 | ABCD1 is a protein that transfers fatty acids into peroxisomes. The protein encoded by this gene is a member of the superfamily of ATP-binding cassette... 10 KB (1,199 words) - 06:59, 18 December 2023 |
 | ALD is caused by mutations in ABCD1, located at Xq28 and demonstrates X-linked recessive inheritance. The gene ABCD1 encodes a peroxisomal membrane transporter... 35 KB (3,673 words) - 19:21, 19 February 2024 |
Archer-Daniels-Midland, Bunge, Cargill, Louis Dreyfus ABC (disambiguation) ABCD1, a protein ABCD2 score, a score for determining the risk of stroke after... 2 KB (283 words) - 09:03, 2 May 2024 |
the patient and genetically modified to carry a functional copy of the ABCD1 gene using a lentiviral vector. Patients undergo myeloablative chemotherapy... 20 KB (1,723 words) - 17:50, 28 February 2024 |
000 Adenylosuccinate lyase deficiency ADSL recessive Adrenoleukodystrophy ABCD1 (X) recessive 1:17,000 Alagille syndrome JAG1, NOTCH2 dominant 1:30,000-50... 42 KB (969 words) - 16:02, 3 April 2024 |
 | that encode half transporters expressed exclusively in the peroxisome. ABCD1 is responsible for the X-linked form of Adrenoleukodystrophy (ALD) which... 111 KB (14,398 words) - 16:45, 29 April 2024 |
 | acyltransferase deficiency 222765 GNPAT E80.315 X-linked adrenoleukodystrophy 300100 ABCD1 E71.33 α-Methylacyl-CoA racemase deficiency 604489 AMACR RCDP Type 2 222765... 8 KB (578 words) - 22:58, 29 April 2024 |
 | children using a lentivirus vector to deliver a functioning version of ABCD1, the gene that is mutated in the disorder. An April paper reported that... 172 KB (17,769 words) - 01:31, 8 May 2024 |
Steps, Tina Cousins, Cleopatra, B*Witched, Billie. Epic Records. 1999. ABCD1.{{cite AV media notes}}: CS1 maint: others in cite AV media (notes) (link)... 10 KB (689 words) - 01:10, 3 August 2023 |
HGNC:52 Q5T3U5 61 ABCC11 HGNC:14639 Q96J66 62 ABCC12 HGNC:14640 Q96J65 63 ABCD1 HGNC:61 P33897 64 ABCD2 HGNC:66 Q9UBJ2 65 ABCD3 HGNC:67 P28288 66 ABCD4... 277 KB (17 words) - 23:17, 27 April 2024 |