• Thumbnail for Machado–Joseph disease
    MachadoJoseph disease (MJD), also known as MachadoJoseph Azorean disease, Machado's disease, Joseph's disease or spinocerebellar ataxia type 3 (SCA3)...
    22 KB (2,328 words) - 12:19, 5 November 2023
  • Thumbnail for Groote Eylandt
    Coolsteerdt. However, the relative prevalence of the hereditary Machado-Joseph Disease (MJD) in the Groote Eylandt community (a condition otherwise mainly...
    20 KB (1,777 words) - 22:46, 11 May 2024
  • Thumbnail for Rheobase
    neurological pathologies, including diabetic neuropathy, CIDP, MachadoJoseph disease, and ALS. The strength-duration time constant (chronaxie) and rheobase...
    28 KB (3,518 words) - 10:35, 11 April 2024
  • MJD may refer to: Modified Julian Date, see Julian day § Variants MachadoJoseph disease Maurice Jones-Drew, former NFL running back Mizo Janata Dal, an...
    356 bytes (72 words) - 02:49, 14 March 2022
  • R S T U V W X Y Z This list contains acronyms and initials related to diseases (infectious or non-infectious) and medical disorders. Acronyms in healthcare...
    28 KB (112 words) - 15:27, 5 May 2024
  • Thumbnail for Ataxin 3
    Ataxin-3 is a protein that in humans is encoded by the ATXN3 gene. MachadoJoseph disease, also known as spinocerebellar ataxia-3, is an autosomal dominant...
    10 KB (1,245 words) - 11:46, 28 December 2023
  • Thumbnail for Truncal ataxia
    viral cerebellar ataxia Gerstmann–Sträussler–Scheinker syndrome MachadoJoseph disease Microcephaly N-acetylaspartate deficiency Neuhauser–Eichner–Opitz...
    4 KB (254 words) - 23:03, 29 January 2024
  • Thumbnail for Chromosome 14
    AHNAK2: encoding protein Ahnak nucleoprotein 2 ATXN3: Ataxin-3 (Machado-Joseph disease) BCL2L2: encoding the anti-apoptotic protein Bcl-w of the Bcl-2...
    26 KB (1,831 words) - 14:23, 31 March 2024
  • Thumbnail for Slipped strand mispairing
    spinocerebellar ataxia type 1 ( trinucleotide expansion in the SCA1gene), Machado-Joseph disease ( trinucleotide expansion in the SCA3 gene), myotonic dystrophy...
    10 KB (1,175 words) - 10:11, 22 March 2024
  • disease is named after a patient, examples being Lou Gehrig disease, Hartnup disease, and Mortimer disease. In one instance, MachadoJoseph disease,...
    62 KB (6,446 words) - 06:48, 31 March 2024
  • Thumbnail for Spinocerebellar ataxia
    Spinocerebellar ataxia (category Rare diseases)
    NIH/UW GeneTests sca2 at NIH/UW GeneTests sca3 at NIH/UW GeneTests machado_joseph at NINDS sca6 at NIH/UW GeneTests sca7 at NIH/UW GeneTests sca8 at NIH/UW...
    36 KB (2,931 words) - 20:04, 1 May 2024
  • Thumbnail for Olivopontocerebellar atrophy
    ataxia (such as the hereditary spinocerebellar ataxia known as MachadoJoseph disease) and multiple system atrophy (MSA), with which it is primarily associated...
    8 KB (731 words) - 14:37, 27 October 2023
  • Thumbnail for Makassan contact with Australia
    across Australia from Sydney Cove. The prevalence of the hereditary MachadoJoseph disease in the Groote Eylandt community has been attributed to outside contact...
    39 KB (4,232 words) - 04:12, 12 May 2024
  • spinal stenosis Lupus erythematosus – neurological sequelae Lyme disease MachadoJoseph disease Macrencephaly Macrocephalia Macropsia Mal de debarquement Megalencephalic...
    13 KB (1,147 words) - 05:51, 17 May 2024
  • cause SCA2 with polyglutamine expansion. Ataxin 3, coded by ATXN3. Machado-Joseph disease is caused by polyglutamine expansions in ataxin 3. Ataxin 7, coded...
