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IDS wt Allele
Known as:
Iduronate 2-Sulfatase (Hunter Syndrome) wt Allele
, MPS2
, SIDS
Human IDS wild-type allele is located in the vicinity of Xq28 and is approximately 27 kb in length. This allele, which encodes iduronate 2-sulfatase…
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National Institutes of Health
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Related topics
Related topics
6 relations
Carbohydrate Metabolism
Homo sapiens
Hydrolysis
Mucopolysaccharidosis II
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Broader (1)
IDS gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2013
Highly Cited
2013
A scaling approach to project regional sea level rise and its uncertainties
M. Perrette
,
F. Landerer
,
R. Riva
,
K. Frieler
,
M. Meinshausen
2013
Corpus ID: 7790007
Abstract. Climate change causes global mean sea level to rise due to thermal expansion of seawater and loss of land ice from…
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Highly Cited
2009
Highly Cited
2009
Hazardous cosleeping environments and risk factors amenable to change: case-control study of SIDS in south west England
P. Blair
,
P. Sidebotham
,
Carol Evason-Coombe
,
Margaret Edmonds
,
Ellen M. A. Heckstall-Smith
,
P. Fleming
British medical journal
2009
Corpus ID: 13338345
Objectives To investigate the factors associated with sudden infant death syndrome (SIDS) from birth to age 2 years, whether…
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Highly Cited
2006
Highly Cited
2006
A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y.
L. Plant
,
P. Bowers
,
+6 authors
S. Goldstein
Journal of Clinical Investigation
2006
Corpus ID: 24790623
Thousands die each year from sudden infant death syndrome (SIDS). Neither the cause nor basis for varied prevalence in different…
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Highly Cited
2003
Highly Cited
2003
Characterization of successful and failed autoresuscitation in human infants, including those dying of SIDS
R. Sridhar
,
B. Thach
,
D. Kelly
,
Judith A. Henslee
Pediatric Pulmonology
2003
Corpus ID: 2643432
Our purpose was to identify and further characterize physiologic mechanisms relevant to autoresuscitation from hypoxic apnea in…
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Highly Cited
2003
Highly Cited
2003
Sudden infant death syndrome: Association with a promoter polymorphism of the serotonin transporter gene
D. Weese-Mayer
,
E. Berry-Kravis
,
B. Maher
,
J. Silvestri
,
M. Curran
,
M. Marazita
American Journal of Medical Genetics. Part A
2003
Corpus ID: 2035024
Serotonergic receptor binding in the arcuate nucleus, n. raphé obscurus, and other medullary regions is decreased in sudden…
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Review
2000
Review
2000
Sudden Infant Death Syndrome: A Failure of Compensatory Cerebellar Mechanisms?
R. Harper
Pediatric Research
2000
Corpus ID: 2631766
The mechanisms underlying failure in sudden infant death syndrome may involve inadequate compensatory motor responses to a…
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Highly Cited
1999
Highly Cited
1999
Neuronal Apoptosis in Sudden Infant Death Syndrome
K. Waters
,
B. Meehan
,
Jing-Qi Huang
,
R. Gravel
,
J. Michaud
,
A. Côté
Pediatric Research
1999
Corpus ID: 23567739
Although evidence shows that victims of sudden infant death syndrome (SIDS) suffer repetitive episodes of hypoxemia, only subtle…
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Highly Cited
1998
Highly Cited
1998
Brainstem 3H-Nicotine Receptor Binding in the Sudden Infant Death Syndrome
D. B. Nachmanoff
,
A. Panigrahy
,
+6 authors
H. Kinney
Journal of Neuropathology and Experimental…
1998
Corpus ID: 25545008
Maternal cigarette smoking during pregnancy has been shown to be a major risk factor for the sudden infant death syndrome (SIDS…
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Highly Cited
1994
Highly Cited
1994
Reduction in mortality from sudden infant death syndrome in New Zealand: 1986-92.
E. A. Mitchell
,
J. M. Brunt
,
C. Everard
Archives of Disease in Childhood
1994
Corpus ID: 40421659
Mortality from sudden infant death syndrome (SIDS, or cot death) in New Zealand has been high by international standards (4/1000…
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Highly Cited
1985
Highly Cited
1985
Brainstem immaturity in sudden infant death syndrome: A quantitative rapid Golgi study of dendritic spines in 95 infants
Quattrochi Jj
,
McBride Pt
,
A. Yates
Brain Research
1985
Corpus ID: 19779744
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