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Insight into the microphthalmia gene
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scholarly article
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review article
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Europe PubMed Central
title
Insight into the microphthalmia gene
(English)
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author name string
K J Moore
series ordinal
1
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language of work or name
English
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publication date
November 1995
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published in
Trends in Genetics
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volume
11
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issue
11
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page(s)
442-8
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cites work
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family
1 reference
stated in
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
based on heuristic
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Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences.
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recognition by Max of its cognate DNA through a dimeric b/HLH/Z domain
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
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Structure and function of the b/HLH/Z domain of USF
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
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inferred from DOI database lookup
TFEB has DNA-binding and oligomerization properties of a unique helix-loop-helix/leucine-zipper family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High affinity DNA-binding Myc analogs: recognition by an alpha helix
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The vit gene maps to the mi (microphthalmia) locus of the laboratory mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
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The leucine zipper of TFE3 dictates helix-loop-helix dimerization specificity
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
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mTFE3, an X-linked transcriptional activator containing basic helix-loop-helix and zipper domains, utilizes the zipper to stabilize both DNA binding and multimerization
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
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The adenovirus major late transcription factor USF is a member of the helix-loop-helix group of regulatory proteins and binds to DNA as a dimer
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https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
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Genes and deafness
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https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
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A new allele of microphthalmia induced in the mouse: microphthalmia--defective iris (midi)
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
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Bone Resorption Restored in Osteopetrotic Mice by Transplants of Normal Bone Marrow and Spleen Cells
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
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inferred from DOI database lookup
Spleen Cells Transmit Osteopetrosis in Mice
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fusion disability of embryonic osteoclast precursor cells and macrophages in the microphthalmic osteopetrotic mouse
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
based on heuristic
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The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
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inferred from DOI database lookup
Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice
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stated in
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Pleiotropic effects of a null mutation in the c-fos proto-oncogene
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
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Bone and haematopoietic defects in mice lacking c-fos
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Interaction cloning: identification of a helix-loop-helix zipper protein that interacts with c-Fos
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effect of the mi allele on mast cells, basophils, natural killer cells, and osteoclasts in C57Bl/6J mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Melanocyte-specific expression of the human tyrosinase promoter: activation by the microphthalmia gene product and role of the initiator.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Microphthalmia-associated transcription factor as a regulator for melanocyte-specific transcription of the human tyrosinase gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2989143-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0168-9525(00)89143-X
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PubMed publication ID
8578601
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