CCDC55 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "CCDC55" in English language version.

refsWebsite

Global rank English rank

13nih.gov

4^th place

5doi.org

2^nd place

4worldcat.org

5^th place

2ensembl.org

1,626^th place

1,007^th place

1omim.org

4,380^th place

4,305^th place

doi.org

Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, Bocher M, Blocker H, Bauersachs S, Blum H, Lauber J, Dusterhoft A, Beyer A, Kohrer K, Strack N, Mewes HW, Ottenwalder B, Obermaier B, Tampe J, Heubner D, Wambutt R, Korn B, Klein M, Poustka A (Mar 2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166.
Kim, Young-Dae; Lee, Jung-Yoon; Oh, Kyu-Man; Araki, Masatake; Araki, Kimi; Yamamura, Ken-ichi; Jun, Chang-Duk (May 2011). "NSrp70 is a novel nuclear speckle-related protein that modulates alternative pre-mRNA splicing in vivo". Nucleic Acids Research. 39 (10): 4300–4314. doi:10.1093/nar/gkq1267. ISSN 1362-4962. PMC 3105421. PMID 21296756.
Chen, Yu; Belmont, Andrew S. (April 2019). "Genome organization around nuclear speckles". Current Opinion in Genetics & Development. 55: 91–99. doi:10.1016/j.gde.2019.06.008. ISSN 1879-0380. PMC 6759399. PMID 31394307.
Kim, Chang-Hyun; Kim, Young-Dae; Choi, Eun-Kyung; Kim, Hye-Ran; Na, Bo-Ra; Im, Sin-Hyeog; Jun, Chang-Duk (2016-03-18). "Nuclear Speckle-related Protein 70 Binds to Serine/Arginine-rich Splicing Factors 1 and 2 via an Arginine/Serine-like Region and Counteracts Their Alternative Splicing Activity". The Journal of Biological Chemistry. 291 (12): 6169–6181. doi:10.1074/jbc.M115.689414. ISSN 1083-351X. PMC 4813587. PMID 26797131.
Calame, Daniel G.; Bakhtiari, Somayeh; Logan, Rachel; Coban-Akdemir, Zeynep; Du, Haowei; Mitani, Tadahiro; Fatih, Jawid M.; Hunter, Jill V.; Herman, Isabella; Pehlivan, Davut; Jhangiani, Shalini N.; Person, Richard; Schnur, Rhonda E.; Jin, Sheng Chih; Bilguvar, Kaya (December 2021). "Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy". Genetics in Medicine. 23 (12): 2455–2460. doi:10.1038/s41436-021-01291-x. ISSN 1530-0366. PMC 8633036. PMID 34385670.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000126653 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000037958 – Ensembl, May 2017

nih.gov

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, Bocher M, Blocker H, Bauersachs S, Blum H, Lauber J, Dusterhoft A, Beyer A, Kohrer K, Strack N, Mewes HW, Ottenwalder B, Obermaier B, Tampe J, Heubner D, Wambutt R, Korn B, Klein M, Poustka A (Mar 2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166.
"NSRP1 nuclear speckle splicing regulatory protein 1 [ Homo sapiens (human) ]". 17 June 2024.
Kim, Young-Dae; Lee, Jung-Yoon; Oh, Kyu-Man; Araki, Masatake; Araki, Kimi; Yamamura, Ken-ichi; Jun, Chang-Duk (May 2011). "NSrp70 is a novel nuclear speckle-related protein that modulates alternative pre-mRNA splicing in vivo". Nucleic Acids Research. 39 (10): 4300–4314. doi:10.1093/nar/gkq1267. ISSN 1362-4962. PMC 3105421. PMID 21296756.
Chen, Yu; Belmont, Andrew S. (April 2019). "Genome organization around nuclear speckles". Current Opinion in Genetics & Development. 55: 91–99. doi:10.1016/j.gde.2019.06.008. ISSN 1879-0380. PMC 6759399. PMID 31394307.
Kim, Chang-Hyun; Kim, Young-Dae; Choi, Eun-Kyung; Kim, Hye-Ran; Na, Bo-Ra; Im, Sin-Hyeog; Jun, Chang-Duk (2016-03-18). "Nuclear Speckle-related Protein 70 Binds to Serine/Arginine-rich Splicing Factors 1 and 2 via an Arginine/Serine-like Region and Counteracts Their Alternative Splicing Activity". The Journal of Biological Chemistry. 291 (12): 6169–6181. doi:10.1074/jbc.M115.689414. ISSN 1083-351X. PMC 4813587. PMID 26797131.
Calame, Daniel G.; Bakhtiari, Somayeh; Logan, Rachel; Coban-Akdemir, Zeynep; Du, Haowei; Mitani, Tadahiro; Fatih, Jawid M.; Hunter, Jill V.; Herman, Isabella; Pehlivan, Davut; Jhangiani, Shalini N.; Person, Richard; Schnur, Rhonda E.; Jin, Sheng Chih; Bilguvar, Kaya (December 2021). "Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy". Genetics in Medicine. 23 (12): 2455–2460. doi:10.1038/s41436-021-01291-x. ISSN 1530-0366. PMC 8633036. PMID 34385670.

