Search Results - "genomic imprinting"

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  1. 21
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    Regulatory role of long non coding RNAs (lncRNAs) in neurological disorders: From novel biomarkers to promising therapeutic strategies by Nirjhar Bhattacharyya, Vedansh Pandey, Malini Bhattacharyya, Abhijit Dey

    Published 2021
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  2. 22
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    Neocortical development as an evolutionary platform for intragenomic conflict by Eric eLewitus, Alex T. Kalinka

    Published 2013
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  3. 23
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    Adenovirus-mediated gene delivery restores fertility in congenitally infertile female mice by Mito KANATSU-SHINOHARA, Jiyoung LEE, Takehiro MIYAZAKI, Hiroko MORIMOTO, Takashi SHINOHARA

    Published 2022
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  4. 24
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    Genetic syndromes associated with overgrowth in childhood by Jung Min Ko

    Published 2013
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  5. 25
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    COMPREHENSIVE TREATMENT OF CHILDREN AND ADOLESCENTS WITH PRADER-WILLI SYNDROME AT CENTRE FOR EDUCATION, REHABILITATION, AND TRAINING CIRIUS KAMNIK by Tina Bregant, Marta Orehek Kirbiš, Teja Bandel-Castro, Andreja Širca Čampa, Primož Kotnik

    Published 2024
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  6. 26
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    Anesthetic care during posterior spinal fusion in a patient with Prader-Willi syndrome. by N. Rusin, J. D. Tobias

    Published 2020
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  7. 27
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    Systematic review of the clinical and genetic aspects of Prader-Willi syndrome by Dong Kyu Jin

    Published 2011
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  8. 28
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    A Korean Child with Schaaf-Yang Syndrome Presented with Hearing Impairment: A Case Report by Seung Hoon Lee, Seung Han Shin, Jung Min Ko, Boram Kim, Hyeon Sae Oh, Man Jin Kim, Seul Gi Park, Ee-Kyung Kim, Han-Suk Kim

    Published 2022
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  9. 29
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    The effect of valproic acid on intrinsic, extrinsic, and JAK/STAT pathways in neuroblastoma and glioblastoma cell lines by Masumeh Sanaei, Fraidoon Kavoosi

    Published 2022
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  10. 30
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    High-throughput detection of aberrant imprint methylation in the ovarian cancer by the bisulphite PCR-Luminex method by Hiura Hitoshi, Okae Hiroaki, Kobayash Hisato, Miyauchi Naoko, Sato Fumi, Sato Akiko, Suzuki Fumihiko, Nagase Satoru, Sugawara Junichi, Nakai Kunihiko, Yaegashi Nobuo, Arima Takahiro

    Published 2012
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  11. 31
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    Influence of conception and delivery mode on stress response marker Oct4B1 and imprinted gene expression related to embryo development: A cohort study by Maria Argyraki, Socrates Katafigiotis, Theofanis Vavilis, Zoe Papadopoulou, Giorgos Tzimagiorgis, Anna-Bettina Haidich, Katerina Chatzimeletiou, Grigoris Grimbizis, Basil Tarlatzis, Maria Syrrou, Alexandros Lambropoulos

    Published 2021
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  12. 32
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    Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature by Cinthia Aguilera, Marina Viñas-Jornet, Neus Baena, Elisabeth Gabau, Concepción Fernández, Nuria Capdevila, Sanja Cirkovic, Adrijan Sarajlija, Marijana Miskovic, Danijela Radivojevic, Anna Ruiz, Miriam Guitart

    Published 2017
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  13. 33
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    The role of epigenetics in male and female infertility by D. A. Egorova, V. V. Derezina, M. V. Chebanyan, M. B. Sultonova, T. V. Ishmuratov, M. M. Gasanov, A. Z. Chipchikova, S. A. Paksileva, S. S. Mitkina, R. R. Khamidullina, A. Sh. Kutueva, A. A. Anikeeva

    Published 2024
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  14. 34
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    No influence of parental origin of intact X chromosome and/or Y chromosome sequences on three-year height response to growth hormone therapy in Turner syndrome by Hye Jin Lee, Hae Woon Jung, Gyung Min Lee, Hwa Young Kim, Jae Hyun Kim, Sun Hee Lee, Ji Hyun Kim, Young Ah Lee, Choong Ho Shin, Sei Won Yang

    Published 2014
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  15. 35
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    Off to a good start: environmental imprinting in the childbirth period by Antonio Ragusa, Simone Rugolotto, Sara D'Avino, Chiara Incarnato, Alessandra Meloni, Alessandro Svelato

    Published 2019
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  16. 36
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    El tumor de Wilms. Un paradigma de heterogeneidad genética: a paradigm of genetic heterogeneity Wilm's toumor by Rolando A Hernández Fernández

    Published 2011
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  17. 37
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    Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases by Maria Francesca Bedeschi, Mariarosaria Calvello, Leda Paganini, Lidia Pezzani, Marco Baccarin, Laura Fontana, Silvia M. Sirchia, Silvana Guerneri, Lorena Canazza, Ernesto Leva, Lorenzo Colombo, Faustina Lalatta, Fabio Mosca, Silvia Tabano, Monica Miozzo

    Published 2017
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  18. 38
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    Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report by Caroline Lekszas, Indrajit Nanda, Barbara Vona, Julia Böck, Farah Ashrafzadeh, Nahid Donyadideh, Farnoosh Ebrahimzadeh, Najmeh Ahangari, Reza Maroofian, Ehsan Ghayoor Karimiani, Thomas Haaf

    Published 2019
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  19. 39
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    The effect of growth hormone on the metabolome of follicular fluid in patients with diminished ovarian reserve by Fan He, Fang Wang, Yang Yang, Zhi Yuan, Chengguang Sun, Heng Zou, Huijia Chen, Hongliang Yi, Shan Hu Gao, Shen Zhang, Lina Hu, Ting-li Han

    Published 2023
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  20. 40
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    Aberrant DNA methylation associated with the development of metabolic dysfunction-associated fatty liver disease by O.E. Abaturov, A.O. Nikulina, O.O. Rusakova

    Published 2024
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