediatrics

VL

24

IS

1

PS

33-9

PY

2012

PD

2012 Feb

LA

English

AB

PURPOSE OF REVIEW: Most children diagnosed with cancer today are expected to be cured. Medulloblastoma, the most common pediatric malignant brain tumor, is an example of a disease that has benefitted from advances in diagnostic imaging, surgical techniques, radiation therapy and combination chemotherapy over the past decades. It was an incurable disease 50 years ago, but approximately 70% of children with medulloblastoma are now cured of their disease. However, the pace of increasing the cure rate has slowed over the past 2 decades, and we have likely reached the maximal benefit that can be achieved with cytotoxic therapy and clinical risk stratification. Long-term toxicity of therapy also remains significant. To increase cure rates and decrease long-term toxicity, there is great interest in incorporating biologic 'targeted' therapy into treatment of medulloblastoma, but this will require a paradigm shift in how we classify and study disease.RECENT FINDINGS: Using genome-based high-throughput analytic techniques, several groups have independently reported methods of molecular classification of medulloblastoma within the past year. This has resulted in a working consensus to view medulloblastoma as four molecular subtypes, including wingless-type murine mammary tumor virus integration site (WNT) pathway subtype, Sonic Hedgehog pathway subtype and two less well defined subtypes (groups C and D).SUMMARY: Novel classification and risk stratification based on biologic subtypes of disease will form the basis of further study in medulloblastoma and identify specific subtypes that warrant greater research focus.

C1

Seattle Children's Hospital, University of Washington School of Medicine, Washington, USA. sarah.leary@seattlechildrens.org

SS

Index Medicus

SN

1531-698X

JC

9000850

PA

United States

GI

R01CA112350 / NCI NIH HHS. R01CA114567 / NCI NIH HHS

SA

In-Process

RC

16 Jan 2012

UT

MEDLINE:22189395

ER

EF

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Default Output Fields

The following fields are default output fields that appear on the Marked List page.

  • Authors
  • Title
  • Source
  • ISSN
  • Author Identifiers

You may deselect any of these fields when you generate your output.

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