Haploinsufficiency of NSD1 causes Sotos syndrome (Q34118696)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Haploinsufficiency of NSD1 causes Sotos syndrome	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Haploinsufficiency of NSD1 causes Sotos syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Haploinsufficiency

0 references

22

object named as

Norio Niikawa

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Akira Kinoshita

16

object named as

Akira Kinoshita

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

10

object named as

Yoshio Makita

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Tomoko Hasegawa

13

object named as

Tomoko Hasegawa

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

12

object named as

Tohru Sonoda

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

19

object named as

Tohru Ohta

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Naohiro Kurotaki

1

object named as

Naohiro Kurotaki

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

5

object named as

Tatsuro Kondoh

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

8

object named as

Kenji Naritomi

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Tatsuya Kishino

20

object named as

Tatsuya Kishino

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

Kiyoshi Imaizumi

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Naoki Harada

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Mitsuo Masuno

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Toshiro Nagai

6

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Hirofumi Ohashi

7

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Masato Tsukahara

9

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Tateo Sugimoto

11

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Yasuaki Chinen

14

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Hiro-aki Tomita Ha

15

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Tsuyoshi Mizuguchi

17

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Koh-ichiro Yoshiura Ki

18

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Yoshimitsu Fukushima

21

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Naomichi Matsumoto

23

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

language of work or name

0 references

publication date

18 March 2002

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Nature Genetics

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

30

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

365-366

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Sotos syndrome associated with a de novo balanced reciprocal translocation t(5;8)(q35;q24.1).

1 reference

https://api.crossref.org/works/10.1038%2FNG863

7 January 2021

based on heuristic

inferred from DOI database lookup

Two distinct nuclear receptor interaction domains in NSD1, a novel SET protein that exhibits characteristics of both corepressors and coactivators

1 reference

https://api.crossref.org/works/10.1038%2FNG863

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular characterization of NSD1, a human homologue of the mouse Nsd1 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG863

7 January 2021

based on heuristic

inferred from DOI database lookup

SET domain proteins modulate chromatin domains in eu- and heterochromatin.

1 reference

https://api.crossref.org/works/10.1038%2FNG863

7 January 2021

based on heuristic

inferred from DOI database lookup

The PWWP domain: a potential protein-protein interaction domain in nuclear proteins influencing differentiation?

1 reference

https://api.crossref.org/works/10.1038%2FNG863

7 January 2021

based on heuristic

inferred from DOI database lookup

The PHD finger: implications for chromatin-mediated transcriptional regulation

1 reference

https://api.crossref.org/works/10.1038%2FNG863

7 January 2021

based on heuristic

inferred from DOI database lookup

The syndromes of Sotos and Weaver: reports and review

1 reference

https://api.crossref.org/works/10.1038%2FNG863

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial Sotos syndrome (cerebral gigantism): craniofacial and psychological characteristics.

1 reference

https://api.crossref.org/works/10.1038%2FNG863

7 January 2021

based on heuristic

inferred from DOI database lookup

Sotos syndrome in two brothers.

1 reference

https://api.crossref.org/works/10.1038%2FNG863

7 January 2021

based on heuristic

inferred from DOI database lookup

Letter: Cerebral gigantism

1 reference

https://api.crossref.org/works/10.1038%2FNG863

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34118696&oldid=2196274350"