日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Dissecting lncRNA-mRNA regulatory network in type 2 diabetes as the risk factor of pancreatic cancer

解析2型糖尿病中lncRNA-mRNA调控网络作为胰腺癌风险因素的作用

Nilchi, Amirhossein Naghsh; Dehghanian, Fariba; Vallian, Sadeq; Bahreini, Amin

Noncoding RNAs and DNA methylation as epigenetic modulators of breast cancer: mechanisms and clinical perspectives in the Iranian population, a systematic review

非编码RNA和DNA甲基化作为乳腺癌表观遗传调控因子:伊朗人群的机制和临床展望——系统综述

Mashayekh, Zeynab; Fard, Rasool Fatehi; Vallian, Sadeq

Molecular signatures of breast cancer in the Iranian population: a review of cell growth and cell cycle regulators

伊朗人群乳腺癌的分子特征:细胞生长和细胞周期调控因子的综述

Mashayekh, Zeynab; Broojeni, Jalal Vallian; Fard, Rasool Fatehi; Vallian, Sadeq

Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism

关键自噬锚定因子EPG5的突变与神经发育障碍和神经退行性疾病(包括早发性帕金森病)相关。

Dafsari, Hormos Salimi; Deneubourg, Celine; Singh, Kritarth; Maroofian, Reza; Suprenant, Zita; Kho, Ay Lin; Ingham, Neil J; Steel, Karen P; Sheshadri, Preethi; Baur, Franciska; Hentrich, Lea; Gerisch, Birgit; Zamani, Mina; Alves, Cesar; Siddiqui, Ata; Dafsari, Haidar S; Salari, Mehri; Lang, Anthony E; Harris, Michael; Abdelaleem, Alice; Sadeghian, Saeid; Azizimalamiri, Reza; Galehdari, Hamid; Shariati, Gholamreza; Sedaghat, Alireza; Zeighami, Jawaher; Calame, Daniel; Marafi, Dana; Duan, Ruizhi; Boehnke, Adrian; Clark, Gary D; Rosenfeld, Jill A; Mohila, Carrie A; Steel, Dora; Chopra, Saurabh; Sharma, Suvasini; Kohlschmidt, Nicolai; Patzer, Steffi; Saffari, Afshin; Ebrahimi-Fakhari, Darius; Çavdartepe, Büşra Eser; Chang, Irene J; Beckman, Erika; Peters, Renate; Fennell, Andrew Paul; Lo, Bernice; Averdunk, Luisa; Distelmaier, Felix; Baethmann, Martina; Elmslie, Frances; Joost, Kairit; Nampoothiri, Sheela; Yesodharan, Dhanya; Mandel, Hanna; Kimball, Amy; Kline, Antonie D; Mignot, Cyril; Keren, Boris; Laugel, Vincent; Õunap, Katrin; Devadathan, Kalpana; van Berkestijn, Frederique M C; Silwal, Arpana; Koene, Saskia; Verma, Sumit; Karim, Mohammed Yousuf; Boubidi, Chahynez; Aziz, Majid; ElGhazali, Gehad; Mattas, Lauren; Miryounesi, Mohammad; Hashemi-Gorji, Farzad; Alavi, Shahryar; Nouri, Nayereh; Noruzinia, Mehrdad; Kavousi, Saeideh; Kamath, Arveen; Jayawant, Sandeep; Saneto, Russell; Haridy, Nourelhoda A; Kart, Pinar Ozkan; Cansu, Ali; Joubert, Madeleine; Beneteau, Claire; Stuurman, Kyra E; Wilke, Martina; Barakat, Tahsin Stefan; Tajsharghi, Homa; Scardamaglia, Annarita; Vallian, Sadeq; Hız, Semra; Shoeibi, Ali; Boostani, Reza; Hashemi, Narges; Babaei, Meisam; Alsaleh, Norah Saleh; Porter, Julie; Attié-Bitach, Tania; Marzin, Pauline; Wicher, Dorota; Gold, Jessica I; Schuler, Elisabeth; Kashgari, Amna; Alanazi, Rakan F; Eyaid, Wafaa; Engelen, Marc; Langeveld, Mirjam; Stüve, Burkhard; Li, Yun; Yigit, Gökhan; Wollnik, Bernd; Monje, Mariana H G; Krainc, Dimitri; Mencacci, Niccolò E; Bakhtiari, Somayeh; Kruer, Michael; Argilli, Emanuela; Sherr, Elliott; Jamshidi, Yalda; Karimiani, Ehsan Ghayoor; Cheung, Yiu Wing Sunny; Karin, Ivan; Zifarelli, Giovanni; Bauer, Peter; Chung, Wendy K; Lupski, James R; Kurian, Manju A; Dötsch, Jörg; von Kleist-Retzow, Jürgen-Christoph; Klopstock, Thomas; Wagner, Matias; Yip, Calvin; Roos, Andreas; Carsetti, Rita; Dionisi-Vici, Carlo; Gautel, Mathias; Duchen, Michael R; Antebi, Adam; Houlden, Henry; Fanto, Manolis; Jungbluth, Heinz

