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Search life-sciences literature (45,103,589 articles, preprints and more)

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Revealing the mechanisms of RAC3 in tumor aggressiveness, the immunotherapy response, and drug resistance in bladder cancer.
Gao H, Qiu Y, Zheng X, Xu T, Liu G
Front Oncol, 14:1466319, 16 Sep 2024
Cited by: 0 articles | PMID: 39351351 | PMCID: PMC11441374
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Molecular mechanisms driving the interactions between platelet and gastric cancer cells during peritoneal dissemination.
Nakayama T, Saito R, Furuya S, Higuchi Y, Matsuoka K, Takahashi K, Maruyama S, Shoda K, Takiguchi K, Shiraishi K, Kawaguchi Y, Amemiya H, Kawaida H, Tsukiji N, Shirai T, Suzuki-Inoue K, Ichikawa D
Oncol Lett, 28(4):498, 13 Aug 2024
Cited by: 0 articles | PMID: 39211304 | PMCID: PMC11358723
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Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiency.
Benavides-Nieto M, Adam F, Martin E, Boussard C, Lagresle-Peyrou C, Callebaut I, Kauskot A, Repérant C, Feng M, Bordet JC, Castelle M, Morelle G, Brouzes C, Zarhrate M, Panikulam P, Lambert N, Picard C, Bodet D, Rouger-Gaudichon J, [...] Moshous D
J Clin Invest, 134(17):e169994, 11 Jul 2024
Cited by: 0 articles | PMID: 39225097 | PMCID: PMC11364392
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Clinical and functional spectrum of RAC2-related immunodeficiency.
Donkó Á, Sharapova SO, Kabat J, Ganesan S, Hauck FH, Bergerson JRE, Marois L, Abbott J, Moshous D, Williams KW, Campbell N, Martin PL, Lagresle-Peyrou C, Trojan T, Kuzmenko NB, Deordieva EA, Raykina EV, Abers MS, Abolhassani H, [...] Hsu AP
Blood, 143(15):1476-1487, 01 Apr 2024
Cited by: 4 articles | PMID: 38194689
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De novo variants in DENND5B cause a neurodevelopmental disorder.
Scala M, Tomati V, Ferla M, Lena M, Cohen JS, Fatemi A, Brokamp E, Bican A, Phillips JA, Koziura ME, Nicouleau M, Rio M, Siquier K, Boddaert N, Musante I, Tamburro S, Baldassari S, Iacomino M, Scudieri P, [...] Zara F
Am J Hum Genet, 111(3):529-543, 21 Feb 2024
Cited by: 0 articles | PMID: 38387458 | PMCID: PMC10940048
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MRI Data Analysis in Malformations of Cortical Development.
Severino M, Tortora D, Scala M
Methods Mol Biol, 2794:281-292, 01 Jan 2024
Cited by: 0 articles | PMID: 38630237
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The "microcephalic hydrocephalus" paradox as a paradigm of altered neural stem cell biology.
Duy PQ, Mehta NH, Kahle KT
Cereb Cortex, 34(1):bhad432, 01 Jan 2024
Cited by: 1 article | PMID: 37991277
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DAG1 haploinsufficiency is associated with sporadic and familial isolated or pauci-symptomatic hyperCKemia.
Traverso M, Baratto S, Iacomino M, Di Duca M, Panicucci C, Casalini S, Grandis M, Falace A, Torella A, Picillo E, Onore ME, Politano L, Nigro V, Innes AM, Barresi R, Bruno C, Zara F, Fiorillo C, Scala M
Eur J Hum Genet, 32(3):342-349, 04 Jan 2024
Cited by: 1 article | PMID: 38177406
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An unusual presentation of de novo RAC3 variation in prenatal diagnosis.
Meunier C, Cassart M, Kostyla K, Simonis N, Monestier O, Tessier A
Childs Nerv Syst, 40(5):1597-1602, 12 Jan 2024
Cited by: 0 articles | PMID: 38214746 | PMCID: PMC11026260
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Case Report: Novel biallelic moderately damaging variants in RTTN in a patient with cerebellar dysplasia.
Romano F, Amadori E, Madia F, Severino M, Capra V, Rizzo R, Barone R, Corradi B, Maragliano L, Shams Nosrati MS, Falace A, Striano P, Zara F, Scala M
Front Pediatr, 11:1326552, 21 Dec 2023
Cited by: 0 articles | PMID: 38178912 | PMCID: PMC10764497
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Live Imaging of Migrating Neurons and Glial Progenitors Visualized by in Utero Electroporation.
Nishikawa M, Nagata KI, Tabata H
Methods Mol Biol, 2794:201-209, 01 Jan 2024
Cited by: 0 articles | PMID: 38630231
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DDX3X Syndrome Behavioral Manifestations with Particular Emphasis on Psycho-Pathological Symptoms-A Review.
Stefaniak U, Malak R, Kaczmarek A, Samborski W, Mojs E
Biomedicines, 11(11):3046, 14 Nov 2023
Cited by: 0 articles | PMID: 38002045
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A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association.
Seyama R, Nishikawa M, Uchiyama Y, Hamada K, Yamamoto Y, Takeda M, Ochi T, Kishi M, Suzuki T, Hamanaka K, Fujita A, Tsuchida N, Koshimizu E, Misawa K, Miyatake S, Mizuguchi T, Makino S, Yao T, Ito H, [...] Matsumoto N
Sci Rep, 13(1):9789, 16 Jun 2023
Cited by: 0 articles | PMID: 37328543 | PMCID: PMC10275923
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The Evaluation of Rac1 Signaling as a Potential Therapeutic Target of Alzheimer's Disease.
Wang H, Yamahashi Y, Riedl M, Amano M, Kaibuchi K
Int J Mol Sci, 24(15):11880, 25 Jul 2023
Cited by: 1 article | PMID: 37569255 | PMCID: PMC10418761
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Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants.
Priolo M, Zara E, Radio FC, Ciolfi A, Spadaro F, Bellacchio E, Mancini C, Pantaleoni F, Cordeddu V, Chiriatti L, Niceta M, Africa E, Mammì C, Melis D, Coppola S, Tartaglia M
Eur J Hum Genet, 31(7):805-814, 14 Apr 2023
Cited by: 2 articles | PMID: 37059841
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Expression Analyses of Rich2/Arhgap44, a Rho Family GTPase-Activating Protein, during Mouse Brain Development.
Goto N, Nishikawa M, Ito H, Noda M, Hamada N, Tabata H, Kinoshita M, Nagata KI
Dev Neurosci, 45(1):19-26, 11 Jan 2023
Cited by: 2 articles | PMID: 36630934 | PMCID: PMC10129027
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The molecular basis of p21-activated kinase-associated neurodevelopmental disorders: From genotype to phenotype.
Dobrigna M, Poëa-Guyon S, Rousseau V, Vincent A, Toutain A, Barnier JV
Front Neurosci, 17:1123784, 02 Mar 2023
Cited by: 2 articles | PMID: 36937657 | PMCID: PMC10017488
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1-17 of 17 results

