Results 131 to 140 of about 28,396 (290)

Microhaplotype Methods Enable Relationship Inference in a Bottlenecked Mammalian Species

open access: yesAnimal Conservation, EarlyView.
Northern elephant seals (Mirounga angustirostris) are among the most genetically depauperate mammals in the world. A near‐total population bottleneck in the 19th century, coupled with the breeding system of extreme polygyny, has challenged efforts to estimate individual reproductive success with genetic methods.
Keith M. Hernandez   +6 more
wiley   +1 more source

Development and Validation of Tetranucleotide Repeat Microsatellite Markers at the Whole-Genome Level in the Yangtze Finless Porpoise [PDF]

open access: gold
Meng‐Ting Tang   +10 more
openalex   +1 more source

Robust Preimplantation Genetic Testing of Huntington Disease by Combined Triplet-Primed PCR Analysis of the HTT CAG Repeat and Multi-Microsatellite Haplotyping [PDF]

open access: gold, 2019
Mingjue Zhao   +6 more
openalex   +1 more source

Epigenome editing of microsatellite repeats defines tumor-specific enhancer functions and dependencies. [PDF]

open access: yesGenes Dev, 2018
Boulay G   +6 more
europepmc   +1 more source

Inheritance and diversity of simple sequence repeat (SSR) microsatellite markers in various families of Picea abies [PDF]

open access: bronze, 2003
Reza Yazdani   +4 more
openalex   +1 more source

Covalent drug discovery: Progress against key targets, emerging strategies and lessons learnt

open access: yesBritish Journal of Pharmacology, EarlyView.
Abstract Covalent drug discovery is currently experiencing a boom in industrial and academic interest. To date, at least 75 covalent drugs have received regulatory approval, targeting both traditional target classes and more challenging proteins for which other approaches failed. In many cases, unique aspects of covalent targeting are essential for the
Charles P. Brown   +2 more
wiley   +1 more source

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site. [PDF]

open access: bronze, 1991
Robert I. Richards   +8 more
openalex   +1 more source

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

open access: yesClinical Genetics, EarlyView.
The frequency and severity of congenital heart disease vary extensively in individuals with 22q11.22–23 distal deletions. Reduced gene dosage particularly within the low copy repeat (LCR22) D–E region including MAPK1 and HIC2 conveys risk for these defects.
Tanner J. Nelson   +22 more
wiley   +1 more source

An A13 Repeat within the 3′-Untranslated Region of Epidermal Growth Factor Receptor (EGFR) Is Frequently Mutated in Microsatellite Instability Colon Cancers and Is Associated with Increased EGFR Expression [PDF]

open access: bronze, 2009
Ziqiang Yuan   +15 more
openalex   +1 more source

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