Detalhe da pesquisa
1.
Highly reusable Bi2O3/electron-Cu-shuttle in-situ immobilized polyacrylonitrile fibrous mat for efficient photocatalytic degradation of methylene blue and rhodamine B dyes.
J Environ Manage
; 354: 120346, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38387350
2.
Retention of methyl iodide on metal and TEDA impregnated activated carbon using indigenously developed setup.
Environ Res
; 238(Pt 1): 117133, 2023 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37729960
3.
BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron disease.
Genet Med
; 24(12): 2487-2500, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36136088
4.
Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss.
Proc Natl Acad Sci U S A
; 116(4): 1347-1352, 2019 01 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-30610177
5.
Assessment of arsenic exposure by drinking well water and associated carcinogenic risk in peri-urban areas of Vehari, Pakistan.
Environ Geochem Health
; 42(1): 121-133, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31054072
6.
Cadmium Partitioning, Physiological and Oxidative Stress Responses in Marigold (Calendula calypso) Grown on Contaminated Soil: Implications for Phytoremediation.
Bull Environ Contam Toxicol
; 105(2): 270-276, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32661664
7.
Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss.
Clin Genet
; 96(6): 575-578, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31432506
8.
SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency.
Brain
; 141(3): 662-672, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29351582
9.
ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice.
Proc Natl Acad Sci U S A
; 113(21): 5993-8, 2016 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-27162350
10.
Effect of salinity on cadmium tolerance, ionic homeostasis and oxidative stress responses in conocarpus exposed to cadmium stress: Implications for phytoremediation.
Ecotoxicol Environ Saf
; 171: 146-153, 2019 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-30599432
11.
Study of land cover/land use changes using RS and GIS: a case study of Multan district, Pakistan.
Environ Monit Assess
; 192(1): 2, 2019 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31792634
12.
A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation.
Hum Mol Genet
; 24(9): 2482-91, 2015 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25601850
13.
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing.
Proc Natl Acad Sci U S A
; 111(27): 9864-8, 2014 Jul 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-24958875
14.
Helix 8 and the i3 loop of the muscarinic M3 receptor are crucial sites for its regulation by the Gß5-RGS7 complex.
Biochemistry
; 54(4): 1077-88, 2015 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25551629
15.
Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53.
Mol Genet Genomics
; 290(4): 1327-34, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25633957
16.
Allostery mediates ligand binding to WWOX tumor suppressor via a conformational switch.
J Mol Recognit
; 28(4): 220-31, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25703206
17.
Effect of osmolytes on the binding of EGR1 transcription factor to DNA.
Biopolymers
; 103(2): 74-87, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25269753
18.
PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum.
Brain
; 137(Pt 1): 69-77, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24355708
19.
Structures of YAP protein domains reveal promising targets for development of new cancer drugs.
Semin Cell Dev Biol
; 23(7): 827-33, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22609812
20.
De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis.
Hum Genet
; 133(6): 737-42, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24337657