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RAB7A (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "RAB7A" in French language version.

refsWebsite
Global rank French rank
20nih.gov
4th place
12th place
18doi.org
2nd place
3rd place
1ojrd.com
low place
low place
1medscape.com
719th place
1,716th place

doi.org (Global: 2nd place; French: 3rd place)

dx.doi.org

  • « Cloning and mapping of human Rab7 and Rab9 cDNA sequences and identification of a Rab9 pseudogene », Genomics, vol. 41, no 1,‎ , p. 131–4 (PMID 9126495, DOI 10.1006/geno.1997.4644)
  • « NotI linking/jumping clones of human chromosome 3: mapping of the TFRC, RAB7 and HAUSP genes to regions rearranged in leukemia and deleted in solid tumors », FEBS Letters, vol. 419, nos 2–3,‎ , p. 181–5 (PMID 9428630, DOI 10.1016/S0014-5793(97)01449-X)
  • « Hereditary sensory neuropathy type I », Orphanet Journal of Rare Diseases, vol. 3, no 7,‎ , p. 7 (PMID 18348718, PMCID 2311280, DOI 10.1186/1750-1172-3-7, lire en ligne)
  • « Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy », American Journal of Human Genetics, vol. 72, no 3,‎ , p. 722–727 (PMID 12545426, PMCID 1180247, DOI 10.1086/367847)
  • « Molecular cloning and expression analysis of the human Rab7 GTP-ase complementary deoxyribonucleic acid », Biochemical and Biophysical Research Communications, vol. 229, no 3,‎ , p. 887–890 (PMID 8954989, DOI 10.1006/bbrc.1996.1897)
  • « Cloning and mapping of human Rab7 and Rab9 cDNA sequences and identification of a Rab9 pseudogene », Genomics, vol. 41, no 1,‎ , p. 131–134 (PMID 9126495, DOI 10.1006/geno.1997.4644)
  • « Rab7 prevents growth factor-independent survival by inhibiting cell-autonomous nutrient transporter expression », Developmental Cell, vol. 5, no 4,‎ , p. 571–82 (PMID 14536059, DOI 10.1016/s1534-5807(03)00291-0)
  • « Rab-interacting lysosomal protein (RILP): the Rab7 effector required for transport to lysosomes », The EMBO Journal, vol. 20, no 4,‎ , p. 683–93 (PMID 11179213, PMCID 145419, DOI 10.1093/emboj/20.4.683)
  • « Human Vam6p promotes lysosome clustering and fusion in vivo », The Journal of Cell Biology, vol. 154, no 1,‎ , p. 109–22 (PMID 11448994, PMCID 2196876, DOI 10.1083/jcb.200102142)
  • « Crystallization and preliminary X-ray diffraction analysis of monoprenylated Rab7 GTPase in complex with Rab escort protein 1 », Journal of Structural Biology, vol. 141, no 1,‎ , p. 93–5 (PMID 12576024, DOI 10.1016/S1047-8477(02)00634-2)
  • « Moderate discrimination of REP-1 between Rab7 x GDP and Rab7 x GTP arises from a difference of an order of magnitude in dissociation rates », FEBS Letters, vol. 425, no 3,‎ , p. 460–4 (PMID 9563513, DOI 10.1016/S0014-5793(98)00290-7)
  • « Structural basis for recruitment of RILP by small GTPase Rab7 », The EMBO Journal, vol. 24, no 8,‎ , p. 1491–1501 (PMID 15933719, PMCID 1142575, DOI 10.1038/sj.emboj.7600643)
  • « A unique region of RILP distinguishes it from its related proteins in its regulation of lysosomal morphology and interaction with Rab7 and Rab34 », Molecular Biology of the Cell, vol. 15, no 2,‎ , p. 815–826 (PMID 14668488, PMCID 329395, DOI 10.1091/mbc.E03-06-0413)
  • « Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments », Cellular and Molecular Life Sciences, vol. 69, no 12,‎ , p. 2075–2089 (PMID 22261744, DOI 10.1007/s00018-011-0913-1)
  • « Regulation of retromer recruitment to endosomes by sequential action of Rab5 and Rab7 », The Journal of Cell Biology, vol. 183, no 3,‎ , p. 513–26 (PMID 18981234, PMCID 2575791, DOI 10.1083/jcb.200804048)
  • « RAB7 controls melanoma progression by exploiting a lineage-specific wiring of the endolysosomal pathway », Cancer Cell, vol. 26, no 1,‎ , p. 61–76 (PMID 24981740, DOI 10.1016/j.ccr.2014.04.030)
  • « Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A », Brain, vol. 123, no 7,‎ , p. 1516–27 (PMID 10869062, DOI 10.1093/brain/123.7.1516)
  • « Human Rab7 mutation mimics features of Charcot-Marie-Tooth neuropathy type 2B in Drosophila », Neurobiology of Disease, vol. 65,‎ , p. 211–9 (PMID 24521780, DOI 10.1016/j.nbd.2014.01.021)

