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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Disease and RBPJ[original query]
Functional genomics identifies negative regulatory nodes controlling phagocyte oxidative burst.
Nature communications 2015 6 7838.
Graham Daniel B, Becker Christine E, Doan Aivi, Goel Gautam, Villablanca Eduardo J, Knights Dan, Mok Amanda, Ng Aylwin C Y, Doench John G, Root David E, Clish Clary B, Xavier Ramnik
RBPJ polymorphisms associated with cerebral infarction diseases in Chinese Han population: A Clinical Trial/Experimental Study (CONSORT Compliant).
Medicine 2018 Aug 97 (31): e11420.
Zhang Qiong, Zhou Jie, Lei Hong, Zhu Chun-Yu, Li Fei-Feng, Zheng Dong, Liu Shu-L
High-throughput identification of noncoding functional SNPs via type IIS enzyme restriction.
Nature genetics 2018 7 50 (8): 1180-1188.
Li Gang, Martínez-Bonet Marta, Wu Di, Yang Yu, Cui Jing, Nguyen Hung N, Cunin Pierre, Levescot Anaïs, Bai Ming, Westra Harm-Jan, Okada Yukinori, Brenner Michael B, Raychaudhuri Soumya, Hendrickson Eric A, Maas Richard L, Nigrovic Peter
Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort.
Human mutation 2018 Jun .
Meester Josephina A N, Sukalo Maja, Schröder Kim C, Schanze Denny, Baynam Gareth, Borck Guntram, Bramswig Nuria C, Duman Duygu, Gilbert-Dussardier Brigitte, Holder-Espinasse Muriel, Itin Peter, Johnson Diana S, Joss Shelagh, Koillinen Hannele, McKenzie Fiona, Morton Jenny, Nelle Heike, Reardon Willie, Roll Claudia, Salih Mustafa A, Savarirayan Ravi, Scurr Ingrid, Splitt Miranda, Thompson Elizabeth, Titheradge Hannah, Travers Colm P, Van Maldergem Lionel, Whiteford Margo, Wieczorek Dagmar, Vandeweyer Geert, Trembath Richard, Van Laer Lut, Loeys Bart L, Zenker Martin, Southgate Laura, Wuyts W
Abnormal expression and mutation of the RBPJ gene may be involved in CD59 clonal proliferation in paroxysmal nocturnal hemoglobinuria.
Experimental and therapeutic medicine 2019 5 17 (6): 4536-4546.
Li Liyan, Liu Hui, Wang Honglei, Liu Zhaoyun, Chen Yingying, Li Lijuan, Song Jia, Wang Guojin, Fu Ro
Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseases.
PLoS genetics 2020 1 16 (1): e1008538.
Nurnberg Sylvia T, Guerraty Marie A, Wirka Robert C, Rao H Shanker, Pjanic Milos, Norton Scott, Serrano Felipe, Perisic Ljubica, Elwyn Susannah, Pluta John, Zhao Wei, Testa Stephanie, Park YoSon, Nguyen Trieu, Ko Yi-An, Wang Ting, Hedin Ulf, Sinha Sanjay, Barash Yoseph, Brown Christopher D, Quertermous Thomas, Rader Daniel
Association of a Functional Single Nucleotide Polymorphism (rs874040) in the RBPJ Gene with Susceptibility to Rheumatoid Arthritis in Iranian Population.
Avicenna journal of medical biotechnology 2021 9 13 (3): 166-170.
Salesi Mansour, Oboodiyat Mahdieh, Salehi Rasoul, Pakzad Bahr
Alpha synuclein (SNCA) rs7684318 variant contributes to Parkinson's disease risk by altering transcription factor binding related with Notch and Wnt signaling.
Neuroscience letters 2021 04 750 135802.
Naushad Shaik Mohammad, Hussain Tajamul, Alrokayan Salman, Kutala Vijay Kum
Identification of tumour antigens and immune subtypes in the development of an anti-cancer vaccine for endometrial carcinoma.
Scandinavian journal of immunology 2022 12 97 (3): e13250.
Feng Jianyang, He Ho
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