INVESTIGADORES
WALZ Katherina
congresos y reuniones científicas
WALZ, KATHERINA; TEKIN, MUSTAFA
A recessive variant in forkhead box domain of FOXF2 is associated with profound hearing loss and inner ear anomaly.
The 67th Annual Meeting of the American Society of Human Genetics (ASHG)
Lugar: Orlando; Año: 2017;
WALZ, KATHERINA; YOUNG, JUAN I.
Behavioral Characterization in a Mouse Model of Bohring?Opitz Syndrome.
The 67th Annual Meeting of the American Society of Human Genetics (ASHG)
Lugar: Orlando; Año: 2017;
WALZ, KATHERINA
Molecular mechanisms underlying phenotypic outcomes of copy number variation
Jim Lupski's 30th Anniversary
Año: 2017;
WALZ, KATHERINA
The mouse model for PTLS
4th Annual Potocki-Lupski Syndrome (PTLS) Family Conference
Lugar: Houston; Año: 2017;
WALZ, KATHERINA; YOUNG, JUAN I.
Rai1 haploinsufficient mice exhibit abnormal social behavior
The 65th Annual Meeting of the American Society of Human Genetics (ASHG)
Lugar: Maryland; Año: 2015;
WALZ, KATHERINA; TEKIN, MUSTAFA
Genomic approach identifies novel proteins necessary for inner ear function and development across multiple species.
The 64th Annual Meeting of the American Society of Human Genetics (ASHG)
Lugar: San Diego; Año: 2014;
WALZ, KATHERINA; TEKIN, MUSTAFA
The Ankrd11 mutation in the Yoda mouse mirrors the human gene defect and provides new insights into KBG syndrome.
The 64th Annual Meeting of the American Society of Human Genetics (ASHG)
Año: 2014;
WALZ, KATHERINA; YOUNG, JUAN I.
Rai1 dosage in early development is essential to PTLS-like phenotype development in Dt-Rai1 animals.
The American Society of Human Genetics
Año: 2013;
WALZ, KATHERINA
Pathogenesis Study of PTLS Like Phenotypes in I-Rai1 Mice.
Annual Biomedical Research Conference for Minority Students (ABRCMS).
Año: 2013;
WALZ, KATHERINA
Different subcellular localization of a mutant form of Ankrd11 associated with KBG Syndrome.
SACNAS National conference
Año: 2013;
WALZ, KATHERINA
Transcription Factor Activity is Impaired in Mutants Associated with Smith-Magenis Syndrome.
PRISM research Conference,
Lugar: Denver; Año: 2012;
WALZ, KATHERINA; YOUNG, JUAN I.
RAI1: Molecular and functional studies to understand its relationship to Neurobehavioral Alterations.
ASHG Annual Meeting
Año: 2012;
WALZ, KATHERINA
The Calcium Channel TRPC6, Known to Cause FSGS when Chronically Hyperactive, Protects Podocytes from Acute Complement-Mediated Injury
ASN kidney week
Año: 2012;
WALZ, KATHERINA
Janus-headed TRPC6: the calcium channel, known to cause FSGS when chronically hyperactive, protects podocytes from acute complement-mediated injury.
9th International Podocyte Conference
Año: 2012;
WALZ, KATHERINA; LUPSKI, JAMES R.
A duplication CNV that protects against metabolic syndrome.
The 12th International Congress of Human Genetics (ICHG) and the 61st Annual Meeting of the American Society of Human Genetics (ASHG),
Año: 2011;
WALZ, KATHERINA
Genetics Awareness Project (GAP) promotes genetics education and genomic research participation in under-represented racial-ethnic groups in South Florida.
The 12th International Congress of Human Genetics (ICHG) and the 61st Annual Meeting of the American Society of Human Genetics (ASHG),
Año: 2011;
WALZ, KATHERINA
Evaluation of Molecular Pathway Associated with FSGS and Trpc6 Mutation.
Annual Biomedical Research Conference for Minority Students (ABRCMS)
Año: 2011;
WALZ, KATHERINA
La sobreexpresión tubular de gramlin en un raton transgénico induce mayor suceptibilidad a proteinuria y daño tubuli-instrersticial en modelos de daño agudo por acido folico.
Congreso conjunto de las Sociedades de Nefrología, Hipertensión y Transplante
Año: 2010;
WALZ, KATHERINA
Chromosome-wide mapping of long-range interactions involved in Smith-Magenis and Potocki-Lupski syndromes.
ASHG Annual Meeting
Año: 2010;
WALZ, KATHERINA
Generation of transgenic mice expressing human Gremlin to determine its pathological role in kidney fibrosis.
ISN for the Nexus Symposium on Fibrosis and the Kidney
Año: 2010;
