(Q24294774)

GOA release 2020-03-11

53

Nicholas Katsanis

Nicholas

Katsanis

1 reference

19 October 2023

Friedhelm Hildebrandt

73

object named as

Friedhelm Hildebrandt

Friedhelm

Thillai Sivakumar Natarajan

Hildebrandt

1 reference

19 October 2023

58

Heymut Omran

Heymut

Omran

1 reference

19 October 2023

40

Corinne Antignac

Corinne

Antignac

1 reference

19 October 2023

29

Bernhard Schermer

Bernhard

Schermer

1 reference

19 October 2023

31

Thomas Benzing

Thomas

Benzing

1 reference

19 October 2023

39

Sophie Saunier

Sophie

Saunier

1 reference

19 October 2023

22

Ronald Roepman

Ronald

Roepman

1 reference

19 October 2023

71

Agata Smogorzewska

Agata

Smogorzewska

1 reference

19 October 2023

Rudel Saunders

62

Rudel

Saunders

1 reference

19 October 2023

Sabine Janssen

34

Sabine

Janssen

1 reference

19 October 2023

Max C Liebau

30

Max C

Liebau

1 reference

19 October 2023

John A Sayer

28

John A

Sayer

1 reference

19 October 2023

Edgar A Otto

72

Edgar A

Otto

1 reference

19 October 2023

Shawn Levy

70

Shawn

Levy

1 reference

19 October 2023

Massimo Attanasio

38

Massimo

Attanasio

1 reference

19 October 2023

Christelle Golzio

52

Christelle

Golzio

1 reference

19 October 2023

Joann M Sekiguchi

61

Joann M

Sekiguchi

1 reference

19 October 2023

Heon Yung Gee

11

Heon Yung

Gee

1 reference

19 October 2023

Rachel H Giles

4

Rachel H

Giles

1 reference

19 October 2023

48

Joseph G Gleeson

Joseph G

Gleeson

1 reference

19 October 2023

7

Hui Wang

Hui

Wang

1 reference

19 October 2023

49

Sharon P Andreoli

Sharon P

Andreoli

1 reference

19 October 2023

19

Jeroen van Reeuwijk

Jeroen

van Reeuwijk

1 reference

19 October 2023

41

Robert K Koenekoop

Robert K

Koenekoop

1 reference

19 October 2023

69

Peter Nurnberg

Peter

Nurnberg

1 reference

19 October 2023

8

Toby W Hurd

Toby W

Hurd

1 reference

19 October 2023

43

Irma Lopez

Irma

Lopez

1 reference

19 October 2023

1

Moumita Chaki

Moumita

Chaki

1 reference

19 October 2023

2

Rannar Airik

Rannar

Airik

1 reference

19 October 2023

12

Gokul Ramaswami

Gokul

Ramaswami

1 reference

19 October 2023

18

Heleen H Arts

Heleen H

Arts

1 reference

19 October 2023

21

Stef J F Letteboer

Stef J F

Letteboer

1 reference

19 October 2023

26

Gerd Walz

Gerd

Walz

1 reference

19 October 2023

33

Iain Drummond

Iain

Drummond

1 reference

19 October 2023

36

Sivakumar Natarajan

Sivakumar

Natarajan

1 reference

19 October 2023

45

Corinne Stoetzel

Corinne

Stoetzel

1 reference

19 October 2023

68

Gudrun Nurnberg

Gudrun

Nurnberg

1 reference

19 October 2023

46

Helene Dollfus

Helene

Dollfus

1 reference

19 October 2023

Amiya K Ghosh

3

Amiya K

Ghosh

1 reference

19 October 2023

Rui Chen

5

Rui

Chen

1 reference

19 October 2023

Gisela G Slaats

6

Gisela G

Slaats

1 reference

19 October 2023

Weibin Zhou

9

Weibin

Zhou

1 reference

19 October 2023

Andrew Cluckey

10

Andrew

Cluckey

1 reference

19 October 2023

Chen-Jei Hong

13

Chen-Jei

Hong

1 reference

19 October 2023

Bruce A Hamilton

14

Bruce A

Hamilton

1 reference

19 October 2023

Igor Cervenka

15

Igor

Cervenka

1 reference

19 October 2023

Ranjani Sri Ganji

16

Ranjani Sri

Ganji

1 reference

19 October 2023

Vitezslav Bryja

17

Vitezslav

Bryja

1 reference

19 October 2023

Machteld M Oud

20

Machteld M

Oud

1 reference

19 October 2023

Hervé Husson

23

Hervé

Husson

1 reference

19 October 2023

Oxana Ibraghimov-Beskrovnaya

24

Oxana

Ibraghimov-Beskrovnaya

1 reference

19 October 2023

Takayuki Yasunaga

25

Takayuki

Yasunaga

