Lista de obras - Hilal Özdag - Dominio Público Uruguay

A 1 Mb minimal amplicon at 8p11-12 in breast cancer identifies new candidate oncogenes

artículo científico publicado en 2005

A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia

artículo científico publicado en 2009

A novel approach for small sample size family-based association studies: sequential tests ⬇️

artículo científico publicado el 23 de marzo de 2011

Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study

artículo científico publicado en 2016

Biologic tumor behavior in pilocytic astrocytomas

artículo científico publicado en 2012

C-type lectin domain family 12, member A: A common denominator in Behçet's syndrome and acute gouty arthritis

artículo científico publicado en 2015

EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer

scientific article (publication date: 26 November 2003)

From RNA isolation to microarray analysis: Comparison of methods in FFPE tissues

artículo científico publicado en 2016

Functionally conserved effects of rapamycin exposure on zebrafish.

artículo científico

Genome Sequence of the Boron-Tolerant and -Requiring Bacterium Bacillus boroniphilus.

artículo científico publicado en 2014

Genome-wide transcriptional reorganization associated with senescence-to-immortality switch during human hepatocellular carcinogenesis

artículo científico publicado en 2013

H2AX gene does not have a modifier effect on ataxia-telangiectasia phenotype

article

Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia

artículo científico publicado en 2007

Isotopic biomarker discovery and application in translational medicine.

artículo científico publicado en 2009

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations.

artículo científico publicado en 2009

Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency

artículo científico publicado en 2016

Optimization of gene expression microarray protocol for formalin-fixed paraffin-embedded tissues

artículo científico publicado en 2016

Protocol for qRT-PCR analysis from formalin fixed paraffin embedded tissue sections from diffuse large b-cell lymphoma: Validation of the six-gene predictor score.

artículo científico publicado en 2016

Recurrent and private MYO15A mutations are associated with deafness in the Turkish population.

artículo científico publicado en 2010

Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey

artículo científico publicado en 2010

The effect of biological heterogeneity on R-CHOP treatment outcome in diffuse large B-cell lymphoma across five international regions

artículo científico publicado en 2016

p300 regulates p53-dependent apoptosis after DNA damage in colorectal cancer cells by modulation of PUMA/p21 levels

artículo científico publicado en 2004

Lista de obras de Hilal Özdag

A 1 Mb minimal amplicon at 8p11-12 in breast cancer identifies new candidate oncogenes

A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia

A novel approach for small sample size family-based association studies: sequential tests ⬇️

Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study

Biologic tumor behavior in pilocytic astrocytomas

C-type lectin domain family 12, member A: A common denominator in Behçet's syndrome and acute gouty arthritis

EMSY links the BRCA2 pathway to sporadic breast and ovarian cancer

From RNA isolation to microarray analysis: Comparison of methods in FFPE tissues

Functionally conserved effects of rapamycin exposure on zebrafish.

Genome Sequence of the Boron-Tolerant and -Requiring Bacterium Bacillus boroniphilus.

Genome-wide transcriptional reorganization associated with senescence-to-immortality switch during human hepatocellular carcinogenesis

H2AX gene does not have a modifier effect on ataxia-telangiectasia phenotype

Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia

Isotopic biomarker discovery and application in translational medicine.

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations.

Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency

Optimization of gene expression microarray protocol for formalin-fixed paraffin-embedded tissues

Protocol for qRT-PCR analysis from formalin fixed paraffin embedded tissue sections from diffuse large b-cell lymphoma: Validation of the six-gene predictor score.

Recurrent and private MYO15A mutations are associated with deafness in the Turkish population.

Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey

The effect of biological heterogeneity on R-CHOP treatment outcome in diffuse large B-cell lymphoma across five international regions

p300 regulates p53-dependent apoptosis after DNA damage in colorectal cancer cells by modulation of PUMA/p21 levels