(Q24536116)

English

Mitf and Tfe3, two members of the Mitf-Tfe family of bHLH-Zip transcription factors, have important but functionally redundant roles in osteoclast development

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Mitf and Tfe3, two members of the Mitf-Tfe family of bHLH-Zip transcription factors, have important but functionally redundant roles in osteoclast development (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Transcription factor E3

1 reference

GOA release 2020-03-11

Melanogenesis associated transcription factor

1 reference

GOA release 2020-03-11

Neal G. Copeland

6

object named as

Neal G Copeland

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Nancy A. Jenkins

7

object named as

Nancy A Jenkins

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Lino Tessarollo

2

object named as

Lino Tessarollo

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

author name string

Eiríkur Steingrimsson

1

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Bhavani Pathak

3

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Ling Hou

4

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Heinz Arnheiter

5

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

language of work or name

0 references

publication date

1 April 2002

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

99

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

4477-4482

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Waardenburg syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

24 March 2017

TFEC, a basic helix-loop-helix protein, forms heterodimers with TFE3 and inhibits TFE3-dependent transcription activation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

24 March 2017

The microphthalmia transcription factor regulates expression of the tartrate-resistant acid phosphatase gene during terminal differentiation of osteoclasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

24 March 2017

nacre encodes a zebrafish microphthalmia-related protein that regulates neural-crest-derived pigment cell fate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

24 March 2017

The bHLH-Zip transcription factor Tfeb is essential for placental vascularization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

24 March 2017

Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

24 March 2017

Insight into the microphthalmia gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

24 March 2017

A helix-loop-helix transcription factor-like gene is located at the mi locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

24 March 2017

TFE3: a helix-loop-helix protein that activates transcription through the immunoglobulin enhancer muE3 motif

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

24 March 2017

Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

7 April 2017

Simplified mammalian DNA isolation procedure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

7 April 2017

Linking osteopetrosis and pycnodysostosis: regulation of cathepsin K expression by the microphthalmia transcription factor family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

TFE3, a transcription factor homologous to microphthalmia, is a potential transcriptional activator of tyrosinase and TyrpI genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

Gene-target recognition among members of the myc superfamily and implications for oncogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

Sin meets NuRD and other tails of repression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

Spontaneous transdifferentiation of quail pigmented epithelial cell is accompanied by a mutation in the Mitf gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome).

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

https://api.crossref.org/works/10.1073%2FPNAS.072071099

21 January 2018

Age-resolving osteopetrosis: a rat model implicating microphthalmia and the related transcription factor TFE3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

The absence of the transcription activator TFE3 impairs activation of B cells in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

The semidominant Mi(b) mutation identifies a role for the HLH domain in DNA binding in addition to its role in protein dimerization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

The recessive phenotype displayed by a dominant negative microphthalmia-associated transcription factor mutant is a result of impaired nucleation potential

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

Mild osteopetrosis in the microphthalmia-oak ridge mouse. A model for intermediate autosomal recessive osteopetrosis in humans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes of Mus musculus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

A morphologic study of osteoclasts isolated from osteopetrotic microphthalmic (mi/mi) mouse and human fetal long bones using an instrument permitting combination of light and scanning electron microscopy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

Allelic variation within the Emv-15 locus defines genomic sequences closely linked to the agouti locus on mouse chromosome 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

mTFE3, an X-linked transcriptional activator containing basic helix-loop-helix and zipper domains, utilizes the zipper to stabilize both DNA binding and multimerization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

27 September 2017

Repression by the Mad(Mxi1)-Sin3 complex.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

30 May 2018

Mutation at the anophthalmic white locus in Syrian hamsters: haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

30 May 2018

Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

30 May 2018

Spleen Cells Transmit Osteopetrosis in Mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=123673

30 May 2018

Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.072071099

21 January 2018

The rat microphthalmia-associated transcription factor gene (Mitf) maps at 4q34-q41 and is mutated in the mib rats

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.072071099

21 January 2018

Intrafamilial phenotypic variability in Engelmann disease (ED): are ED and Ribbing disease the same entity?

1 reference

https://pubmed.ncbi.nlm.nih.gov/11930005

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous mutation in Mitf gene causes osteopetrosis in silver homozygote quail

1 reference

https://pubmed.ncbi.nlm.nih.gov/11930005

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bone Resorption Restored in Osteopetrotic Mice by Transplants of Normal Bone Marrow and Spleen Cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/11930005

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ultrastructure of osteoclasts in microphthalmic mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/11930005

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fusion disability of embryonic osteoclast precursor cells and macrophages in the microphthalmic osteopetrotic mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/11930005

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carbonic anhydrase isozymes of osteoclasts and erythrocytes of osteopetrotic microphthalmic mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/11930005

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family

1 reference

https://pubmed.ncbi.nlm.nih.gov/11930005

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neonatal reductions in osteoclast number and function account for the transient nature of osteopetrosis in the rat mutation microphthalmia blanc (mib)

1 reference

https://pubmed.ncbi.nlm.nih.gov/11930005

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.072071099

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

2002PNAS...99.4477S

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

ResearchGate publication ID

0 references

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