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Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct ...
Identified mutations of ABCD1. Mutations of ABCD1 gene were widely ...
Frontiers | Novel mutations in the ABCD1 gene caused ...
Novel ABCD1 Variants in X‐Linked Adrenoleukodystrophy - Dong - Clinical ...
A Novel Double Mutation in the ABCD1 Gene in a Patient with X-linked ...
Intrathecal delivery of nucleic acid sequences encoding abcd1 for ...
X‑linked adrenoleukodystrophy caused by maternal ABCD1 mutation and ...
Structure and Function of the ABCD1 Variant Database: 20 Years, 940 ...
S149R, a novel mutation in the ABCD1 gene causing X-linked ...
[PDF] Novel mutation in ATP-binding domain of ABCD1 gene in ...
Identification of Two Novel Mutations of ABCD1 Gene in Pedigrees with X ...
ABCD1 deletion‐induced mitochondrial dysfunction is corrected by SAHA ...
(PDF) Identification of two novel mutations of ABCD1 gene in pedigrees ...
(PDF) From gene to therapy: a review of deciphering the role of ABCD1 ...
(PDF) Structure and Function of the ABCD1 Variant Database: 20 Years ...
X Chromosome Inactivation (XCI) and ABCD1 Allele-Specific Expression ...
ABCD1 antibody (60153-1-Ig) | Proteintech
In-frame deletion variant of ABCD1 in a sporadic case of ...
ABCD1 allele-specific expression in skin fibroblasts. (A) Distribution ...
Abcd1 deficiency accelerates cuprizone-induced oligodendrocyte loss and ...
(PDF) Abcd1 deficiency accelerates cuprizone-induced oligodendrocyte ...
(PDF) Two Single Nucleotide Deletions in the ABCD1 Gene Causing ...
Silencing of Abcd1 and Abcd2 genes sensitizes astrocytes for ...
61 different ABCD1 variants in 68 X‐ALD families. aNovel variants are ...
Novel mutation in ATP-binding domain of ABCD1 gene in ...
ABCD1 gene primers sequences | Download Table
(PDF) A novel mutation in the ABCD1 gene of a patient with X-linked ...
Gene expression profile of the human ABCD1 and ABCD2 genes. Comparison ...
ABCD1 deletion-induced mitochondrial dysfunction is corrected by SAHA ...
[PDF] A novel ABCD1 gene mutation in a patient with X-linked ...
Overall structure of ABCD1 in complex with C26:0 fatty acid. a, b ...
ABCD1 mutations and the X‐linked adrenoleukodystrophy mutation database ...
(PDF) A novel mutation in the ABCD1 gene of a Moroccan patient with X ...
(PDF) Molecular analysis of ABCD1 gene in Indian patients with X-linked ...
Schematic representation of the 10 exons of ABCD1 gene. Amino acid ...
Novel ABCD1 Variants in X‐Linked Adrenoleukodystrophy
(PDF) X‑linked adrenoleukodystrophy caused by maternal ABCD1 mutation ...
Novel ABCD1 mutation detected in a symptomatic female carrier of ...
The ABCD1 mutations identified in patients with ataxia. (A-B) The ...
Proposed model for the roles of ABCD1 and ABCD2 transporters in fatty ...
ABCD1 Gene - GeneCards | ABCD1 Protein | ABCD1 Antibody
(PDF) Identification of Two Novel Mutations of ABCD1 Gene in Pedigrees ...
The ABCD1 gene
ABCD2 gene expression remains at low levels compared to ABCD1 after ...
Therapeutic effects of normal cells on ABCD1 deficient cells in vitro ...
ABCD1 - Wikipedia
The upregulation of ABCD1 in human macrophages entering... | Download ...
(PDF) S149R, a novel mutation in the ABCD1 gene Causing X-linked ...
The evolutionary conservation of each amino acid within the ABCD1 ...
ABCD1 Transporter Deficiency Results in Altered Cholesterol Homeostasis
ABCD1 antibody
ABCD1 过氧化物酶体网络和突变诱导的网络扰动的 iBRET 屏幕,Journal of Proteome Research - X-MOL
(PDF) Preferential expression of mutant ABCD1 allele is common in ...
Adrenoleukodystrophy ABCD1 Disease X-linked recessive inheritance ...
ABCD1 antibody - BiCell Scientific®
AAV9-mediated ABCD1 expression in mixed brain glial cell culture from ...
Protein Interactions - ABCD1 GENE AND ALD
(PDF) Structures of the human peroxisomal fatty acid transporter ABCD1 ...
ABCD1 antibody (83038-4-RR) | Proteintech
ABCD1 molecular model for full-length human sequence for variant ...
中国科大揭示人类超长链脂酰辅酶A跨膜转运蛋白ABCD1的底物识别与转运机制-中国科大新闻网
Substrate Specificity and the Direction of Transport in the ABC ...
Pathophysiology of X-Linked Adrenoleukodystrophy: Mutations in the ...
Abcd1/Abcd2 silencing induces expression and DNA binding of NF-kB, AP1 ...
Contiguous Deletion of the X-Linked Adrenoleukodystrophy Gene (ABCD1 ...
Secondary failure of lentiviral vector gene therapy in a cerebral ...
Frontiers | A case of adrenomyeloneuropathy caused by a novel point ...
Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in ...
Experimental and Therapeutic Medicine
Frontiers | Exploratory study of autophagy inducer sirolimus for ...
Method for treating adrenoleukodystrophy (ALD) through optimized ...
Brainstem dominant form of X‐linked adrenoleukodystrophy with a novel ...
Impaired Very Long-chain Acyl-CoA β-Oxidation in Human X-linked ...
(PDF) An Incidentally Identified Sporadic Case with ...
(PDF) Peroxisomal ABC transporters and X-linked adrenoleukodystrophy
Central precocious puberty in a boy with X-linked adrenoleukodystrophy ...
Substrate specificity of the ABCD transporters. ABCD1–3 predominately ...
Targeting ABCD1-ACOX1-MET/IGF1R axis suppresses multiple myeloma - PMC
Targeting and localization of the ABCD transporters. For the ...
Oxidative stress, myelin, and axonal pathologies in 22-month-old Abcd1− ...
ATPase activities of reconstituted ABCD1. (A) Purified His-ABCD1 ...
of ABCB1 regulation by developmental signaling pathways in cancer. The ...
Targeted Brain Delivery of Dendrimer-4-Phenylbutyrate Ameliorates ...
Segregation of identified mutations in the AARS2, ABCD1, CSF1R, and ...
Structural basis of substrate recognition and translocation by human ...
Illustration of an X chromosome with labels for genes Dystrophin, FMR1 ...
(PDF) Structural basis of substrate recognition and translocation by ...
A Korean boy with atypical X-linked adrenoleukodystrophy confirmed by ...
ABCD proteins
