175 related articles for article (PubMed ID: 37345651)
1. SPECC1L: a cytoskeletal protein that regulates embryonic tissue dynamics.
Saadi I; Goering JP; Hufft-Martinez BM; Tran PV
Biochem Soc Trans; 2023 Jun; 51(3):949-958. PubMed ID: 37345651
[TBL] [Abstract][Full Text] [Related]
2. In-frame deletion of SPECC1L microtubule association domain results in gain-of-function phenotypes affecting embryonic tissue movement and fusion events.
Goering JP; Wenger LW; Stetsiv M; Moedritzer M; Hall EG; Isai DG; Jack BM; Umar Z; Rickabaugh MK; Czirok A; Saadi I
Hum Mol Genet; 2021 Dec; 31(1):18-31. PubMed ID: 34302166
[TBL] [Abstract][Full Text] [Related]
3. SPECC1L regulates palate development downstream of IRF6.
Hall EG; Wenger LW; Wilson NR; Undurty-Akella SS; Standley J; Augustine-Akpan EA; Kousa YA; Acevedo DS; Goering JP; Pitstick L; Natsume N; Paroya SM; Busch TD; Ito M; Mori A; Imura H; Schultz-Rogers LE; Klee EW; Babovic-Vuksanovic D; Kroc SA; Adeyemo WL; Eshete MA; Bjork BC; Suzuki S; Murray JC; Schutte BC; Butali A; Saadi I
Hum Mol Genet; 2020 Mar; 29(5):845-858. PubMed ID: 31943082
[TBL] [Abstract][Full Text] [Related]
4. Phenotypic spectrum associated with SPECC1L pathogenic variants: new families and critical review of the nosology of Teebi, Opitz GBBB, and Baraitser-Winter syndromes.
Bhoj EJ; Haye D; Toutain A; Bonneau D; Nielsen IK; Lund IB; Bogaard P; Leenskjold S; Karaer K; Wild KT; Grand KL; Astiazaran MC; Gonzalez-Nieto LA; Carvalho A; Lehalle D; Amudhavalli SM; Repnikova E; Saunders C; Thiffault I; Saadi I; Li D; Hakonarson H; Vial Y; Zackai E; Callier P; Drunat S; Verloes A
Eur J Med Genet; 2019 Dec; 62(12):103588. PubMed ID: 30472488
[TBL] [Abstract][Full Text] [Related]
5. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting.
Saadi I; Alkuraya FS; Gisselbrecht SS; Goessling W; Cavallesco R; Turbe-Doan A; Petrin AL; Harris J; Siddiqui U; Grix AW; Hove HD; Leboulch P; Glover TW; Morton CC; Richieri-Costa A; Murray JC; Erickson RP; Maas RL
Am J Hum Genet; 2011 Jul; 89(1):44-55. PubMed ID: 21703590
[TBL] [Abstract][Full Text] [Related]
6. SPECC1L deficiency results in increased adherens junction stability and reduced cranial neural crest cell delamination.
Wilson NR; Olm-Shipman AJ; Acevedo DS; Palaniyandi K; Hall EG; Kosa E; Stumpff KM; Smith GJ; Pitstick L; Liao EC; Bjork BC; Czirok A; Saadi I
Sci Rep; 2016 Jan; 6():17735. PubMed ID: 26787558
[TBL] [Abstract][Full Text] [Related]
7. Congenital diaphragmatic hernia as a prominent feature of a SPECC1L-related syndrome.
Wild KT; Gordon T; Bhoj EJ; Du H; Jhangiani SN; Posey JE; Lupski JR; Scott DA; Zackai EH
Am J Med Genet A; 2020 Dec; 182(12):2919-2925. PubMed ID: 32954677
[TBL] [Abstract][Full Text] [Related]
8. Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome.
