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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.
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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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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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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Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability.
Rangel-Sosa MM, Figuera-Villanueva LE, González-Ramos IA, Pérez-Páramo YX, Martínez-Jacobo LA, Arnaud-López L, Nastasi-Catanese JA, Rivas-Estilla AM, Galán-Huerta KA, Rojas-Martínez A, Ortiz-López R, Córdova-Fletes C.
Rangel-Sosa MM, et al.
Clin Genet. 2018 Jun;93(6):1229-1233. doi: 10.1111/cge.13235. Epub 2018 Mar 9.
Clin Genet. 2018.
PMID: 29437235
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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.
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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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