(Q28140420)

2

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N Idänheimo

3

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E Seemanová

4

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S Rosengren

5

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T P Mäkelä

6

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J Perheentupa

7

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A D Chapelle

8

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A E Lehesjoki

Mulibrey nanism, an autosomal recessive syndrome with pericardial constriction

9

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language of work or name

English

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publication date

July 2000

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published in

Nature Genetics

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volume

25

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issue

3

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page(s)

298-301

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cites work

1 reference

7 January 2021

Mulibrey nanism: three additional patients and a review of 39 patients

1 reference

7 January 2021

A case of Mulibrey nanism with associated Wilms' tumor

1 reference

7 January 2021

Mulibrey nanism and Wilms tumor

1 reference

7 January 2021

A novel zinc finger coiled-coil domain in a family of nuclear proteins

1 reference

7 January 2021

Does this have a familiar RING?

1 reference

7 January 2021

A novel repeat domain that is often associated with RING finger and B-box motifs.

1 reference

7 January 2021

Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro

1 reference

7 January 2021

Identification of a novel nuclear speckle‐type protein, SPOP

1 reference

7 January 2021

PSORT: a program for detecting sorting signals in proteins and predicting their subcellular localization

1 reference

7 January 2021

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

7 January 2021

Molecular genetics of the Finnish disease heritage.

1 reference

7 January 2021

The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8

1 reference

7 January 2021

In vivo and in vitro characterization of the B1 and B2 zinc-binding domains from the acute promyelocytic leukemia protooncoprotein PML

1 reference

7 January 2021

Identification of a RING protein that can interact in vivo with the BRCA1 gene product

1 reference

7 January 2021

Characterisation of a novel cysteine/histidine-rich metal binding domain from Xenopus nuclear factor XNF7

1 reference

7 January 2021

TIF1alpha: a possible link between KRAB zinc finger proteins and nuclear receptors

1 reference

7 January 2021

Coactivator TIF1beta interacts with transcription factor C/EBPbeta and glucocorticoid receptor to induce alpha1-acid glycoprotein gene expression

1 reference

7 January 2021

The PML-RARα fusion mRNA generated by the t(15;17) translocation in acute promyelocytic leukemia encodes a functionally altered RAR

1 reference

7 January 2021

Developmentally regulated expression of a human "finger"-containing gene encoded by the 5' half of the ret transforming gene

1 reference

7 January 2021

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

1 reference

7 January 2021

A candidate gene for familial Mediterranean fever

1 reference

7 January 2021

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

1 reference

7 January 2021

Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle

1 reference

7 January 2021

RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer

1 reference

7 January 2021

Identifiers

DOI

10.1038/77053

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

10888877

1 reference

Consolidated OpenCitations Corpus – April 2017