ABCA4 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ABCA4" in Chinese language version.

Last modified: 02:43:16, 24 July 2026 (UTC)

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1312doi.org

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65archive.org

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62ensembl.org

630^th place

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54semanticscholar.org

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11hdl.handle.net

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archive.org (Global: 6^th place; Chinese: 2^nd place)

Nasonkin I, Illing M, Koehler MR, Schmid M, Molday RS, Weber BH. Mapping of the rod photoreceptor ABC transporter (ABCR) to 1p21-p22.1 and identification of novel mutations in Stargardt's disease. Human Genetics. January 1998, 102 (1): 21–6. PMID 9490294. S2CID 22070963. doi:10.1007/s004390050649.
Sun H, Nathans J. ABCR: rod photoreceptor-specific ABC transporter responsible for Stargardt disease. Methods in Enzymology. 2000, 315: 879–97. ISBN 978-0-12-182216-3. PMID 10736747. doi:10.1016/S0076-6879(00)15888-4.
Weng J, Mata NL, Azarian SM, Tzekov RT, Birch DG, Travis GH. Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice. Cell. July 1999, 98 (1): 13–23. PMID 10412977. S2CID 18605680. doi:10.1016/S0092-8674(00)80602-9 .
Molday RS, Beharry S, Ahn J, Zhong M. Binding of N-retinylidene-PE to ABCA4 and a model for its transport across membranes. Advances in Experimental Medicine and Biology. 2006, 572: 465–70. ISBN 978-0-387-28464-4. PMID 17249610. doi:10.1007/0-387-32442-9_64.
Maeda A, Maeda T, Golczak M, Palczewski K. Retinopathy in mice induced by disrupted all-trans-retinal clearance. The Journal of Biological Chemistry. September 2008, 283 (39): 26684–93. PMC 2546559 . PMID 18658157. doi:10.1074/jbc.M804505200 .

doi.org (Global: 2^nd place; Chinese: 5^th place)

Allikmets R, Singh N, Sun H, Shroyer NF, Hutchinson A, Chidambaram A, Gerrard B, Baird L, Stauffer D, Peiffer A, Rattner A, Smallwood P, Li Y, Anderson KL, Lewis RA, Nathans J, Leppert M, Dean M, Lupski JR. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nature Genetics. March 1997, 15 (3): 236–46. PMID 9054934. S2CID 31677978. doi:10.1038/ng0397-236.
Nasonkin I, Illing M, Koehler MR, Schmid M, Molday RS, Weber BH. Mapping of the rod photoreceptor ABC transporter (ABCR) to 1p21-p22.1 and identification of novel mutations in Stargardt's disease. Human Genetics. January 1998, 102 (1): 21–6. PMID 9490294. S2CID 22070963. doi:10.1007/s004390050649.
Allikmets R, Shroyer NF, Singh N, Seddon JM, Lewis RA, Bernstein PS, Peiffer A, Zabriskie NA, Li Y, Hutchinson A, Dean M, Lupski JR, Leppert M. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Science. September 1997, 277 (5333): 1805–7 [2023-01-31]. PMID 9295268. doi:10.1126/science.277.5333.1805. （原始内容存档于2023-01-31）.
Sun H, Nathans J. ABCR: rod photoreceptor-specific ABC transporter responsible for Stargardt disease. Methods in Enzymology. 2000, 315: 879–97. ISBN 978-0-12-182216-3. PMID 10736747. doi:10.1016/S0076-6879(00)15888-4.
van Meer G, Halter D, Sprong H, Somerharju P, Egmond MR. ABC lipid transporters: extruders, flippases, or flopless activators?. FEBS Letters. February 2006, 580 (4): 1171–7. PMID 16376334. S2CID 27946190. doi:10.1016/j.febslet.2005.12.019. hdl:1874/19996 .
Sullivan JM. Focus on molecules: ABCA4 (ABCR)--an import-directed photoreceptor retinoid flipase. Experimental Eye Research. November 2009, 89 (5): 602–3. PMC 3371273 . PMID 19306869. doi:10.1016/j.exer.2009.03.005.
Weng J, Mata NL, Azarian SM, Tzekov RT, Birch DG, Travis GH. Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice. Cell. July 1999, 98 (1): 13–23. PMID 10412977. S2CID 18605680. doi:10.1016/S0092-8674(00)80602-9 .
Molday RS, Beharry S, Ahn J, Zhong M. Binding of N-retinylidene-PE to ABCA4 and a model for its transport across membranes. Advances in Experimental Medicine and Biology. 2006, 572: 465–70. ISBN 978-0-387-28464-4. PMID 17249610. doi:10.1007/0-387-32442-9_64.
Maeda A, Maeda T, Golczak M, Palczewski K. Retinopathy in mice induced by disrupted all-trans-retinal clearance. The Journal of Biological Chemistry. September 2008, 283 (39): 26684–93. PMC 2546559 . PMID 18658157. doi:10.1074/jbc.M804505200 .
Dixon MJ, Marazita ML, Beaty TH, Murray JC. Cleft lip and palate: understanding genetic and environmental influences. Nature Reviews Genetics. March 2011, 12 (3): 167–78. PMC 3086810 . PMID 21331089. doi:10.1038/nrg2933.
Beaty TH, Ruczinski I, Murray JC, Marazita ML, Munger RG, Hetmanski JB, Murray T, Redett RJ, Fallin MD, Liang KY, Wu T, Patel PJ, Jin SC, Zhang TX, Schwender H, Wu-Chou YH, Chen PK, Chong SS, Cheah F, Yeow V, Ye X, Wang H, Huang S, Jabs EW, Shi B, Wilcox AJ, Lie RT, Jee SH, Christensen K, Doheny KF, Pugh EW, Ling H, Scott AF. Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. Genetic Epidemiology. September 2011, 35 (6): 469–78. PMC 3180858 . PMID 21618603. doi:10.1002/gepi.20595.
Leslie EJ, Mansilla MA, Biggs LC, Schuette K, Bullard S, Cooper M, Dunnwald M, Lidral AC, Marazita ML, Beaty TH, Murray JC. Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22. Birth Defects Research. Part A, Clinical and Molecular Teratology. November 2012, 94 (11): 934–42. PMC 3501616 . PMID 23008150. doi:10.1002/bdra.23076.

