T. Shahani

发表

Mosaic trisomy 22 in a 4‐year‐old boy with congenital heart disease and general hypotrophy: A case report

Z. Razavi, M. Maleki, N. Mahdieh, 2018, Journal of clinical laboratory analysis.

Patients With Invasive Ductal Carcinoma Have Reduced Levels of Decorin Expression in Their Breast Tissue Compared to Patients With Fibroadenoma While Plasma Decorin Remains Unchanged.

A. Jalilvand, A. Biglari, S. Mazloomzadeh, 2018, Archives of Iranian medicine.

Whole Exome Sequencing Revealed a Novel GJB1 Pathogenic Variant and a Rare BSCL2 Mutation in Two Iranian Large Pedigrees with Multiple Affected Cases of Charcot-Marie-Tooth

Hassan Rokni-Zadeh, A. Biglari, M. Maghbooli, 2019, International journal of molecular and cellular medicine.

A novel homozygous LRRK1 stop gain mutation in a patient suspected with osteosclerotic metaphyseal dysplasia

M. Miryounesi, Hassan Rokni-Zadeh, M. Shahrooei, 2020, Annals of human genetics.

While Urine and Plasma Decorin Remain Unchanged in Prostate Cancer, Prostatic Tissue Decorin Has a Prognostic Value.

M. Moghimi, M. Ayati, A. Biglari, 2020, Iranian biomedical journal.

Activation of human endothelial cells from specific vascular beds induces the release of a FVIII storage pool.

A. Luttun, K. Peerlinck, J. Saint-Remy, 2010, Blood.

Human liver sinusoidal endothelial cells but not hepatocytes contain factor VIII

K. Peerlinck, M. Jacquemin, E. Sokal, 2014, Journal of thrombosis and haemostasis : JTH.

Pro‐haemostatic effect of DDAVP is partially derived through non‐classical (CD14dim /CD16 ++) monocytes residing the spleen

M. Karimi, M. Jacquemin, Hassan Rokni-Zadeh, 2022, Journal of cellular and molecular medicine.

KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole.

P. Ray, M. Totonchi, Navid Almadani, 2021, European journal of obstetrics, gynecology, and reproductive biology.

Whole exome sequencing identifies both nuclear and mitochondrial variations in an Iranian family with non-syndromic hearing loss.

Hassan Rokni-Zadeh, A. Biglari, M. Shahrooei, 2019, Mitochondrion.

Pure ultra-fine carbon particles do not exert pro-coagulation and inflammatory effects on microvascular endothelial cells

M. Hoylaerts, M. Jacquemin, A. Biglari, 2018, Environmental Science and Pollution Research.

Extensive genetic screening of Iranian Factor FVII-deficient individuals unraveled several novel mutations and postulated founder effects in some cases

Hassan Rokni-Zadeh, S. Ravanbod, T. Shahani, 2022, Research and practice in thrombosis and haemostasis.

Exome-first Approach Identified Novel Homozygous Dedicator of Cytokinesis 8 (DOCK8) Mutations in Three Unrelated Iranian Pedigrees Suspected with Hyper-IgE Syndrome.

X. Bossuyt, S. Alyasin, Hassan Rokni-Zadeh, 2020, Iranian journal of allergy, asthma, and immunology.

GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co‐occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart disease

M. Maleki, N. Mahdieh, Hassan Rokni-Zadeh, 2019, Journal of clinical laboratory analysis.

Non-viral Suicide Gene Therapy: Cytosine Deaminase Gene Directed by VEGF Promoter and 5-fluorocytosine as a Gene Directed Enzyme/prodrug System in Breast Cancer Model

A. Abbaspour, A. Sharafi, A. Biglari, 2021, Drug Research.