    2 KB (199 words) - 11:54, 17 October 2022
  • Thumbnail for Cerebellum
    cerebellum may be absent. The inherited neurological disorders MachadoJoseph disease, ataxia telangiectasia, and Friedreich's ataxia cause progressive...
    94 KB (11,561 words) - 12:49, 7 May 2024
  • trinucleotide repeat disorders, a subset of microsatellite expansion diseases (also known as repeat expansion disorders), are a set of over 30 genetic...
    23 KB (2,477 words) - 06:38, 27 April 2024
  • Thumbnail for Small interfering RNA
    2015), amyloid lateral sclerosis (ALS) (Schwarz et al. 2006), and MachadoJoseph disease (Alves et al. 2008). Their therapeutic potential has also been assessed...
    55 KB (6,760 words) - 11:46, 28 April 2024
  • Thumbnail for Ubiquitin-interacting motif
    multi-ubiquitin binding subunit of the 26S proteasome. Vertebrate Machado-Joseph disease protein 1 (Ataxin-3), which acts as a histone-binding protein that...
    6 KB (604 words) - 06:36, 26 April 2024
  • Thumbnail for SDD-AGE
    combinatorial approach to identify calpain cleavage sites in the Machado-Joseph disease protein ataxin-3". Brain. 140 (5): 1280–1299. doi:10.1093/brain/awx039...
    6 KB (709 words) - 23:29, 15 February 2024
  • Thumbnail for Sephardic Jews
    dehydrogenase deficiency and Gilbert's Syndrome Glycogen storage disease type III Machado-Joseph disease 1906 – Henri Moissan, Chemistry 1911 - Tobias Asser, Peace...
    172 KB (19,805 words) - 05:02, 28 April 2024
  • Thumbnail for Genetically modified animal
    PMID 26613986. Schmidt J, Schmidt T (2018). "Animal Models of Machado-Joseph Disease". Polyglutamine Disorders. Advances in Experimental Medicine and...
    102 KB (11,039 words) - 09:40, 9 May 2024
  • at the University of the Azores, where she conducted her PhD on "Machado-Joseph disease: from genetic variability to clinical heterogeneity". She then trained...
    6 KB (484 words) - 19:33, 20 March 2024
  • Thumbnail for Genetically modified organism
    PMID 26613986. Schmidt J, Schmidt T (2018). "Animal Models of Machado-Joseph Disease". Polyglutamine Disorders. Advances in Experimental Medicine and...
    222 KB (24,527 words) - 20:35, 30 April 2024
  • Guilherme Karan (category Deaths from neurodegenerative disease)
    since the time of the assault Karam began to manifest symptoms of Machado-Joseph disease, a degenerative syndrome, also known as spinocerebellar ataxia type...
    7 KB (516 words) - 17:41, 5 May 2024
  • Thumbnail for Anindilyakwa people
    The genetic presence of MachadoJoseph disease in 4 families is thought to derive from a Makassar ancestor who carried the disease. Several Macassan words...
    19 KB (1,934 words) - 13:53, 12 May 2024
  • Thumbnail for Autosomal dominant cerebellar ataxia
    with SCA3 being the most common subtype of all of Type 1. SCA3, Machado-Joseph disease, is the most common because the mutation repeats more than 56 times...
    14 KB (1,560 words) - 17:28, 28 April 2024
  • Thumbnail for Anindilyakwa language
    Anindilyakwa man, Steve 'Bakala' Wurramara, who is afflicted with Machado-Joseph Disease (MJD), a hereditary neurodegenerative disorder that results in a...
    26 KB (1,541 words) - 06:05, 17 March 2024
  • spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease-causing mutations". Journal of Neurology. 248...
    6 KB (746 words) - 23:24, 18 August 2023
  • Thumbnail for MARCH5
    associated with specific neurodegenerative disorders such as ataxin-3 in MachadoJoseph disease or mSOD1 in amyotrophic lateral sclerosis likely supporting mitochondrial...
    10 KB (1,266 words) - 12:41, 26 April 2024