Lista de obras - Mina Ohadi - Dominio Público Uruguay

A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.

artículo científico publicado en 2015

A mutation in the calreticulin gene promoter in a family case of schizoaffective disorder leads to its aberrant transcriptional activation

artículo científico publicado en 2008

A novel polymorphic purine complex at the 1.5 kb upstream region of the human caveolin-1 gene and risk of Alzheimer's disease; extra-short alleles and accumulated allele homozygosity

artículo científico publicado en 2009

A point mutation at the calreticulin gene core promoter conserved sequence in a case of schizophrenia.

artículo científico publicado en 2006

A primate-specific functional GTTT-repeat in the core promoter of CYTH4 is linked to bipolar disorder in human

artículo científico publicado en 2014

Aberrant expression of Activating Transcription Factor 6 (ATF6) in major psychiatric disorders.

artículo científico publicado en 2012

An exceptionally long CA-repeat in the core promoter of SCGB2B2 links with the evolution of apes and Old World monkeys.

artículo científico publicado en 2015

Association analysis of the dopamine transporter (DAT1)-67A/T polymorphism in bipolar disorder

artículo científico publicado en 2005

Association between polymorphisms in Interleukin-16 gene and risk of late-onset Alzheimer's disease.

artículo científico publicado en 2015

Association between the DRD2 A1 allele and opium addiction in the Iranian population

artículo científico publicado en 2005

Attention-deficit/hyperactivity disorder (ADHD) association with the DAT1 core promoter -67 T allele

artículo científico publicado en 2006

BEND3 is involved in the human-specific repression of calreticulin: Implication for the evolution of higher brain functions in human

artículo científico publicado en 2015

Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson's disease.

artículo científico publicado en 2013

Core promoter STRs: novel mechanism for inter-individual variation in gene expression in humans.

artículo científico publicado en 2011

Core promoter short tandem repeats as evolutionary switch codes for primate speciation.

artículo científico publicado en 2014

Decreased gene expression activity as a result of a mutation in the calreticulin gene promoter in a family case of schizoaffective disorder

artículo científico publicado en 2015

Dominant and Protective Role of the CYTH4 Primate-Specific GTTT-Repeat Longer Alleles Against Neurodegeneration

artículo científico publicado en 2015

Evolutionary trend of exceptionally long human core promoter short tandem repeats.

artículo científico publicado en 2012

Exceptional expansion and conservation of a CT-repeat complex in the core promoter ofPAXBP1in primates

scientific article published on 21 February 2014

Exceptional human core promoter nucleotide compositions

artículo científico publicado en 2011

Exceptionally long 5' UTR short tandem repeats specifically linked to primates.

artículo científico publicado en 2015

Gender dimorphism in the DAT1 -67 T-allele homozygosity and predisposition to bipolar disorder

artículo científico publicado en 2007

Genome-wide identification of human- and primate-specific core promoter short tandem repeats

artículo científico publicado en 2016

Haplotypes across the human caveolin 1 gene upstream purine complex significantly alter gene expression: implication in neurodegenerative disorders.

artículo científico publicado en 2012

Link between short tandem repeats and translation initiation site selection

scientific article published on 29 October 2018

Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping

artículo científico publicado en 1999

Mutation analysis of the DBC2 gene in sporadic and familial breast cancer

artículo científico publicado en 2007

No association between the DAT1 10-repeat allele and ADHD in the Iranian population

artículo científico publicado en 2008

Novel evidence of the involvement of calreticulin in major psychiatric disorders ⬇️

artículo científico publicado el 21 de febrero de 2012

Novel extreme homozygote haplotypes at the human caveolin 1 gene upstream purine complex in sporadic Alzheimer's disease.

artículo científico publicado en 2010

Novel mutations in the calreticulin gene core promoter and coding sequence in schizoaffective disorder.

artículo científico publicado en 2010

Polymorphic core promoter GA-repeats alter gene expression of the early embryonic developmental genes.

