Detalhe da pesquisa
1.
ATF4-dependent increase in mitochondrial-endoplasmic reticulum tethering following OPA1 deletion in skeletal muscle.
J Cell Physiol
; 239(4): e31204, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38419397
2.
Abnormal chondrocyte development in a zebrafish model of cblC syndrome restored by an MMACHC cobalamin binding mutant.
Differentiation
; 131: 74-81, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37167860
3.
Knockdown of hspg2 is associated with abnormal mandibular joint formation and neural crest cell dysfunction in zebrafish.
BMC Dev Biol
; 21(1): 7, 2021 03 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33678174
4.
Activation of WNT signaling restores the facial deficits in a zebrafish with defects in cholesterol metabolism.
Genesis
; 58(12): e23397, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33197123
5.
Hcfc1a regulates neural precursor proliferation and asxl1 expression in the developing brain.
BMC Neurosci
; 21(1): 27, 2020 06 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32522152
6.
Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities.
Hum Mol Genet
; 26(15): 2838-2849, 2017 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28449119
7.
Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development.
Hum Mol Genet
; 24(15): 4443-53, 2015 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25972376
8.
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1.
Am J Hum Genet
; 93(3): 506-14, 2013 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24011988
9.
Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression.
Dev Biol
; 396(1): 94-106, 2014 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25281006
10.
Overexpression of MMACHC Prevents Craniofacial Phenotypes Caused by Knockdown of znf143b.
Am J Undergrad Res
; 20(1): 77-84, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38617190
11.
Missense and nonsense mutations of the zebrafish hcfc1a gene result in contrasting mTor and radial glial phenotypes.
Gene
; 864: 147290, 2023 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36804358
12.
Abnormal chondrocyte intercalation in a zebrafish model of cblC syndrome restored by an MMACHC cobalamin binding mutant.
bioRxiv
; 2023 Jan 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36711998
13.
Characterization of the zebrafish gabra1sa43718/sa43718 germline loss of function allele confirms a function for Gabra1 in motility and nervous system development.
bioRxiv
; 2023 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36747751
14.
3D reconstruction of murine mitochondria reveals changes in structure during aging linked to the MICOS complex.
Aging Cell
; 22(12): e14009, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37960952
15.
Identification and regulation of c-Myb target genes in MCF-7 cells.
BMC Cancer
; 11: 30, 2011 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-21261996
16.
Leading by example: developing mentoring strategies to promote diversity and student success.
Mol Biol Cell
; 32(22): vo1, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34735267
17.
The role of HCFC1 in syndromic and non-syndromic intellectual disability.
Med Res Arch
; 8(6)2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-34164576
18.
Abnormal expression of GABAA receptor subunits and hypomotility upon loss of gabra1 in zebrafish.
Biol Open
; 9(4)2020 04 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32205311
19.
Mutations in the zebrafish hmgcs1 gene reveal a novel function for isoprenoids during red blood cell development.
Blood Adv
; 3(8): 1244-1254, 2019 04 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-30987969
20.
A focus on polarity: Investigating the role of orientation cues in mediating student performance on mRNA synthesis tasks in an introductory cell and molecular biology course.
Biochem Mol Biol Educ
; 45(6): 501-508, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28520272