1 reference

19 October 2023

Lorraine Eley

27

Lorraine

Eley

1 reference

19 October 2023

Stephanie Le Corre

32

Stephanie

Le Corre

1 reference

19 October 2023

Susan J Allen

35

Susan J

Allen

1 reference

19 October 2023

John F O'Toole

37

John F

O'Toole

1 reference

19 October 2023

Huanan Ren

42

Huanan

Ren

1 reference

19 October 2023

Ahmet Nayir

44

Ahmet

Nayir

1 reference

19 October 2023

Rustin Massoudi

47

Rustin

Massoudi

1 reference

19 October 2023

Dan G Doherty

50

Dan G

Doherty

1 reference

19 October 2023

Anna Lindstrad

51

Anna

Lindstrad

1 reference

19 October 2023

Lars Pape

54

Lars

Pape

1 reference

19 October 2023

Emad B Abboud

55

Emad B

Abboud

1 reference

19 October 2023

Ali A Al-Rajhi

56

Ali A

Al-Rajhi

1 reference

19 October 2023

Richard A Lewis

57

Richard A

Lewis

1 reference

19 October 2023

Eva Y-H P Lee

59

Eva Y-H P

Lee

1 reference

19 October 2023

Shaohui Wang

60

Shaohui

Wang

1 reference

19 October 2023

Colin A Johnson

63

Colin A

Johnson

1 reference

19 October 2023

Elizabeth Garner

64

Elizabeth

Garner

1 reference

19 October 2023

Katja Vanselow

65

Katja

Vanselow

1 reference

19 October 2023

Jens S Andersen

66

Jens S

Andersen

1 reference

19 October 2023

Joseph Shlomai

67

Joseph

on focus list of Wikimedia project

Shlomai

1 reference

19 October 2023

language of work or name

English

0 references

publication date

3 August 2012

0 references

published in

Cell

0 references

volume

150

0 references

issue

3

0 references

page(s)

533-48

0 references

ScienceSource

0 references

cites work

Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Acetylation and phosphorylation of SRSF2 control cell fate decision in response to cisplatin

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

CEP152 is a genome maintenance protein disrupted in Seckel syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Targeted capture and massively parallel sequencing of 12 human exomes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

A mouse model of ATR-Seckel shows embryonic replicative stress and accelerated aging

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

A systematic approach to mapping recessive disease genes in individuals from outbred populations

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Drosophila asterless and vertebrate Cep152 Are orthologs essential for centriole duplication

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Cep164 is a mediator protein required for the maintenance of genomic stability through modulation of MDC1, RPA, and CHK1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Cep164, a novel centriole appendage protein required for primary cilium formation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

p53 activation by knockdown technologies

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

The transcription factor Zfp423/OAZ is required for cerebellar development and CNS midline patterning.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Zfp423 controls proliferation and differentiation of neural precursors in cerebellar vermis formation.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Proteomic characterization of the human centrosome by protein correlation profiling

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

A single ataxia telangiectasia gene with a product similar to PI-3 kinase

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

The DNA Damage Response: Making It Safe to Play with Knives

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Nuclear tau, a key player in neuronal DNA protection

