Molecular Origin of Strength and Stiffness in Bamboo Fibrils

por Youssefian, Sina, Rahbar, Nima
Publicado 2015

Variation of Nanostructures, Molecular Interactions, and Anisotropic Elastic Moduli of Lignocellulosic Cell Walls with Moisture

por Youssefian, S., Jakes, J. E., Rahbar, N.
Publicado 2017

Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis

por UITTO, Jouni, YOUSSEFIAN, Leila, SAEIDIAN, Amir Hossein, VAHIDNEZHAD, Hassan
Publicado 2020

Reduced pain sensitivity of episodic pain syndrome model mice carrying a Nav1.9 mutation by ANP-230, a novel sodium channel blocker

por Okuda, Hiroko, Inoue, Sumiko, Oyamada, Yoshihiro, Koizumi, Akio, Youssefian, Shohab
Publicado 2023

Variation of thermal conductivity of DPPC lipid bilayer membranes around the phase transition temperature

por Youssefian, Sina, Rahbar, Nima, Lambert, Christopher R., Van Dessel, Steven
Publicado 2017

Mechanical allodynia triggered by cold exposure in mice with the Scn11a p.R222S mutation: a novel model of drug therapy for neuropathic pain related to Na(V)1.9

por Matsubara, Yosuke, Okuda, Hiroko, Harada, Kouji H., Youssefian, Shohab, Koizumi, Akio
Publicado 2020

A new horizon of moyamoya disease and associated health risks explored through RNF213

por Koizumi, Akio, Kobayashi, Hatasu, Hitomi, Toshiaki, Harada, Kouji H., Habu, Toshiyuki, Youssefian, Shohab
Publicado 2015

Nodular osteochondrogenic activity in soft tissue surrounding osteoma in neurogenic para osteo-arthropathy: morphological and immunohistochemical study

por Youssefian, T, Sapena, R, Carlier, R, Bos, C, Denormandie, A, Denys, P, Cormier, A, Bandelier, M
Publicado 2004

A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome

por Youssefian, Leila, Touati, Andrew, Saeidian, Amir Hossein, Zargari, Omid, Zeinali, Sirous, Vahidnezhad, Hassan, Uitto, Jouni
Publicado 2017

Hypotrichosis with juvenile macular dystrophy: Combination of whole‐genome sequencing and genome‐wide homozygosity mapping identifies a large deletion in CDH3 initially undetected...

por Saeidian, Amir Hossein, Vahidnezhad, Hassan, Youssefian, Leila, Sotudeh, Soheila, Sargazi, Meisam, Zeinali, Sirous, Uitto, Jouni
Publicado 2019

Deletion of 2 amino acids in IHH in a Japanese family with brachydactyly type A1

por Ozaki, Nozomu, Okuda, Hiroko, Kobayashi, Hatasu, Harada, Kouji H., Inoue, Sumiko, Youssefian, Shohab, Koizumi, Akio
Publicado 2021

The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series

por Youssefian, Leila, Vahidnezhad, Hassan, Touati, Andrew, Ziaee, Vahid, Saeidian, Amir Hossein, Pajouhanfar, Sara, Zeinali, Sirous, Uitto, Jouni
Publicado 2018

Rice DEP1, encoding a highly cysteine-rich G protein γ subunit, confers cadmium tolerance on yeast cells and plants

por Kunihiro, Shuta, Saito, Tatsuhiko, Matsuda, Taiki, Inoue, Masataka, Kuramata, Masato, Taguchi-Shiobara, Fumio, Youssefian, Shohab, Berberich, Thomas, Kusano, Tomonobu
Publicado 2013

Reverse pneumatic artificial muscles (rPAMs): Modeling, integration, and control

por Skorina, Erik H., Luo, Ming, Oo, Wut Yee, Tao, Weijia, Chen, Fuchen, Youssefian, Sina, Rahbar, Nima, Onal, Cagdas D.
Publicado 2018

Genetic Predisposition to Numerous Large Ulcerating Basal Cell Carcinomas and Response to Immune Therapy

por Dasgeb, Bahar, Leila, Youssefian, Saeidian, Amir Hossein, Kang, Jun, Shi, Wenyin, Shoenberg, Elizabeth, Ertel, Adam, Fortina, Paolo, Vahidnezhad, Hassan, Uitto, Jouni
Publicado 2021

β-cell-specific overexpression of adiponectin receptor 1 does not improve diabetes mellitus in Akita mice

por Choi, Jungmi, Kobayashi, Hatasu, Okuda, Hiroko, Harada, Kouji H., Takeda, Midori, Fujimoto, Hiroyuki, Yamane, Shunsuke, Tanaka, Daisuke, Youssefian, Shohab, Inagaki, Nobuya, Koizumi, Akio
Publicado 2018

Finite Element-Based Personalized Simulation of Duodenal Hydrogel Spacer: Spacer Location Dependent Duodenal Sparing and a Decision Support System for Spacer-Enabled Pancreatic Can...

por Hooshangnejad, Hamed, Youssefian, Sina, Narang, Amol, Shin, Eun Ji, Rao, Avani Dholakia, Han-Oh, Sarah, McNutt, Todd, Lee, Junghoon, Hu, Chen, Wong, John, Ding, Kai
Publicado 2022

Rare variants in RNF213, a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia-induced pulmonary hypertension in mice

por Kobayashi, Hatasu, Kabata, Risako, Kinoshita, Hideyuki, Morimoto, Takaaki, Ono, Koh, Takeda, Midori, Choi, Jungmi, Okuda, Hiroko, Liu, Wanyang, Harada, Kouji H., Kimura, Takeshi, Youssefian, Shohab, Koizumi, Akio
Publicado 2018

ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification

por Ralph, Douglas, Nitschke, Yvonne, Levine, Michael A., Caffet, Matthew, Wurst, Tamara, Saeidian, Amir Hossein, Youssefian, Leila, Vahidnezhad, Hassan, Terry, Sharon F., Rutsch, Frank, Uitto, Jouni, Li, Qiaoli
Publicado 2022

Circumvention of Mcl-1-Dependent Drug Resistance by Simultaneous Chk1 and MEK1/2 Inhibition in Human Multiple Myeloma Cells

por Pei, Xin-Yan, Dai, Yun, Felthousen, Jessica, Chen, Shuang, Takabatake, Yukie, Zhou, Liang, Youssefian, Leena E., Sanderson, Michael W., Bodie, Wesley W., Kramer, Lora B., Orlowski, Robert Z., Grant, Steven
Publicado 2014