Search life-sciences literature (45,103,589 articles, preprints and more)

Search results

Revealing the mechanisms of RAC3 in tumor aggressiveness, the immunotherapy response, and drug resistance in bladder cancer.

Molecular mechanisms driving the interactions between platelet and gastric cancer cells during peritoneal dissemination.

Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiency.

Clinical and functional spectrum of RAC2-related immunodeficiency.

De novo variants in DENND5B cause a neurodevelopmental disorder.

MRI Data Analysis in Malformations of Cortical Development.

The "microcephalic hydrocephalus" paradox as a paradigm of altered neural stem cell biology.

DAG1 haploinsufficiency is associated with sporadic and familial isolated or pauci-symptomatic hyperCKemia.

An unusual presentation of de novo RAC3 variation in prenatal diagnosis.

Case Report: Novel biallelic moderately damaging variants in RTTN in a patient with cerebellar dysplasia.

Live Imaging of Migrating Neurons and Glial Progenitors Visualized by in Utero Electroporation.

DDX3X Syndrome Behavioral Manifestations with Particular Emphasis on Psycho-Pathological Symptoms-A Review.

A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association.

The Evaluation of Rac1 Signaling as a Potential Therapeutic Target of Alzheimer's Disease.

Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants.

Expression Analyses of Rich2/Arhgap44, a Rho Family GTPase-Activating Protein, during Mouse Brain Development.

The molecular basis of p21-activated kinase-associated neurodevelopmental disorders: From genotype to phenotype.

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