Variation of Nanostructures, Molecular Interactions, and Anisotropic Elastic Moduli of Lignocellulosic Cell Walls with Moisture by S. Youssefian, J. E. Jakes, N. Rahbar

Get full text

P244: DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity by Hassan Vahidnezhad, Amir Hozhabrpour, Leila Youssefian, Fatemeh Vahidnezhad

Get full text

Reduced pain sensitivity of episodic pain syndrome model mice carrying a Nav1.9 mutation by ANP-230, a novel sodium channel blocker by Hiroko Okuda, Sumiko Inoue, Yoshihiro Oyamada, Akio Koizumi, Shohab Youssefian

Get full text

Epidermolysis bullosa and the COVID-19 pandemic: challenges and recommendations by Hassan Vahidnezhad, Hamideh Moravvej, Ayda Bahmanjahromi, Leila Youssefian, Fahimeh Abdollahimajd

Get full text

P756: Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review by Leila Youssefian, Sajjad Biglari, Atefeh Sohanforooshan Moghaddam, Amir Hossein Saeidian, Fatemeh Vahidnezhad, Hassan Vahidnezhad

Get full text

P671: Whole-transcriptome-based skin virome profiling in typical epidermodysplasia verruciformis patients reveals infections with α-, β- and γ-HPVs by Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, Jouni Uitto, Fatemeh Vahidnezhad, Zahra Saffarian, Niloofar Faraji

Get full text

Hypotrichosis with juvenile macular dystrophy: Combination of whole‐genome sequencing and genome‐wide homozygosity mapping identifies a large deletion in CDH3 initially undetected... by Amir Hossein Saeidian, Hassan Vahidnezhad, Leila Youssefian, Soheila Sotudeh, Meisam Sargazi, Sirous Zeinali, Jouni Uitto

Get full text

Autozygosity Mapping by Genome-wide Single Nucleotide Polymorphism Array Identifies a Novel Homozygous HR Mutation in a Consanguineous Family with Universal Hereditary Hair Loss by Sirous Zeinali, Leila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, Soheila Sotoudeh, Hamideh Bagherian, Jouni Uitto

Get full text

A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome by Leila Youssefian, Andrew Touati, Amir Hossein Saeidian, Omid Zargari, Sirous Zeinali, Hassan Vahidnezhad, Jouni Uitto

Get full text

Deletion of 2 amino acids in IHH in a Japanese family with brachydactyly type A1 by Nozomu Ozaki, Hiroko Okuda, Hatasu Kobayashi, Kouji H. Harada, Sumiko Inoue, Shohab Youssefian, Akio Koizumi

Get full text

The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series by Leila Youssefian, Hassan Vahidnezhad, Andrew Touati, Vahid Ziaee, Amir Hossein Saeidian, Sara Pajouhanfar, Sirous Zeinali, Jouni Uitto

Get full text

Reverse pneumatic artificial muscles (rPAMs): Modeling, integration, and control. by Erik H Skorina, Ming Luo, Wut Yee Oo, Weijia Tao, Fuchen Chen, Sina Youssefian, Nima Rahbar, Cagdas D Onal

Get full text

Lipoid Proteinosis Due to Homozygous Deletion Mutation (c.735delTG) in the ECM1 Gene Presents with Seizures and Hoarseness but No Skin Involvement by Hassan Vahidnezhad, Leila Youssefian, Abbas Tafakhori, Qiaoli Li, Jouni Uitto, Fatemeh Vand Rajabpour, Morteza Pishnamazi, Amirhossein Modabbernia, Mina Tabrizi

Get full text

Genetic Predisposition to Numerous Large Ulcerating Basal Cell Carcinomas and Response to Immune Therapy by Bahar Dasgeb, Youssefian Leila, Amir Hossein Saeidian, Jun Kang, Wenyin Shi, Elizabeth Shoenberg, Adam Ertel, Paolo Fortina, Hassan Vahidnezhad, Jouni Uitto

Get full text

P366: Loss-of-function EGFR mutation in Bartter syndrome with neonatal epithelial autoinflammation by Leila Youssefian, Hassan Vahidnezhad, Jouni Uitto, Amir Hossein Saeidian, Rana Samii, Elnaz Kalamati, Ali Reza Tavasoli, Zahra Saffarian, John A. McGrath, Soheila Sotoudeh

Get full text

Three-window ultrasonography confirmation of endotracheal tube placement by Shadi Lahham, Sean P Wilson, Elizabeth Turner, Mohammad Subeh, Mark A Rosen, Arthur Youssefian, Craig L Anderson, Melika Hosseini, Sasha Rosen, Abdulatif Gari, John C Fox

Get full text

ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification. by Douglas Ralph, Yvonne Nitschke, Michael A Levine, Matthew Caffet, Tamara Wurst, Amir Hossein Saeidian, Leila Youssefian, Hassan Vahidnezhad, Sharon F Terry, Frank Rutsch, Jouni Uitto, Qiaoli Li

Get full text

Rare variants in , a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia-induced pulmonary hyperte... by Hatasu Kobayashi, Risako Kabata, Hideyuki Kinoshita, Takaaki Morimoto, Koh Ono, Midori Takeda, Jungmi Choi, Hiroko Okuda, Wanyang Liu, Kouji H. Harada, Takeshi Kimura, Shohab Youssefian, Akio Koizumi

Get full text

Finite Element-Based Personalized Simulation of Duodenal Hydrogel Spacer: Spacer Location Dependent Duodenal Sparing and a Decision Support System for Spacer-Enabled Pancreatic Can... by Hamed Hooshangnejad, Hamed Hooshangnejad, Sina Youssefian, Amol Narang, Eun Ji Shin, Avani Dholakia Rao, Sarah Han-Oh, Todd McNutt, Junghoon Lee, Chen Hu, John Wong, Kai Ding

Get full text

Circumvention of Mcl-1-dependent drug resistance by simultaneous Chk1 and MEK1/2 inhibition in human multiple myeloma cells. by Xin-Yan Pei, Yun Dai, Jessica Felthousen, Shuang Chen, Yukie Takabatake, Liang Zhou, Leena E Youssefian, Michael W Sanderson, Wesley W Bodie, Lora B Kramer, Robert Z Orlowski, Steven Grant

Get full text