(Q24564082)

English

Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function

scientific article

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15273283%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15273283%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

sudden infant death-dysgenesis of the testes syndrome

1 reference

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inferred from title

Charles Robert Flynn

15

1 reference

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31 December 2019

author name string

Erik G Puffenberger

1

1 reference

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31 December 2019

Diane Hu-Lince

2

1 reference

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31 December 2019

Jennifer M Parod

3

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31 December 2019

David W Craig

4

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31 December 2019

Seth E Dobrin

5

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31 December 2019

Andrew R Conway

6

1 reference

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31 December 2019

Elizabeth A Donarum

7

1 reference

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31 December 2019

Kevin A Strauss

8

1 reference

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31 December 2019

Travis Dunckley

9

1 reference

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31 December 2019

Javier F Cardenas

10

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31 December 2019

Kara R Melmed

11

1 reference

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31 December 2019

Courtney A Wright

12

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31 December 2019

Winnie Liang

13

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31 December 2019

Phillip Stafford

14

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31 December 2019

D Holmes Morton

16

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31 December 2019

Dietrich A Stephan

17

1 reference

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31 December 2019

language of work or name

0 references

publication date

23 July 2004

1 reference

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31 December 2019

Proceedings of the National Academy of Sciences of the United States of America

1 reference

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31 December 2019

101

1 reference

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31 December 2019

11689-11694

1 reference

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31 December 2019

32

1 reference

Europe PubMed Central

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31 December 2019

Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

24 March 2017

Testis-specific protein, Y-encoded (TSPY) expression in testicular tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

24 March 2017

A role for nucleosome assembly protein 1 in the nuclear transport of histones H2A and H2B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

24 March 2017

Identification and molecular cloning of yeast homolog of nucleosome assembly protein I which facilitates nucleosome assembly in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

24 March 2017

Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

24 March 2017

Characterization of single-nucleotide polymorphisms in coding regions of human genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

24 March 2017

Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

27 September 2017

Reflex mechanisms in gastroesophageal reflux disease and asthma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

27 September 2017

Genetic heritage of the Old Order Mennonites of southeastern Pennsylvania

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

27 September 2017

Medullary serotonergic network deficiency in the sudden infant death syndrome: review of a 15-year study of a single dataset

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

27 September 2017

Paroxysmal vagal overactivity, apparent life-threatening event and sudden infant death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

27 September 2017

Murine and human TSPYL genes: novel members of the TSPY-SET-NAP1L1 family

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=511011

27 September 2017

https://api.crossref.org/works/10.1073%2FPNAS.0401194101

21 January 2018

Large-scale genotyping of complex DNA.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0401194101

21 January 2018

High-resolution haplotype structure in the human genome

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0401194101

21 January 2018

Xenopus nucleosome assembly protein becomes tissue-restricted during development and can alter the expression of specific genes.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0401194101

21 January 2018

cDNA cloning of the E1 alpha subunit of the branched-chain alpha-keto acid dehydrogenase and elucidation of a molecular basis for maple syrup urine disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15273283

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.0401194101

1 reference

Europe PubMed Central

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31 December 2019

2004PNAS..10111689P

0 references

1 reference

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31 December 2019

1 reference

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31 December 2019

ResearchGate publication ID

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