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Year | Number of Results |
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2017 | 2 |
2018 | 1 |
2020 | 2 |
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Page 1
Sympathetic axonal sprouting induces changes in macrophage populations and protects against pancreatic cancer.
Nat Commun. 2022 Apr 13;13(1):1985. doi: 10.1038/s41467-022-29659-w.
Nat Commun. 2022.
PMID: 35418199
Free PMC article.
Immunotherapy and gene therapy as novel treatments for cancer.
Rangel-Sosa MM, Aguilar-Córdova E, Rojas-Martínez A.
Rangel-Sosa MM, et al.
Colomb Med (Cali). 2017 Sep 30;48(3):138-147. doi: 10.25100/cm.v48i3.2997.
Colomb Med (Cali). 2017.
PMID: 29213157
Free PMC article.
Review.
Item in Clipboard
VPS35 deficiency in the embryonic cortex leads to prenatal cell loss and abnormal development of axonal connectivity.
Roque M, Alves Rodrigues de Souza D, Rangel-Sosa MM, Altounian M, Hocine M, Deloulme JC, Barbier EL, Mann F, Chauvet S.
Roque M, et al. Among authors: rangel sosa mm.
Mol Cell Neurosci. 2022 May;120:103726. doi: 10.1016/j.mcn.2022.103726. Epub 2022 Mar 31.
Mol Cell Neurosci. 2022.
PMID: 35367368
Free article.
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Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis.
Córdova-Fletes C, Rangel-Sosa MM, Martínez-Jacobo LA, Becerra-Solano LE, Arellano-Valdés CA, Tlacuilo-Parra JA, Galán-Huerta KA, Rivas-Estilla AM, Hernandez-Orozco AA, García-Ortiz JE.
Córdova-Fletes C, et al. Among authors: rangel sosa mm.
Autoimmunity. 2020 Sep;53(6):344-352. doi: 10.1080/08916934.2020.1786068. Epub 2020 Jun 29.
Autoimmunity. 2020.
PMID: 32597225
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Genomic Characterization of a Rare, de Novo Unbalanced ins(3;1)(p25.3;q21.3q23.3) in a Female Child with Multiple Congenital Anomalies.
Ornelas-Arana ML, Pérez-Garcia G, Robles-Espinoza CD, Rangel-Sosa MM, Castaneda-Garcia C, Juárez-Vázquez CI, López-Pérez LG, Pérez-Ornelas C, Hernández-Zaragoza G, Lara-Aguilar RA, Córdova-Fletes C.
Ornelas-Arana ML, et al. Among authors: rangel sosa mm.
Cytogenet Genome Res. 2020;160(10):579-588. doi: 10.1159/000511234. Epub 2020 Nov 5.
Cytogenet Genome Res. 2020.
PMID: 33152732
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Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies.
Córdova-Fletes C, Becerra-Solano LE, Rangel-Sosa MM, Rivas-Estilla AM, Alberto Galán-Huerta K, Ortiz-López R, Rojas-Martínez A, Juárez-Vázquez CI, García-Ortiz JE.
Córdova-Fletes C, et al. Among authors: rangel sosa mm.
Eur J Med Genet. 2018 Mar;61(3):161-167. doi: 10.1016/j.ejmg.2017.11.011. Epub 2017 Nov 23.
Eur J Med Genet. 2018.
PMID: 29174089
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