受强制性开放获取政策约束的文章 - Abdul Nasir了解详情
无法在其他位置公开访问的文章:2 篇
Mitochondria-targeting nanozyme alleviating temporomandibular joint pain by inhibiting the TNFα/NF-κB/NEAT1 pathway
Q Bai, Y Zhou, X Cui, H Si, T Wu, A Nasir, H Ma, J Xing, Y Wang, X Cheng, ...
Journal of Materials Chemistry B 12 (1), 112-121, 2024
强制性开放获取政策: 国家自然科学基金委员会
TET1-mediated epigenetic regulation of tumor necrosis factor-α in trigeminal ganglia contributes to chronic temporomandibular joint pain
Z Wang, H Ma, A Nasir, S Liu, Z Li, F Tao, Q Bai
Life Sciences 336, 122283, 2024
强制性开放获取政策: 国家自然科学基金委员会
可在其他位置公开访问的文章:23 篇
Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance
K Liaqat, I Schrauwen, SI Raza, K Lee, S Hussain, I Chakchouk, A Nasir, ...
Journal of human genetics 64 (2), 153-160, 2019
强制性开放获取政策: US National Institutes of Health
Autosomal dominantly inherited GREB1L variants in individuals with profound sensorineural hearing impairment
I Schrauwen, K Liaqat, I Schatteman, T Bharadwaj, A Nasir, A Acharya, ...
Genes 11 (6), 687, 2020
强制性开放获取政策: US National Institutes of Health
Mechanism of zinc ejection by disulfiram in nonstructural protein 5A
AU Rehman, G Zhen, B Zhong, D Ni, J Li, A Nasir, MT Gabr, H Rafiq, ...
Physical Chemistry Chemical Physics 23 (21), 12204-12215, 2021
强制性开放获取政策: 国家自然科学基金委员会
A novel missense variant in the PNPLA1 gene underlies congenital ichthyosis in three consanguineous families
F Ahmad, M Ansar, S Mehmood, A Izoduwa, K Lee, A Nasir, M Abrar, ...
Journal of the European Academy of Dermatology and Venereology: JEADV 30 (12 …, 2015
强制性开放获取政策: US National Institutes of Health
Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis
I Schrauwen, H Valgaeren, L Tomas-Roca, M Sommen, U Altunoglu, ...
Genetics in Medicine 21 (5), 1199-1208, 2019
强制性开放获取政策: Research Foundation (Flanders), Government of Spain, Belgian Science Policy …
A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment
I Schrauwen, I Chakchouk, K Liaqat, A Jan, A Nasir, S Hussain, ...
Human genetics 137, 471-478, 2018
强制性开放获取政策: US National Institutes of Health
Tyrosinase (TYR) gene sequencing and literature review reveals recurrent mutations and multiple population founder gene mutations as causative of …
M Shakil, GV Harlalka, S Ali, S Lin, I D’Atri, S Hussain, A Nasir, ...
Eye 33 (8), 1339-1346, 2019
强制性开放获取政策: Wellcome Trust
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes
A Wonkam, SM Adadey, I Schrauwen, ET Aboagye, E Wonkam-Tingang, ...
Communications biology 5 (1), 369, 2022
强制性开放获取政策: US National Institutes of Health, Wellcome Trust
Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma
I Schrauwen, BI Melegh, I Chakchouk, A Acharya, A Nasir, A Poston, ...
European Journal of Human Genetics 27 (6), 869-878, 2019
强制性开放获取政策: US National Institutes of Health, Hungarian Scientific Research Fund
Identification of novel L2HGDH mutation in a large consanguineous Pakistani family- a case report
MI Ullah, A Nasir, A Ahmad, GV Harlalka, W Ahmad, MJ Hassan, ...
BMC medical genetics 19, 1-5, 2018
强制性开放获取政策: UK Medical Research Council
ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment
T Bharadwaj, I Schrauwen, S Rehman, K Liaqat, A Acharya, APJ Giese, ...
European Journal of Human Genetics 30 (1), 22-33, 2022
强制性开放获取政策: US National Institutes of Health
Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment
E Wonkam-Tingang, I Schrauwen, KK Esoh, T Bharadwaj, ...
Genes 11 (11), 1249, 2020
强制性开放获取政策: US National Institutes of Health, Wellcome Trust
A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family
E Wonkam-Tingang, I Schrauwen, KK Esoh, T Bharadwaj, ...
Experimental Biology and Medicine 246 (13), 1524-1532, 2021
强制性开放获取政策: US National Institutes of Health, Wellcome Trust
A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
F Ahmad, I Ahmed, A Nasir, M Umair, S Shahzad, D Muhammad, ...
European Journal of Dermatology 28, 209-216, 2018
强制性开放获取政策: US National Institutes of Health
Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment
K Liaqat, S Hussain, M Bilal, A Nasir, A Acharya, RH Ali, S Nawaz, ...
Journal of human genetics 65 (2), 187-192, 2020
强制性开放获取政策: US National Institutes of Health
Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13
A Acharya, SI Raza, MZ Anwar, T Bharadwaj, K Liaqat, MAS Khokhar, ...
Journal of human genetics 66 (10), 1009-1018, 2021
强制性开放获取政策: US National Institutes of Health
Phenotype expansion for atypical Gaucher disease due to homozygous missense PSAP variant in a large consanguineous Pakistani family
K Liaqat, S Hussain, A Acharya, A Nasir, T Bharadwaj, M Ansar, S Basit, ...
Genes 13 (4), 662, 2022
强制性开放获取政策: US National Institutes of Health
A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family
N Manyisa, I Schrauwen, LA de Souza Rios, S Mowla, ...
Genes 12 (11), 1765, 2021
强制性开放获取政策: US National Institutes of Health, Wellcome Trust
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