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■ Search Result - Abbreviation : CMT1

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Abbreviation: CMT1
Appearance Frequency: 100 time(s)
Long forms: 10

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
Charcot-Marie-Tooth disease type 1
(47 times)
Neurology
(30 times)
PMP22 (15 times)
HNPP (9 times)
HMSN I (8 times)
1988 DNA probes in Charcot-Marie-Tooth neuropathy.
Charcot-Marie-Tooth type 1
(19 times)
Genetics, Medical
(9 times)
HNPP (5 times)
PMP22 (5 times)
CMT1A (3 times)
1994 Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene.
Charcot-Marie-Tooth neuropathy type 1
(13 times)
Neurology
(6 times)
PMP22 (8 times)
HNPP (6 times)
CMT2 (5 times)
1988 Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type I.
CMT type 1
(11 times)
Genetics, Medical
(4 times)
CMT (11 times)
CMT2 (7 times)
PMP22 (4 times)
1993 Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication.
Charcot-Marie-Tooth type 1 disease
(5 times)
Neurology
(3 times)
HNPP (2 times)
CHN (1 time)
CMT (1 time)
1997 Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent.
Chloroplast manganese transporter 1
(1 time)
PAM71 (1 time)
PML3 (1 time)
2020 Homologous Proteins of the Manganese Transporter PAM71 Are Localized in the Golgi Apparatus and Endoplasmic Reticulum.
CHLOROPLAST MANGANESE TRANSPORTER1
(1 time)
Botany
(1 time)
Mn (1 time)
PAM71 (1 time)
PSII (1 time)
2018 The Plastid Envelope CHLOROPLAST MANGANESE TRANSPORTER1 Is Essential for Manganese Homeostasis in Arabidopsis.
Chromomethylase 1
(1 time)
Epigenesis, Genetic
(1 time)
EK (1 time)
2018 CMT3 and SUVH4/KYP silence the exonic Evelknievel retroelement to allow for reconstitution of CMT1 mRNA.
ciliary muscle thicknesses at 1 mm
(1 time)
Ophthalmology
(1 time)
SPHEQ (1 time)
2013 Region-specific relationships between refractive error and ciliary muscle thickness in children.
10  classifications: type 1, the demyelinating form
(1 time)
Nervous System Diseases
(1 time)
CMT (1 time)
2006 Charcot-marie-tooth disease: seventeen causative genes.