ensembl.org (Global: 630^th place; Chinese: 669^th place)

may2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000198691 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000028125 – Ensembl, 2017年5月

expasy.org (Global: 5,863^rd place; Chinese: 1,125^th place)

web.expasy.org

视网膜特异性磷脂转运 ATPase ABCA4 (EC 7.6.2.1)｜Expasy - ProtParam. web.expasy.org (注：分子式计算是基于8个N连接的天冬酰胺ManₙGlcNAc₂位点：98，415，444，504，1469，1529，1588和6个二硫键得出n=n₁+n₂+n₃+n₄+n₅+n₆+n₇+n₈). [2026-07-24].

hdl.handle.net (Global: 66^th place; Chinese: 243^rd place)

van Meer G, Halter D, Sprong H, Somerharju P, Egmond MR. ABC lipid transporters: extruders, flippases, or flopless activators?. FEBS Letters. February 2006, 580 (4): 1171–7. PMID 16376334. S2CID 27946190. doi:10.1016/j.febslet.2005.12.019. hdl:1874/19996 .

nih.gov (Global: 5^th place; Chinese: 3^rd place)

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: ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4. [2023-01-31]. （原始内容存档于2023-01-31）.
Allikmets R, Singh N, Sun H, Shroyer NF, Hutchinson A, Chidambaram A, Gerrard B, Baird L, Stauffer D, Peiffer A, Rattner A, Smallwood P, Li Y, Anderson KL, Lewis RA, Nathans J, Leppert M, Dean M, Lupski JR. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nature Genetics. March 1997, 15 (3): 236–46. PMID 9054934. S2CID 31677978. doi:10.1038/ng0397-236.
Nasonkin I, Illing M, Koehler MR, Schmid M, Molday RS, Weber BH. Mapping of the rod photoreceptor ABC transporter (ABCR) to 1p21-p22.1 and identification of novel mutations in Stargardt's disease. Human Genetics. January 1998, 102 (1): 21–6. PMID 9490294. S2CID 22070963. doi:10.1007/s004390050649.
Allikmets R, Shroyer NF, Singh N, Seddon JM, Lewis RA, Bernstein PS, Peiffer A, Zabriskie NA, Li Y, Hutchinson A, Dean M, Lupski JR, Leppert M. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Science. September 1997, 277 (5333): 1805–7 [2023-01-31]. PMID 9295268. doi:10.1126/science.277.5333.1805. （原始内容存档于2023-01-31）.
Sun H, Nathans J. ABCR: rod photoreceptor-specific ABC transporter responsible for Stargardt disease. Methods in Enzymology. 2000, 315: 879–97. ISBN 978-0-12-182216-3. PMID 10736747. doi:10.1016/S0076-6879(00)15888-4.
van Meer G, Halter D, Sprong H, Somerharju P, Egmond MR. ABC lipid transporters: extruders, flippases, or flopless activators?. FEBS Letters. February 2006, 580 (4): 1171–7. PMID 16376334. S2CID 27946190. doi:10.1016/j.febslet.2005.12.019. hdl:1874/19996 .
Sullivan JM. Focus on molecules: ABCA4 (ABCR)--an import-directed photoreceptor retinoid flipase. Experimental Eye Research. November 2009, 89 (5): 602–3. PMC 3371273 . PMID 19306869. doi:10.1016/j.exer.2009.03.005.
Weng J, Mata NL, Azarian SM, Tzekov RT, Birch DG, Travis GH. Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice. Cell. July 1999, 98 (1): 13–23. PMID 10412977. S2CID 18605680. doi:10.1016/S0092-8674(00)80602-9 .
Molday RS, Beharry S, Ahn J, Zhong M. Binding of N-retinylidene-PE to ABCA4 and a model for its transport across membranes. Advances in Experimental Medicine and Biology. 2006, 572: 465–70. ISBN 978-0-387-28464-4. PMID 17249610. doi:10.1007/0-387-32442-9_64.
Maeda A, Maeda T, Golczak M, Palczewski K. Retinopathy in mice induced by disrupted all-trans-retinal clearance. The Journal of Biological Chemistry. September 2008, 283 (39): 26684–93. PMC 2546559 . PMID 18658157. doi:10.1074/jbc.M804505200 .
Dixon MJ, Marazita ML, Beaty TH, Murray JC. Cleft lip and palate: understanding genetic and environmental influences. Nature Reviews Genetics. March 2011, 12 (3): 167–78. PMC 3086810 . PMID 21331089. doi:10.1038/nrg2933.
Beaty TH, Ruczinski I, Murray JC, Marazita ML, Munger RG, Hetmanski JB, Murray T, Redett RJ, Fallin MD, Liang KY, Wu T, Patel PJ, Jin SC, Zhang TX, Schwender H, Wu-Chou YH, Chen PK, Chong SS, Cheah F, Yeow V, Ye X, Wang H, Huang S, Jabs EW, Shi B, Wilcox AJ, Lie RT, Jee SH, Christensen K, Doheny KF, Pugh EW, Ling H, Scott AF. Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. Genetic Epidemiology. September 2011, 35 (6): 469–78. PMC 3180858 . PMID 21618603. doi:10.1002/gepi.20595.
Leslie EJ, Mansilla MA, Biggs LC, Schuette K, Bullard S, Cooper M, Dunnwald M, Lidral AC, Marazita ML, Beaty TH, Murray JC. Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22. Birth Defects Research. Part A, Clinical and Molecular Teratology. November 2012, 94 (11): 934–42. PMC 3501616 . PMID 23008150. doi:10.1002/bdra.23076.

