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Jean-Pierre Adam (born 1956) is an American
human geneticist, currently an associate director at the Intellectual
and Developmental Disabilities Research Center (1995), and professor at
the Department of Molecular and Human Genetics at Baylor College of
Medicine BCM since 1999. Since 2018, he is the director at the Cancer
and Cell L'arte di costruire presso i romani. Materiali e tecniche.
Ediz. illustrata Biology Ph.D program, and the director of Integrative
Molecular and Biomedical Sciences Ph.D since 2015 at BMC.[1][2]
Nelson received a bachelor's degree from the University of
Virginia in 1978 and received his PhD in molecular genetics from the
Massachusetts Institute of Technology in 1984. He carried out his
postdoctoral training L'arte di costruire presso i romani. Materiali e
tecniche. Ediz. illustrata at Massachusetts Institute of Technology
(1984–1985) and National Institutes of Health before moving to Baylor
College of Medicine.
Nelson joined the MIT Center for Cancer Research (CCR)
group of David Housman at the Massachusetts Institute of Technology as a
postdoctoral trainee (1986–1989). Nelson's work using introduced
selectable genes expanded approaches L'arte di costruire presso i
romani. Materiali e tecniche. Ediz. illustrata to whole human genome
mapping. From 1984 to 1985, in
an intramural National Institutes of
Health program at the laboratory of Robert Lazzarini, Nelson studied
neuroscience and defined genes encoding neurofilament proteins. In 1986
he joined the C. Thomas Caskey laboratory at the Institute of Molecular
Genetics, Baylor College of L'arte di costruire presso i romani.
Materiali e tecniche. Ediz. illustrata Medicine.[3]
Applying the Polymerase chain reaction PCR, a technique
that allows rapid gene mapping and isolation of specific chromosomal
regions, Nelson et al. identified chromosomal locations of large
fragments of the human X chromosome;[4] Nelson contributed to the human,
mouse and fly reference sequences and was a co-discoverer of the L'arte
di costruire presso i romani. Materiali e tecniche. Ediz. illustrata
mutation that causes Fragile X syndrome as an expansion of a
trinucleotide repeat in the FMR1 gene.[5] Nelson's contributions have
led to the description of Lowe syndrome,[6] and the identification of
FMR2 for FRAXE syndrome.[7]
Nelson's molecular techniques led to the development of
genome mapping and sequencing and discovery of L'arte di costruire
presso i romani. Materiali e tecniche. Ediz. illustrata disease genes,
contributing efforts to map and sequence of the human X chromosome. He
was a leader in genetic and
genomic analyses across all species.[4][8][9][10]
With a group of international collaborators, Nelson's
research group was able to identify a recurrent, homology-driven
deletion in the NEMO gene in Incontinentia pigmenti (IP), L'arte di
costruire presso i romani. Materiali e tecniche. Ediz. illustrata an
X-linked genetic disease.[11][12][13][14]
[15]
Nelson and other collaborators at BMC, Emory University,
and Erasmus University Rotterdam identified a massive expansion of CGG
repeat (Trinucleotide repeat disorder) in FMR1. This was the first to be
identified as the underlying mutations in human genetic disorders.
Their findings in FMR1 explained the unusual L'arte di costruire presso i
romani. Materiali e tecniche. Ediz. illustrata inheritance in Fragile X
syndrome and provided the principles for all subsequent unstable repeat
disorders such as myotonic dystrophy, Huntington's disease, and
amyotrophic lateral sclerosis.[5][16][17][18]
By studying humans, mice, flies and yeast Nelson's research
group has characterized the origins of instability in the repeat, the
consequences of "premutation" length expansions, L'arte di costruire
presso i romani. Materiali e tecniche. Ediz. illustrata and the function
of FMR1 and related FXR1 and FXR2. Nelson and his research group have
defined roles for FMR1 and paralogs in circadian rhythm, energy
metabolism, neuronal stem cell
development, and microRNA function.
Their research results are being used in research to define the role of
FMR1 in development L'arte di costruire presso i romani. Materiali e
tecniche. Ediz. illustrata and potential treatment for these diseases in
adulthood.[19][20][21][22][23]
FXTAS individuals are cognitively unaffected until they
reach their 60 or 70, when they show neural degeneration and nuclear
inclusions during autopsy. Nelson's research group has used flies and
mice to identify and characterize modifiers that showed that the CGG
repeat is L'arte di costruire presso i romani. Materiali e tecniche.
Ediz. illustrata necessary and sufficient to affect mammalian neurons.
Models developed by Nelson's research group have improved the
understanding of mechanisms of this disease, including a role for
RNA-binding functions such as TDP-43 and alterations in
5-Hydroxymethylcytosine.[24][25][26][27]
Nelson is a member of the Board of Directors of the
American Society of Human L'arte di costruire presso i romani. Materiali
e tecniche. Ediz. illustrata Genetics, was its President in 2018, and
served as Secretary from 2003 to 2009.
Nelson has served in many advisory boards and committees, including FRAXA Research Foundation Advisory Board (1999–prese
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