Defects in meiosis I contribute to the genesis of androgenetic hydatidiform moles

减数分裂I缺陷是导致雄激素性葡萄胎发生的原因之一。

Rezaei, Maryam; Liang, Manqi; Yalcin, Zeynep; Martin, Jacinta H; Kazemi, Parinaz; Bareke, Eric; Ge, Zhao-Jia; Fardaei, Majid; Benadiva, Claudio; Hemida, Reda; Hassan, Adnan; Maher, Geoffrey J; Abdalla, Ebtesam; Buckett, William; Bolze, Pierre-Adrien; Sandhu, Iqbaljit; Duman, Onur; Agrawal, Suraksha; Qian, JianHua; Vallian Broojeni, Jalal; Bhati, Lavi; Miron, Pierre; Allias, Fabienne; Selim, Amal; Fisher, Rosemary A; Seckl, Michael J; Sauthier, Philippe; Touitou, Isabelle; Tan, Seang Lin; Majewski, Jacek; Taketo, Teruko; Slim, Rima

Author Correction: Identification of ITPR1 gene as a novel target for hsa-miR-34b-5p in non-obstructive azoospermia: a Ca(2+)/apoptosis pathway cross-talk

作者更正:鉴定 ITPR1 基因为非梗阻性无精子症中 hsa-miR-34b-5p 的新靶点:Ca(2+)/细胞凋亡通路交叉对话

Maleki, Bahareh; Modarres, Parastoo; Salehi, Peyman; Vallian, Sadeq

Identification of ITPR1 gene as a novel target for hsa-miR-34b-5p in non-obstructive azoospermia: a Ca2+/apoptosis pathway cross-talk

在非梗阻性无精子症中,ITPR1基因被鉴定为hsa-miR-34b-5p的新靶点:Ca2+/细胞凋亡通路交叉对话

Bahareh Maleki ,Parastoo Modarres ,Peyman Salehi ,Sadeq Vallian

Exome sequencing identifies novel variants associated with non-syndromic hearing loss in the Iranian population

外显子组测序发现了与伊朗人群非综合征性听力损失相关的新变异

Jalal Vallian Broojeni, Arezu Kazemi, Halimeh Rezaei, Sadeq Vallian

LncRNA LOC100507144 acts as a novel regulator of CD44/Nanog/Sox2/miR-302/miR-21 axis in colorectal cancer

LncRNA LOC100507144 作为结直肠癌中 CD44/Nanog/Sox2/miR-302/miR-21 轴的新型调节剂

Nasim Ebrahimi, Hajar Rezanejad, Malek Hossein Asadi, Sadeq Vallian

A recurrent homozygous missense DPM3 variant leads to muscle and brain disease

一种复发的纯合错义DPM3变异会导致肌肉和脑部疾病

Nagy, Sara; Lau, Tracy; Alavi, Shahryar; Karimiani, Ehsan Ghayoor; Vallian, Jalal; Ng, Bobby G; Noroozi Asl, Samaneh; Akhondian, Javad; Bahreini, Amir; Yaghini, Omid; Uapinyoying, Prech; Bonnemann, Carsten; Freeze, Hudson H; Dissanayake, Vajira H W; Sirisena, Nirmala D; Schmidts, Miriam; Houlden, Henry; Moreno-De-Luca, Andres; Maroofian, Reza