You are here
JS GENETICS, LLC
UEI: N/A
# of Employees: N/A
HUBZone Owned: No
Socially and Economically Disadvantaged: No
Woman Owned: No
Award Charts
Award Listing
-
Identification of Oligodendrocyte Stimulators
Amount: $708,235.00DESCRIPTION (provided by applicant): Oligodendrocytes (OLs) are the myelinating cells of the central nervous system and play a critical role in white matter formation. Serious clinical disorders affec ...
SBIRPhase II2010Department of Health and Human Services National Institutes of Health -
Development of Novel Diagnostics for Fragile X Syndrome
Amount: $1,069,800.00DESCRIPTION (provided by applicant): Fragile X Syndrome (FRAX) is the most common genetic cause of mental retardation in males. FRAX is caused by the expansion of a CGG trinucleotide repeat of the ...
SBIRPhase II2010Department of Health and Human Services National Institutes of Health -
Development of Novel Diagnostics for Fragile X Syndrome
Amount: $117,700.00DESCRIPTION (provided by applicant): Fragile X Syndrome (FRAX), is the most common cause of mental retardation in males. The incidence of FRAX is 1 per 4000 in males and 1 per 8000 in females. FRAX i ...
SBIRPhase I2008Department of Health and Human Services National Institutes of Health -
Identification of Oligodendrocyte Stimulators
Amount: $150,854.00DESCRIPTION (provided by applicant): Abstract Oligodendrocytes (OLs) are the myelinating cells of the central nervous system and play a critical role in white matter formation and white matter stabili ...
SBIRPhase I2008Department of Health and Human Services National Institutes of Health -
Molecular Diagnosis of Dyslexia
Amount: $122,164.00DESCRIPTION (provided by applicant): Reading disability (RD), also known as dyslexia, is the most common learning disability affecting school children. In the US, Canada, Europe and countries where it ...
SBIRPhase I2007Department of Health and Human Services National Institutes of Health -
Newborn Screening for Sex Chromosome Disorders
Amount: $464,396.00DESCRIPTION (provided by applicant): Turner syndrome (TS) is the most common genetic problem affecting women and occurs when an entire, or a portion of an X-chromosome is deleted. The incidence of TS ...
STTRPhase II2007Department of Health and Human Services National Institutes of Health -
Newborn Screening for Sex Chromosome Disorders
Amount: $129,953.00DESCRIPTION (provided by applicant): Turner syndrome (TS) is the most common genetic problem effecting women, with an incidence of 1 in 1,500 to 2,000 live female births and occurs when an entire, or ...
STTRPhase I2006Department of Health and Human Services National Institutes of Health -
Newborn Screening for Sex Chromosome Disorders
Amount: $129,953.00DESCRIPTION (provided by applicant): Turner syndrome (TS) is the most common genetic problem effecting women, with an incidence of 1 in 1,500 to 2,000 live female births and occurs when an entire, ...
SBIRPhase I2006Department of Health and Human Services National Institutes of Health