medscape.com (Global: 719th place; French: 1,716th place)

emedicine.medscape.com

nih.gov (Global: 4th place; French: 12th place)

ncbi.nlm.nih.gov

  • « Cloning and mapping of human Rab7 and Rab9 cDNA sequences and identification of a Rab9 pseudogene », Genomics, vol. 41, no 1,‎ , p. 131–4 (PMID 9126495, DOI 10.1006/geno.1997.4644)
  • « NotI linking/jumping clones of human chromosome 3: mapping of the TFRC, RAB7 and HAUSP genes to regions rearranged in leukemia and deleted in solid tumors », FEBS Letters, vol. 419, nos 2–3,‎ , p. 181–5 (PMID 9428630, DOI 10.1016/S0014-5793(97)01449-X)
  • « Hereditary sensory neuropathy type I », Orphanet Journal of Rare Diseases, vol. 3, no 7,‎ , p. 7 (PMID 18348718, PMCID 2311280, DOI 10.1186/1750-1172-3-7, lire en ligne)
  • « Entrez Gene: RAB7A RAB7A, member RAS oncogene family »
  • « Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy », American Journal of Human Genetics, vol. 72, no 3,‎ , p. 722–727 (PMID 12545426, PMCID 1180247, DOI 10.1086/367847)
  • « Molecular cloning and expression analysis of the human Rab7 GTP-ase complementary deoxyribonucleic acid », Biochemical and Biophysical Research Communications, vol. 229, no 3,‎ , p. 887–890 (PMID 8954989, DOI 10.1006/bbrc.1996.1897)
  • « Cloning and mapping of human Rab7 and Rab9 cDNA sequences and identification of a Rab9 pseudogene », Genomics, vol. 41, no 1,‎ , p. 131–134 (PMID 9126495, DOI 10.1006/geno.1997.4644)
  • « Rab7 prevents growth factor-independent survival by inhibiting cell-autonomous nutrient transporter expression », Developmental Cell, vol. 5, no 4,‎ , p. 571–82 (PMID 14536059, DOI 10.1016/s1534-5807(03)00291-0)
  • « Rab-interacting lysosomal protein (RILP): the Rab7 effector required for transport to lysosomes », The EMBO Journal, vol. 20, no 4,‎ , p. 683–93 (PMID 11179213, PMCID 145419, DOI 10.1093/emboj/20.4.683)
  • « Human Vam6p promotes lysosome clustering and fusion in vivo », The Journal of Cell Biology, vol. 154, no 1,‎ , p. 109–22 (PMID 11448994, PMCID 2196876, DOI 10.1083/jcb.200102142)
  • « Crystallization and preliminary X-ray diffraction analysis of monoprenylated Rab7 GTPase in complex with Rab escort protein 1 », Journal of Structural Biology, vol. 141, no 1,‎ , p. 93–5 (PMID 12576024, DOI 10.1016/S1047-8477(02)00634-2)
  • « Moderate discrimination of REP-1 between Rab7 x GDP and Rab7 x GTP arises from a difference of an order of magnitude in dissociation rates », FEBS Letters, vol. 425, no 3,‎ , p. 460–4 (PMID 9563513, DOI 10.1016/S0014-5793(98)00290-7)
  • « Structural basis for recruitment of RILP by small GTPase Rab7 », The EMBO Journal, vol. 24, no 8,‎ , p. 1491–1501 (PMID 15933719, PMCID 1142575, DOI 10.1038/sj.emboj.7600643)
  • « A unique region of RILP distinguishes it from its related proteins in its regulation of lysosomal morphology and interaction with Rab7 and Rab34 », Molecular Biology of the Cell, vol. 15, no 2,‎ , p. 815–826 (PMID 14668488, PMCID 329395, DOI 10.1091/mbc.E03-06-0413)
  • « Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments », Cellular and Molecular Life Sciences, vol. 69, no 12,‎ , p. 2075–2089 (PMID 22261744, DOI 10.1007/s00018-011-0913-1)
  • « Regulation of retromer recruitment to endosomes by sequential action of Rab5 and Rab7 », The Journal of Cell Biology, vol. 183, no 3,‎ , p. 513–26 (PMID 18981234, PMCID 2575791, DOI 10.1083/jcb.200804048)
  • « RAB7 controls melanoma progression by exploiting a lineage-specific wiring of the endolysosomal pathway », Cancer Cell, vol. 26, no 1,‎ , p. 61–76 (PMID 24981740, DOI 10.1016/j.ccr.2014.04.030)
  • « Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A », Brain, vol. 123, no 7,‎ , p. 1516–27 (PMID 10869062, DOI 10.1093/brain/123.7.1516)
  • « Human Rab7 mutation mimics features of Charcot-Marie-Tooth neuropathy type 2B in Drosophila », Neurobiology of Disease, vol. 65,‎ , p. 211–9 (PMID 24521780, DOI 10.1016/j.nbd.2014.01.021)

ghr.nlm.nih.gov

ojrd.com (Global: low place; French: low place)