Rapid methodologies for assessing Pseudomonas syringae pv. actinidiae colonization and effector-mediated hypersensitive response in kiwifruit
Jayaraman, Jay, Chatterjee, Abhishek, Hunter, Shannon, Chen, Ronan, Stroud, Erin A, Saei, Hassan, Hoyte, Stephen, Deroles, Simon, Tahir, Jibran, Templeton, Matthew D, Brendolise, Cyril
Published in Molecular plant-microbe interactions (01.08.2021)
Published in Molecular plant-microbe interactions (01.08.2021)
Get full text
Journal Article
Whole-Exome Sequencing Uncovers Novel Causative Variants and Additional Findings in Three Patients Affected by Glycogen Storage Disease Type VI and Fanconi-Bickel Syndrome
Eghbali, Maryam, Fatemi, Kiyana Sadat, Salehpour, Shadab, Abiri, Maryam, Saei, Hassan, Talebi, Saeed, Olyaei, Nasrin Alipour, Yassaee, Vahid Reza, Modarressi, Mohammad Hossein
Published in Frontiers in genetics (11.01.2021)
Published in Frontiers in genetics (11.01.2021)
Get full text
Journal Article
VNtyper enables accurate alignment-free genotyping of MUC1 coding VNTR using short-read sequencing data in autosomal dominant tubulointerstitial kidney disease
Saei, Hassan, Morinière, Vincent, Heidet, Laurence, Gribouval, Olivier, Lebbah, Said, Tores, Frederic, Mautret-Godefroy, Manon, Knebelmann, Bertrand, Burtey, Stéphane, Vuiblet, Vincent, Antignac, Corinne, Nitschké, Patrick, Dorval, Guillaume
Published in iScience (21.07.2023)
Published in iScience (21.07.2023)
Get full text
Journal Article
P135: X-linked Alport syndrome: From transcriptomic diagnosis to preclinical assessment of splice-switching oligonucleotide therapy using patient-derived cells and kidney organoids
Saei, Hassan, Boisson, Marie, Arrondel, Christelle, Estebe, Bruno, Cagnard, Nicolas, Bras, Marc, Morinière, Vincent, Arkoub, Zaïna Aït, Heidet, Laurence, Gribouval, Olivier, Nitschké, Patrick, Antignac, Corinne, Mollet, Géraldine, Dorval, Guillaume
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
Get full text
Journal Article
P168: MUC1 gene coding-VNTR alignment-free genotyping approach augmented ADTKD diagnosis in a cohort of 3735 patients with hereditary kidney diseases
Saei, Hassan, Kachmar, Jessica, Morinière, Vincent, Heidet, Laurence, Gribouval, Olivier, Lebbah, Said, Tores, Frederic, Mautret-Godefroy, Manon, Knebelmann, Bertrand, Burtey, Stéphane, Vuiblet, Vincent, Antignac, Corinne, Nitschké, Patrick, Dorval, Guillaume
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
Get full text
Journal Article
2606 Clinically boosted exome-sequencing is necessary for accurate and highly sensitive genetic diagnosis of ADTKD-MUC1
Saei, Hassan, Morinière, Vincent, Heidet, Laurence, Knebelmann, Bertrand, Nitschke, Patrick, Antignac, Corinne, Dorval, Guillaume
Published in Nephrology, dialysis, transplantation (23.05.2024)
Published in Nephrology, dialysis, transplantation (23.05.2024)
Get full text
Journal Article
Identification of a novel mutation in the HACD1 gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportion
Jabbarpour, Neda, Poorshiri, Bita, Saei, Hassan, Barzegar, Mohammad, Bonyadi, Mortaza
Published in Journal of genetics (24.01.2023)
Published in Journal of genetics (24.01.2023)
Get full text
Journal Article
382 Unexpected diagnoses of ADTKD-MUC1 with the help of VNtyper
Kachmar, Jessica, Saei, Hassan, Morinière, Vincent, Heidet, Laurence, Gribouval, Olivier, Mautret-Godefroy, Manon, Knebelmann, Bertrand, Burtey, Stéphane, Vuiblet, Vincent, Nitschké, Patrick, Antignac, Corinne, Dorval, Guillaume
Published in Nephrology, dialysis, transplantation (23.05.2024)
Published in Nephrology, dialysis, transplantation (23.05.2024)
Get full text
Journal Article
Identification of novel cis-mutations in the GJA8 gene in a 3-generation Iranian family with autosomal dominant congenital nuclear cataract
Jabbarpour, Neda, Saei, Hassan, Jabbarpoor Bonyadi, Mohammad Hossein, Bonyadi, Mortaza
Published in Ophthalmic genetics (03.09.2022)
Published in Ophthalmic genetics (03.09.2022)
Get full text
Journal Article
Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations
Abiri, Maryam, Saei, Hassan, Eghbali, Maryam, Karamzadeh, Razieh, Shirzadeh, Tina, Sharifi, Zohreh, Zeinali, Sirous
Published in Metabolic brain disease (01.08.2019)
Published in Metabolic brain disease (01.08.2019)
Get full text
Journal Article
A wave of deep intronic mutations in X-linked Alport syndrome
Boisson, Marie, Arrondel, Christelle, Cagnard, Nicolas, Morinière, Vincent, Arkoub, Zaïna Aït, Saei, Hassan, Heidet, Laurence, Kachmar, Jessica, Hummel, Aurélie, Knebelmann, Bertrand, Bonnet-Dupeyron, Marie-Noëlle, Isidor, Bertrand, Izzedine, Hassane, Legrand, Eric, Couarch, Philippe, Gribouval, Olivier, Bole-Feysot, Christine, Parisot, Mélanie, Nitschké, Patrick, Antignac, Corinne, Dorval, Guillaume
Published in Kidney international (01.08.2023)
Published in Kidney international (01.08.2023)
Get full text
Journal Article
The Effect of Alginate-Based Edible Coating Enriched with Citric Acid and Ascorbic Acid on Texture, Appearance and Eating Quality of Apple Fresh-Cut
Najafi Marghmaleki, Solaleh, Mortazavi, Seyed Mohammad Hassan, Saei, Hassan, Mostaan, Ahmad
Published in International journal of fruit science (01.01.2021)
Published in International journal of fruit science (01.01.2021)
Get full text
Journal Article
Hepatoprotective Effect of Ethanolic Extract of Lavandula officinalis L. in Alloxan-Induced Diabetic Rats
Saei, Hassan, Azarmi, Mehrdad, Dehghan, Gholamreza, Zehtab Salmasi, Said, Zeinali, Sevda
Published in Thrita (10.05.2016)
Published in Thrita (10.05.2016)
Get full text
Journal Article