CRX (gene) (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "CRX (gene)" in English language version.

refsWebsite

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12nih.gov

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6doi.org

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2ensembl.org

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2semanticscholar.org

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1handle.net

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doi.org

Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, et al. (Nov 1997). "Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor". Cell. 91 (4): 543–53. doi:10.1016/S0092-8674(00)80440-7. hdl:10261/270606. PMID 9390563. S2CID 5755412.
Freund CL, Wang QL, Chen S, Muskat BL, Wiles CD, Sheffield VC, et al. (Apr 1998). "De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis". Nature Genetics. 18 (4): 311–2. doi:10.1038/ng0498-311. PMID 9537410. S2CID 22131800.
Tran NM, Zhang A, Zhang X, Huecker JB, Hennig AK, Chen S (Feb 6, 2014). "Mechanistically Distinct Mouse Models for CRX-Associated Retinopathy". PLOS Genet. 10 (2): e1004111. doi:10.1371/journal.pgen.1004111. PMC 3916252. PMID 24516401.
Clanor PB, Buchholz CN, Hayes JE, Friedman MA, White AM, Enke RA, et al. (March 23, 2022). "Structural and functional analysis of the human cone-rod homeobox transcription factor". Proteins. 90 (8): 1584–1593. doi:10.1002/prot.26332. PMC 9271546. PMID 35255174.
Germot A, Lecointre G, Plouhinec JL, Le Mentec C, Girardot F, Mazan S (September 2001). "Structural evolution of Otx genes in craniates". Molecular Biology and Evolution. 18 (9): 1668–78. doi:10.1093/oxfordjournals.molbev.a003955. PMID 11504847.
Maeso I, Dunwell TL, Wyatt CD, Marlétaz F, Vető B, Bernal JA, et al. (June 2016). "Evolutionary origin and functional divergence of totipotent cell homeobox genes in eutherian mammals". BMC Biology. 14 (1): 45. doi:10.1186/s12915-016-0267-0. PMC 4904359. PMID 27296695.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000105392 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000041578 – Ensembl, May 2017

handle.net

hdl.handle.net

Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, et al. (Nov 1997). "Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor". Cell. 91 (4): 543–53. doi:10.1016/S0092-8674(00)80440-7. hdl:10261/270606. PMID 9390563. S2CID 5755412.

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.
"Entrez Gene: CRX cone-rod homeobox".
Tran NM, Zhang A, Zhang X, Huecker JB, Hennig AK, Chen S (Feb 6, 2014). "Mechanistically Distinct Mouse Models for CRX-Associated Retinopathy". PLOS Genet. 10 (2): e1004111. doi:10.1371/journal.pgen.1004111. PMC 3916252. PMID 24516401.
Clanor PB, Buchholz CN, Hayes JE, Friedman MA, White AM, Enke RA, et al. (March 23, 2022). "Structural and functional analysis of the human cone-rod homeobox transcription factor". Proteins. 90 (8): 1584–1593. doi:10.1002/prot.26332. PMC 9271546. PMID 35255174.
Maeso I, Dunwell TL, Wyatt CD, Marlétaz F, Vető B, Bernal JA, et al. (June 2016). "Evolutionary origin and functional divergence of totipotent cell homeobox genes in eutherian mammals". BMC Biology. 14 (1): 45. doi:10.1186/s12915-016-0267-0. PMC 4904359. PMID 27296695.

pubmed.ncbi.nlm.nih.gov

Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, et al. (Nov 1997). "Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor". Cell. 91 (4): 543–53. doi:10.1016/S0092-8674(00)80440-7. hdl:10261/270606. PMID 9390563. S2CID 5755412.
Freund CL, Wang QL, Chen S, Muskat BL, Wiles CD, Sheffield VC, et al. (Apr 1998). "De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis". Nature Genetics. 18 (4): 311–2. doi:10.1038/ng0498-311. PMID 9537410. S2CID 22131800.
Tran NM, Zhang A, Zhang X, Huecker JB, Hennig AK, Chen S (Feb 6, 2014). "Mechanistically Distinct Mouse Models for CRX-Associated Retinopathy". PLOS Genet. 10 (2): e1004111. doi:10.1371/journal.pgen.1004111. PMC 3916252. PMID 24516401.
Clanor PB, Buchholz CN, Hayes JE, Friedman MA, White AM, Enke RA, et al. (March 23, 2022). "Structural and functional analysis of the human cone-rod homeobox transcription factor". Proteins. 90 (8): 1584–1593. doi:10.1002/prot.26332. PMC 9271546. PMID 35255174.
Germot A, Lecointre G, Plouhinec JL, Le Mentec C, Girardot F, Mazan S (September 2001). "Structural evolution of Otx genes in craniates". Molecular Biology and Evolution. 18 (9): 1668–78. doi:10.1093/oxfordjournals.molbev.a003955. PMID 11504847.
Maeso I, Dunwell TL, Wyatt CD, Marlétaz F, Vető B, Bernal JA, et al. (June 2016). "Evolutionary origin and functional divergence of totipotent cell homeobox genes in eutherian mammals". BMC Biology. 14 (1): 45. doi:10.1186/s12915-016-0267-0. PMC 4904359. PMID 27296695.

semanticscholar.org

api.semanticscholar.org

Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, et al. (Nov 1997). "Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor". Cell. 91 (4): 543–53. doi:10.1016/S0092-8674(00)80440-7. hdl:10261/270606. PMID 9390563. S2CID 5755412.
Freund CL, Wang QL, Chen S, Muskat BL, Wiles CD, Sheffield VC, et al. (Apr 1998). "De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis". Nature Genetics. 18 (4): 311–2. doi:10.1038/ng0498-311. PMID 9537410. S2CID 22131800.