artículo científico publicado en 2013

Proposed minimal essential co-expression and physical interaction networks involved in the development of cognition impairment in human mid and late life

artículo científico publicado en 2020

RIT2 Polymorphisms: Is There a Differential Association?

artículo científico publicado en 2016

Reversion of the human calreticulin gene promoter to the ancestral type as a result of a novel psychosis-associated mutation

article

Skewing of the genetic architecture at the ZMYM3 human-specific 5' UTR short tandem repeat in schizophrenia

artículo científico publicado en 2018

Support for down-tuning of the calreticulin gene in the process of human evolution.

artículo científico publicado en 2011

The human caveolin 1 gene upstream purine complex and neurodegeneration--a common signature

artículo científico publicado en 2011

Lista de obras de Mina Ohadi

A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.

A mutation in the calreticulin gene promoter in a family case of schizoaffective disorder leads to its aberrant transcriptional activation

A novel polymorphic purine complex at the 1.5 kb upstream region of the human caveolin-1 gene and risk of Alzheimer's disease; extra-short alleles and accumulated allele homozygosity

A point mutation at the calreticulin gene core promoter conserved sequence in a case of schizophrenia.

A primate-specific functional GTTT-repeat in the core promoter of CYTH4 is linked to bipolar disorder in human

Aberrant expression of Activating Transcription Factor 6 (ATF6) in major psychiatric disorders.

An exceptionally long CA-repeat in the core promoter of SCGB2B2 links with the evolution of apes and Old World monkeys.

Association analysis of the dopamine transporter (DAT1)-67A/T polymorphism in bipolar disorder

Association between polymorphisms in Interleukin-16 gene and risk of late-onset Alzheimer's disease.

Association between the DRD2 A1 allele and opium addiction in the Iranian population

Attention-deficit/hyperactivity disorder (ADHD) association with the DAT1 core promoter -67 T allele

BEND3 is involved in the human-specific repression of calreticulin: Implication for the evolution of higher brain functions in human

Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson's disease.

Core promoter STRs: novel mechanism for inter-individual variation in gene expression in humans.

Core promoter short tandem repeats as evolutionary switch codes for primate speciation.

Decreased gene expression activity as a result of a mutation in the calreticulin gene promoter in a family case of schizoaffective disorder

Dominant and Protective Role of the CYTH4 Primate-Specific GTTT-Repeat Longer Alleles Against Neurodegeneration

Evolutionary trend of exceptionally long human core promoter short tandem repeats.

Exceptional expansion and conservation of a CT-repeat complex in the core promoter ofPAXBP1in primates

Exceptional human core promoter nucleotide compositions

Exceptionally long 5' UTR short tandem repeats specifically linked to primates.

Gender dimorphism in the DAT1 -67 T-allele homozygosity and predisposition to bipolar disorder

Genome-wide identification of human- and primate-specific core promoter short tandem repeats

Haplotypes across the human caveolin 1 gene upstream purine complex significantly alter gene expression: implication in neurodegenerative disorders.

Link between short tandem repeats and translation initiation site selection

Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping

Mutation analysis of the DBC2 gene in sporadic and familial breast cancer

No association between the DAT1 10-repeat allele and ADHD in the Iranian population

Novel evidence of the involvement of calreticulin in major psychiatric disorders ⬇️

Novel extreme homozygote haplotypes at the human caveolin 1 gene upstream purine complex in sporadic Alzheimer's disease.

Novel mutations in the calreticulin gene core promoter and coding sequence in schizoaffective disorder.

Polymorphic core promoter GA-repeats alter gene expression of the early embryonic developmental genes.

Proposed minimal essential co-expression and physical interaction networks involved in the development of cognition impairment in human mid and late life

RIT2 Polymorphisms: Is There a Differential Association?

Reversion of the human calreticulin gene promoter to the ancestral type as a result of a novel psychosis-associated mutation

Skewing of the genetic architecture at the ZMYM3 human-specific 5' UTR short tandem repeat in schizophrenia

Support for down-tuning of the calreticulin gene in the process of human evolution.

The human caveolin 1 gene upstream purine complex and neurodegeneration--a common signature