(Q30856368)

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Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines

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Europe PubMed Central

PMC publication ID

12 September 2017

Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines (English)

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

author name string

Piras G

1

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

El Kharroubi A

2

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Europe PubMed Central

PMC publication ID

12 September 2017

Kozlov S

3

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Escalante-Alcalde D

4

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Hernandez L

5

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Copeland NG

6

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Gilbert DJ

7

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Jenkins NA

8

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Stewart CL

9

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Europe PubMed Central

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12 September 2017

language of work or name

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publication date

1 May 2000

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Europe PubMed Central

PMC publication ID

12 September 2017

Molecular and Cellular Biology

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Europe PubMed Central

PMC publication ID

12 September 2017

20

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Europe PubMed Central

PMC publication ID

12 September 2017

9

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

3308-3315

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (approximately 5.4 Mb) interval on chromosome 6q.

1 reference

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Comparisons of genomic structures and chromosomal locations of the mouse aldose reductase and aldose reductase-like genes

1 reference

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Evidence against a major role of PEG1/MEST in Silver-Russell syndrome

1 reference

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21 June 2018

hZAC encodes a zinc finger protein with antiproliferative properties and maps to a chromosomal region frequently lost in cancer

1 reference

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Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene

1 reference

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A mouse model for Prader-Willi syndrome imprinting-centre mutations

1 reference

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Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=85624

21 June 2018

epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D

1 reference

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Screening for imprinted genes by allelic message display: identification of a paternally expressed gene impact on mouse chromosome 18

1 reference

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Regulation of apoptosis and cell cycle arrest by Zac1, a novel zinc finger protein expressed in the pituitary gland and the brain

1 reference

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The laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoform

1 reference

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Identification of a zinc-finger gene at 6q25: a chromosomal region implicated in development of many solid tumors

1 reference

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Muscular dystrophies and the dystrophin-glycoprotein complex

1 reference

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Multiple mouse chromosomal loci for dynein-based motility

1 reference

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Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries

1 reference

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Production of chimeras between embryonic stem cells and embryos.

1 reference

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21 June 2018

Expression and methylation of imprinted genes during in vitro differentiation of mouse parthenogenetic and androgenetic embryonic stem cell lines

1 reference

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A functional analysis of imprinting in parthenogenetic embryonic stem cells.

1 reference

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21 June 2018

Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting

1 reference

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21 June 2018

Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality

1 reference

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21 June 2018

Genomic imprinting of Mash2, a mouse gene required for trophoblast development

1 reference

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21 June 2018

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=85624

21 June 2018

Completion of mouse embryogenesis requires both the maternal and paternal genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=85624

21 June 2018

Role of paternal and maternal genomes in mouse development

1 reference

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

1 reference

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Differential activity of maternally and paternally derived chromosome regions in mice

1 reference

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Expression of retroviral vectors in transgenic mice obtained by embryo infection

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Expression of foreign genes from retroviral vectors in mouse teratocarcinoma chimaeras.

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Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: implications for genetic imprinting

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Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome

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Development and applications of a molecular genetic linkage map of the mouse genome

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Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

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A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross

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The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

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Loss of expression of the candidate tumor suppressor gene ZAC in breast cancer cell lines and primary tumors

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High resolution mapping of chromosome 6 deletions in cervical cancer.

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Loss of heterozygosity on the long arm of chromosome 6 in breast cancer: possibly four regions of deletion

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Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

1 reference

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Localisation of the imprinted gene neuronatin, Nnat, confirms and refines the location of a second imprinting region on mouse chromosome 2.

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Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M.

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Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting

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Genetics of silver-russell syndrome

1 reference

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Detection of frequent allelic loss of 6q23-q25.2 in microdissected human breast cancer tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/10757814

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based on heuristic

inferred from PubMed ID database lookup

Molecular cytogenetics of a de novo interstitial deletion of chromosome arm 6q in a developmentally normal girl

1 reference

https://pubmed.ncbi.nlm.nih.gov/10757814

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/10757814

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/10757814

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/MCB.20.9.3308-3315.2000

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

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