pubmed.ncbi.nlm.nih.gov

Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, Bocher M, Blocker H, Bauersachs S, Blum H, Lauber J, Dusterhoft A, Beyer A, Kohrer K, Strack N, Mewes HW, Ottenwalder B, Obermaier B, Tampe J, Heubner D, Wambutt R, Korn B, Klein M, Poustka A (Mar 2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166.
Kim, Young-Dae; Lee, Jung-Yoon; Oh, Kyu-Man; Araki, Masatake; Araki, Kimi; Yamamura, Ken-ichi; Jun, Chang-Duk (May 2011). "NSrp70 is a novel nuclear speckle-related protein that modulates alternative pre-mRNA splicing in vivo". Nucleic Acids Research. 39 (10): 4300–4314. doi:10.1093/nar/gkq1267. ISSN 1362-4962. PMC 3105421. PMID 21296756.
Chen, Yu; Belmont, Andrew S. (April 2019). "Genome organization around nuclear speckles". Current Opinion in Genetics & Development. 55: 91–99. doi:10.1016/j.gde.2019.06.008. ISSN 1879-0380. PMC 6759399. PMID 31394307.
Kim, Chang-Hyun; Kim, Young-Dae; Choi, Eun-Kyung; Kim, Hye-Ran; Na, Bo-Ra; Im, Sin-Hyeog; Jun, Chang-Duk (2016-03-18). "Nuclear Speckle-related Protein 70 Binds to Serine/Arginine-rich Splicing Factors 1 and 2 via an Arginine/Serine-like Region and Counteracts Their Alternative Splicing Activity". The Journal of Biological Chemistry. 291 (12): 6169–6181. doi:10.1074/jbc.M115.689414. ISSN 1083-351X. PMC 4813587. PMID 26797131.
Calame, Daniel G.; Bakhtiari, Somayeh; Logan, Rachel; Coban-Akdemir, Zeynep; Du, Haowei; Mitani, Tadahiro; Fatih, Jawid M.; Hunter, Jill V.; Herman, Isabella; Pehlivan, Davut; Jhangiani, Shalini N.; Person, Richard; Schnur, Rhonda E.; Jin, Sheng Chih; Bilguvar, Kaya (December 2021). "Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy". Genetics in Medicine. 23 (12): 2455–2460. doi:10.1038/s41436-021-01291-x. ISSN 1530-0366. PMC 8633036. PMID 34385670.

omim.org

"Entry - #620001 - NEURODEVELOPMENTAL DISORDER WITH SPASTICITY, SEIZURES, AND BRAIN ABNORMALITIES; NEDSSBA - OMIM". omim.org. Retrieved 2023-01-22.

worldcat.org

search.worldcat.org

Kim, Young-Dae; Lee, Jung-Yoon; Oh, Kyu-Man; Araki, Masatake; Araki, Kimi; Yamamura, Ken-ichi; Jun, Chang-Duk (May 2011). "NSrp70 is a novel nuclear speckle-related protein that modulates alternative pre-mRNA splicing in vivo". Nucleic Acids Research. 39 (10): 4300–4314. doi:10.1093/nar/gkq1267. ISSN 1362-4962. PMC 3105421. PMID 21296756.
Chen, Yu; Belmont, Andrew S. (April 2019). "Genome organization around nuclear speckles". Current Opinion in Genetics & Development. 55: 91–99. doi:10.1016/j.gde.2019.06.008. ISSN 1879-0380. PMC 6759399. PMID 31394307.
Kim, Chang-Hyun; Kim, Young-Dae; Choi, Eun-Kyung; Kim, Hye-Ran; Na, Bo-Ra; Im, Sin-Hyeog; Jun, Chang-Duk (2016-03-18). "Nuclear Speckle-related Protein 70 Binds to Serine/Arginine-rich Splicing Factors 1 and 2 via an Arginine/Serine-like Region and Counteracts Their Alternative Splicing Activity". The Journal of Biological Chemistry. 291 (12): 6169–6181. doi:10.1074/jbc.M115.689414. ISSN 1083-351X. PMC 4813587. PMID 26797131.
Calame, Daniel G.; Bakhtiari, Somayeh; Logan, Rachel; Coban-Akdemir, Zeynep; Du, Haowei; Mitani, Tadahiro; Fatih, Jawid M.; Hunter, Jill V.; Herman, Isabella; Pehlivan, Davut; Jhangiani, Shalini N.; Person, Richard; Schnur, Rhonda E.; Jin, Sheng Chih; Bilguvar, Kaya (December 2021). "Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy". Genetics in Medicine. 23 (12): 2455–2460. doi:10.1038/s41436-021-01291-x. ISSN 1530-0366. PMC 8633036. PMID 34385670.