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Genetic and physical interaction between the NPHP5 and NPHP6 gene products

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Mutations in the pericentrin (PCNT) gene cause primordial dwarfism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

The KLHL12-Cullin-3 ubiquitin ligase negatively regulates the Wnt-beta-catenin pathway by targeting Dishevelled for degradation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Poly(ADP-ribose) polymerase 1 interacts with OAZ and regulates BMP-target genes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

A Wnt7b-dependent pathway regulates the orientation of epithelial cell division and establishes the cortico-medullary axis of the mammalian kidney

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Cilia and Hedgehog responsiveness in the mouse

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Hedgehog signalling in the mouse requires intraflagellar transport proteins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Identification of DNA recognition sequences and protein interaction domains of the multiple-Zn-finger protein Roaz

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Parametric and nonparametric linkage analysis: a unified multipoint approach

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Pericentrin, a highly conserved centrosome protein involved in microtubule organization

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

The proteome of the mouse photoreceptor sensory cilium complex

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Allegro, a new computer program for multipoint linkage analysis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Genotype-phenotype correlation in 440 patients with NPHP-related ciliopathies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient mice

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Is post-transcriptional stabilization, splicing and translation of selective mRNAs a key to the DNA damage response?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Functional genomic screens identify CINP as a genome maintenance protein

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

UV-dependent interaction between Cep164 and XPA mediates localization of Cep164 at sites of DNA damage and UV sensitivity

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Nephronophthisis: disease mechanisms of a ciliopathy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

A critical developmental switch defines the kinetics of kidney cyst formation after loss of Pkd1

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

PML protein association with specific nucleolar structures differs in normal, tumor and senescent human cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Cdk inhibition in human cells compromises chk1 function and activates a DNA damage response.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Checking out the centrosome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Cell-cycle-dependent three-dimensional redistribution of nuclear proteins, P 120, pKi-67, and SC 35 splicing factor, in the presence of the topoisomerase I inhibitor camptothecin.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Splicing regulator SC35 is essential for genomic stability and cell proliferation during mammalian organogenesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Association of adipogenic genes with SC-35 domains during porcine adipogenesis

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Mutation analysis of NPHP6/CEP290 in patients with Joubert syndrome and Senior-Løken syndrome

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Long-lasting arrest of murine polycystic kidney disease with CDK inhibitor roscovitine.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

Defective planar cell polarity in polycystic kidney disease

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3433835

29 November 2018

Linking cilia to Wnts

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22863007

12 December 2020

inferred from PubMed ID database lookup

Versatile screening for binary protein-protein interactions by yeast two-hybrid mating

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2012.06.028

7 January 2021

Accurate whole human genome sequencing using reversible terminator chemistry

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2012.06.028

7 January 2021

Beta-arrestin is a necessary component of Wnt/beta-catenin signaling in vitro and in vivo.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2012.06.028

7 January 2021

Nephrocystin-4 regulates Pyk2-induced tyrosine phosphorylation of nephrocystin-1 to control targeting to monocilia

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2012.06.028

7 January 2021

NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2012.06.028

7 January 2021

Functional characterization of the OFD1 protein reveals a nuclear localization and physical interaction with subunits of a chromatin remodeling complex

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2012.06.028

7 January 2021

The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2012.06.028

7 January 2021

Nephrocystin-3 is required for ciliary function in zebrafish embryos

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2012.06.028

7 January 2021

Wnt-5a induces Dishevelled phosphorylation and dopaminergic differentiation via a CK1-dependent mechanism

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2012.06.028

7 January 2021

Development of polycystic kidney disease in juvenile cystic kidney mice: insights into pathogenesis, ciliary abnormalities, and common features with human disease.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2012.06.028

7 January 2021

10.1016/J.CELL.2012.06.028

Identifiers

DOI

1 reference

release_oc5oqvgolncmjix2czcnklvq74

569911

Fatcat ID

0 references

569911

1 reference

1 reference

1 reference