Kruszka P; Li D; Harr MH; Wilson NR; Swarr D; McCormick EM; Chiavacci RM; Li M; Martinez AF; Hart RA; McDonald-McGinn DM; Deardorff MA; Falk MJ; Allanson JE; Hudson C; Johnson JP; Saadi I; Hakonarson H; Muenke M; Zackai EH
J Med Genet; 2015 Feb; 52(2):104-10. PubMed ID: 25412741
[TBL] [Abstract][Full Text] [Related]
9. A point mutation in Myh10 causes major defects in heart development and body wall closure.
Ma X; Adelstein RS
Circ Cardiovasc Genet; 2014 Jun; 7(3):257-65. PubMed ID: 24825879
[TBL] [Abstract][Full Text] [Related]
10. The spectraplakin Short stop is an actin-microtubule cross-linker that contributes to organization of the microtubule network.
Applewhite DA; Grode KD; Keller D; Zadeh AD; Slep KC; Rogers SL
Mol Biol Cell; 2010 May; 21(10):1714-24. PubMed ID: 20335501
[TBL] [Abstract][Full Text] [Related]
11. Morphogenesis of the mouse neural plate depends on distinct roles of cofilin 1 in apical and basal epithelial domains.
Grego-Bessa J; Hildebrand J; Anderson KV
Development; 2015 Apr; 142(7):1305-14. PubMed ID: 25742799
[TBL] [Abstract][Full Text] [Related]
12. Expanding the SPECC1L mutation phenotypic spectrum to include Teebi hypertelorism syndrome.
Bhoj EJ; Li D; Harr MH; Tian L; Wang T; Zhao Y; Qiu H; Kim C; Hoffman JD; Hakonarson H; Zackai EH
Am J Med Genet A; 2015 Nov; 167A(11):2497-502. PubMed ID: 26111080
[TBL] [Abstract][Full Text] [Related]
13. Nonmuscle myosin-2 isoforms.
Sellers JR; Heissler SM
Curr Biol; 2019 Apr; 29(8):R275-R278. PubMed ID: 31014482
[TBL] [Abstract][Full Text] [Related]
14. Formation and contraction of multicellular actomyosin cables facilitate lens placode invagination.
Houssin NS; Martin JB; Coppola V; Yoon SO; Plageman TF
Dev Biol; 2020 Jun; 462(1):36-49. PubMed ID: 32113830
[TBL] [Abstract][Full Text] [Related]
15. Myosin-II activity generates a dynamic steady state with continuous actin turnover in a minimal actin cortex.
Sonal ; Ganzinger KA; Vogel SK; Mücksch J; Blumhardt P; Schwille P
J Cell Sci; 2018 Dec; 132(4):. PubMed ID: 30538127
[TBL] [Abstract][Full Text] [Related]
16. SPECC1L binds the myosin phosphatase complex MYPT1/PP1β and can regulate its distribution between microtubules and filamentous actin.
Mehta V; Decan N; Ooi S; Gaudreau-Lapierre A; Copeland JW; Trinkle-Mulcahy L
J Biol Chem; 2023 Feb; 299(2):102893. PubMed ID: 36634848
[TBL] [Abstract][Full Text] [Related]
17. Rho-kinase-dependent actin turnover and actomyosin disassembly are necessary for mouse spinal neural tube closure.
Escuin S; Vernay B; Savery D; Gurniak CB; Witke W; Greene ND; Copp AJ
J Cell Sci; 2015 Jul; 128(14):2468-81. PubMed ID: 26040287
[TBL] [Abstract][Full Text] [Related]
18. Mutations in non-muscle myosin 2A disrupt the actomyosin cytoskeleton in Sertoli cells and cause male infertility.
Sung DC; Ahmad M; Lerma Cervantes CB; Zhang Y; Adelstein RS; Ma X
Dev Biol; 2021 Feb; 470():49-61. PubMed ID: 33188738
[TBL] [Abstract][Full Text] [Related]
19. Impaired cytoskeletal arrangements and failure of ventral body wall closure in chick embryos treated with rock inhibitor (Y-27632).
Duess JW; Puri P; Thompson J
Pediatr Surg Int; 2016 Jan; 32(1):45-58. PubMed ID: 26563157
[TBL] [Abstract][Full Text] [Related]
20. A novel SPECC1L mutation causing Teebi hypertelorism syndrome: Expanding phenotypic and genetic spectrum.
Zhang T; Wu Q; Zhu L; Wu D; Yang R; Qi M; Huang X
Eur J Med Genet; 2020 Apr; 63(4):103851. PubMed ID: 31953237
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