semanticscholar.org (Global: 15^th place; Chinese: 141^st place)

api.semanticscholar.org

Allikmets R, Singh N, Sun H, Shroyer NF, Hutchinson A, Chidambaram A, Gerrard B, Baird L, Stauffer D, Peiffer A, Rattner A, Smallwood P, Li Y, Anderson KL, Lewis RA, Nathans J, Leppert M, Dean M, Lupski JR. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nature Genetics. March 1997, 15 (3): 236–46. PMID 9054934. S2CID 31677978. doi:10.1038/ng0397-236.
Nasonkin I, Illing M, Koehler MR, Schmid M, Molday RS, Weber BH. Mapping of the rod photoreceptor ABC transporter (ABCR) to 1p21-p22.1 and identification of novel mutations in Stargardt's disease. Human Genetics. January 1998, 102 (1): 21–6. PMID 9490294. S2CID 22070963. doi:10.1007/s004390050649.
van Meer G, Halter D, Sprong H, Somerharju P, Egmond MR. ABC lipid transporters: extruders, flippases, or flopless activators?. FEBS Letters. February 2006, 580 (4): 1171–7. PMID 16376334. S2CID 27946190. doi:10.1016/j.febslet.2005.12.019. hdl:1874/19996 .
Weng J, Mata NL, Azarian SM, Tzekov RT, Birch DG, Travis GH. Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice. Cell. July 1999, 98 (1): 13–23. PMID 10412977. S2CID 18605680. doi:10.1016/S0092-8674(00)80602-9 .

web.archive.org (Global: 1^st place; Chinese: 1^st place)

Entrez Gene: ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4. [2023-01-31]. （原始内容存档于2023-01-31）.
Allikmets R, Shroyer NF, Singh N, Seddon JM, Lewis RA, Bernstein PS, Peiffer A, Zabriskie NA, Li Y, Hutchinson A, Dean M, Lupski JR, Leppert M. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Science. September 1997, 277 (5333): 1805–7 [2023-01-31]. PMID 9295268. doi:10.1126/science.277.5333.1805. （原始内容存档于2023-01-31）.

zenodo.org (Global: 737^th place; Chinese: 1,063^rd place)

Allikmets R, Shroyer NF, Singh N, Seddon JM, Lewis RA, Bernstein PS, Peiffer A, Zabriskie NA, Li Y, Hutchinson A, Dean M, Lupski JR, Leppert M. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Science. September 1997, 277 (5333): 1805–7 [2023-01-31]. PMID 9295268. doi:10.1126/science.277.5333.1805. （原始内容存档于2023-01-31）.

ABCA4 (Chinese Wikipedia)

archive.org (Global: 6th place; Chinese: 2nd place)

doi.org (Global: 2nd place; Chinese: 5th place)

ensembl.org (Global: 630th place; Chinese: 669th place)

may2017.archive.ensembl.org

expasy.org (Global: 5,863rd place; Chinese: 1,125th place)