cytosine and Atrophy studies

cytosine and Atrophy

cytosine has been researched along with Atrophy in 4 studies

Atrophy: Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes.

Research Excerpts

Excerpt	Relevance	Reference
"Two families with frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17) resulting from the microtubule associated protein tau (MAPT) gene IVS10+16C>T splice site mutation are reported, members of which showed variable clinical phenotypes at presentation."	1.35	Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation. ( Larner, AJ, 2009)

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (25.00)	18.2507
2000's	3 (75.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Timeframe

Studies, this research(%)

All Research%

pre-1990

0 (0.00)

18.7374

1990's

1 (25.00)

18.2507

2000's

3 (75.00)

29.6817

2010's

0 (0.00)

24.3611

2020's

0 (0.00)

2.80

Authors

Authors	Studies
Larner, AJ	1
Wang, L	1
Damji, KF	1
Chialant, D	1
Hodge, WG	1
Chhetri, DK	1
Jahan-Parwar, B	1
Hart, SD	1
Bhuta, SM	1
Berke, GS	1
Shapiro, NL	1
Jönsson, E	1
Brené, S	1
Lindblad, K	1
Sharara, S	1
Sedvall, G	1
Schalling, M	1

Studies

Larner, AJ

Wang, L

Damji, KF

Chialant, D

Hodge, WG

Chhetri, DK

Jahan-Parwar, B

Hart, SD

Bhuta, SM

Berke, GS

Shapiro, NL

Jönsson, E

Brené, S

Lindblad, K

Sharara, S

Sedvall, G

Schalling, M

Other Studies

4 other studies available for cytosine and Atrophy

Article	Year
Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation. Journal of the neurological sciences, 2009, Dec-15, Volume: 287, Issue:1-2 Topics: Atrophy; Base Sequence; Brain; Brain Chemistry; Cytosine; Disease Progression; DNA; DNA Mutational A	2009
Hypotony after intravenous cidofovir therapy for the treatment of cytomegalovirus retinitis. Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, 2002, Volume: 37, Issue:7 Topics: AIDS-Related Opportunistic Infections; Antiviral Agents; Atrophy; Child; Cidofovir; Ciliary Body; Cy	2002
Local and systemic effects of intralaryngeal injection of cidofovir in a canine model. The Laryngoscope, 2003, Volume: 113, Issue:11 Topics: Animals; Antiviral Agents; Atrophy; Blood Urea Nitrogen; Cidofovir; Creatinine; Cytosine; Dogs; Dose	2003
Lack of expansion of cytosine adenine guanine trinucleotide repeat in the dentatorubral and pallidoluysian atrophy gene in Swedish schizophrenic patients. Biological psychiatry, 1996, Aug-01, Volume: 40, Issue:3 Topics: Adenine; Alleles; Atrophy; Autoradiography; Chromosomes, Human, Pair 13; Cytosine; Dentate Gyrus; Gl	1996

Article

Year

Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation.

Journal of the neurological sciences, 2009, Dec-15, Volume: 287, Issue:1-2

Topics: Atrophy; Base Sequence; Brain; Brain Chemistry; Cytosine; Disease Progression; DNA; DNA Mutational A

2009

Hypotony after intravenous cidofovir therapy for the treatment of cytomegalovirus retinitis.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, 2002, Volume: 37, Issue:7

Topics: AIDS-Related Opportunistic Infections; Antiviral Agents; Atrophy; Child; Cidofovir; Ciliary Body; Cy

2002

Local and systemic effects of intralaryngeal injection of cidofovir in a canine model.

The Laryngoscope, 2003, Volume: 113, Issue:11

Topics: Animals; Antiviral Agents; Atrophy; Blood Urea Nitrogen; Cidofovir; Creatinine; Cytosine; Dogs; Dose

2003

Lack of expansion of cytosine adenine guanine trinucleotide repeat in the dentatorubral and pallidoluysian atrophy gene in Swedish schizophrenic patients.

Biological psychiatry, 1996, Aug-01, Volume: 40, Issue:3

Topics: Adenine; Alleles; Atrophy; Autoradiography; Chromosomes, Human, Pair 13; Cytosine; Dentate Gyrus; Gl

1996