Lista de obras - Lamis Yehia - Dominio Público Uruguay

A Nonpump Function of Sodium Iodide Symporter in Thyroid Cancer via Cross-talk with PTEN Signaling

scientific article published on 14 September 2018

Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors

artículo científico publicado en 2020

Distinct Alterations in Tricarboxylic Acid Cycle Metabolites Associate with Cancer and Autism Phenotypes in Cowden Syndrome and Bannayan-Riley-Ruvalcaba Syndrome

scientific article published on 26 September 2019

Epidermal growth factor receptor and KRAS mutations in lung adenocarcinoma: a retrospective study of the Lebanese population.

artículo científico publicado en 2014

Exome Sequencing Reveals Germline SMAD9 Mutation That Reduces Phosphatase and Tensin Homolog Expression and Is Associated With Hamartomatous Polyposis and Gastrointestinal Ganglioneuromas.

artículo científico publicado en 2015

Exome sequencing reveals germline gain-of-function EGFR mutation in an adult with Lhermitte-Duclos disease.

artículo científico publicado en 2016

Expression of HIF-1α and Markers of Angiogenesis Are Not Significantly Different in Triple Negative Breast Cancer Compared to Other Breast Cancer Molecular Subtypes: Implications for Future Therapy

artículo científico publicado en 2015

Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer

scientific journal article

Germline TTN variants are enriched in PTEN-wildtype Bannayan-Riley-Ruvalcaba syndrome.

artículo científico publicado en 2017

Germline compound heterozygous poly-glutamine deletion in USF3 may be involved in predisposition to heritable and sporadic epithelial thyroid carcinoma

artículo científico publicado en 2016

Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells

artículo científico publicado en 2016

Largescale population genomics versus deep phenotyping: Brute force or elegant pragmatism towards precision medicine

artículo científico publicado en 2019

Lucking into science.

artículo científico publicado en 2017

Molecular diagnosis of cutaneous leishmaniasis and species identification: analysis of 122 biopsies with varied parasite index.

artículo científico publicado en 2012

Non-canonical role of cancer-associated mutant SEC23B in the ribosome biogenesis pathway

scholarly article by Lamis Yehia published in September 2018

PTEN-opathies: from biological insights to evidence-based precision medicine

scientific article published on 07 January 2019

Preliminary report: Late seizure recurrence years after epilepsy surgery may be associated with alterations in brain tissue transcriptome.

artículo científico publicado en 2018

Thyroglobulin in Metastatic Thyroid Cancer: Culprit or Red Herring?

artículo científico publicado en 2017

Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations.

artículo científico publicado en 2018

Verbal memory dysfunction is associated with alterations in brain transcriptome in dominant temporal lobe epilepsy

scientific article published on 18 September 2020

Lista de obras de Lamis Yehia

A Nonpump Function of Sodium Iodide Symporter in Thyroid Cancer via Cross-talk with PTEN Signaling

Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors

Distinct Alterations in Tricarboxylic Acid Cycle Metabolites Associate with Cancer and Autism Phenotypes in Cowden Syndrome and Bannayan-Riley-Ruvalcaba Syndrome

Epidermal growth factor receptor and KRAS mutations in lung adenocarcinoma: a retrospective study of the Lebanese population.

Exome Sequencing Reveals Germline SMAD9 Mutation That Reduces Phosphatase and Tensin Homolog Expression and Is Associated With Hamartomatous Polyposis and Gastrointestinal Ganglioneuromas.

Exome sequencing reveals germline gain-of-function EGFR mutation in an adult with Lhermitte-Duclos disease.

Expression of HIF-1α and Markers of Angiogenesis Are Not Significantly Different in Triple Negative Breast Cancer Compared to Other Breast Cancer Molecular Subtypes: Implications for Future Therapy

Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer

Germline TTN variants are enriched in PTEN-wildtype Bannayan-Riley-Ruvalcaba syndrome.

Germline compound heterozygous poly-glutamine deletion in USF3 may be involved in predisposition to heritable and sporadic epithelial thyroid carcinoma

Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells

Largescale population genomics versus deep phenotyping: Brute force or elegant pragmatism towards precision medicine

Lucking into science.

Molecular diagnosis of cutaneous leishmaniasis and species identification: analysis of 122 biopsies with varied parasite index.

Non-canonical role of cancer-associated mutant SEC23B in the ribosome biogenesis pathway

PTEN-opathies: from biological insights to evidence-based precision medicine

Preliminary report: Late seizure recurrence years after epilepsy surgery may be associated with alterations in brain tissue transcriptome.

Thyroglobulin in Metastatic Thyroid Cancer: Culprit or Red Herring?

Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations.

Verbal memory dysfunction is associated with alterations in brain transcriptome in dominant temporal lobe epilepsy