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Melanie Lacaria

Showing results (1-10 of 19) with videos related to

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American Journal of Medical Genetics. Part A|May 25, 2013
Circadian abnormalities in mouse models of Smith-Magenis syndrome: evidence for involvement of RAI1Melanie Lacaria, Wenli Gu, James R Lupski
Adipocyte|May 24, 2013
A functional role for structural variation in metabolismMelanie Lacaria, Wenli Gu, James R Lupski
Cancer Genetics|October 14, 2017
A rare case of pediatric lipoma with t(9;12)(p22;q14) and evidence of HMGA2-NFIB gene fusionMelanie Lacaria, Dina El Demellawy, Jean McGowan-Jordan
Human Molecular Genetics|April 12, 2012
Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traitsMelanie Lacaria, Corinne Spencer, Wenli Gu, et al.
Parkinsonism & Related Disorders|June 19, 2025
First case of Cayman ataxia far north of the Caribbean: A 20-year-old Inuit male with homozygous deletion in ATCAY geneMarta Villa-Lopez, Melissa J MacPherson, Georges Maire, et al.
Parkinsonism & Related Disorders|November 6, 2025
Reprint of : First case of Cayman ataxia far north of the Caribbean: A 20-year-old Inuit male with homozygous deletion in ATCAY geneMarta Villa-Lopez, Melissa J MacPherson, Georges Maire, et al.
American Journal of Human Genetics|October 11, 2011
Frequency of nonallelic homologous recombination is correlated with length of homology: evidence that ectopic synapsis precedes ectopic crossing-overPengfei Liu, Melanie Lacaria, Feng Zhang, et al.
American Journal of Medical Genetics. Part A|September 20, 2012
Opposing phenotypes in mice with Smith-Magenis deletion and Potocki-Lupski duplication syndromes suggest gene dosage effects on fluid consumption behaviorDetlef H Heck, Wenli Gu, Ying Cao, et al.
Cell Reports|June 28, 2016
Notch Signaling Rescues Loss of Satellite Cells Lacking Pax7 and Promotes Brown Adipogenic DifferentiationAlessandra Pasut, Natasha C Chang, Uxia Gurriaran-Rodriguez, et al.
American Journal of Medical Genetics. Part A|April 23, 2017
Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feetMelanie Lacaria, Myriam Srour, Jacques L Michaud, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|May 25, 2013
Circadian abnormalities in mouse models of Smith-Magenis syndrome: evidence for involvement of RAI1Melanie Lacaria, Wenli Gu, James R Lupski
Adipocyte|May 24, 2013
A functional role for structural variation in metabolismMelanie Lacaria, Wenli Gu, James R Lupski
Cancer Genetics|October 14, 2017
A rare case of pediatric lipoma with t(9;12)(p22;q14) and evidence of HMGA2-NFIB gene fusionMelanie Lacaria, Dina El Demellawy, Jean McGowan-Jordan
Human Molecular Genetics|April 12, 2012
Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traitsMelanie Lacaria, Corinne Spencer, Wenli Gu, et al.
Parkinsonism & Related Disorders|June 19, 2025
First case of Cayman ataxia far north of the Caribbean: A 20-year-old Inuit male with homozygous deletion in ATCAY geneMarta Villa-Lopez, Melissa J MacPherson, Georges Maire, et al.
Parkinsonism & Related Disorders|November 6, 2025
Reprint of : First case of Cayman ataxia far north of the Caribbean: A 20-year-old Inuit male with homozygous deletion in ATCAY geneMarta Villa-Lopez, Melissa J MacPherson, Georges Maire, et al.
American Journal of Human Genetics|October 11, 2011
Frequency of nonallelic homologous recombination is correlated with length of homology: evidence that ectopic synapsis precedes ectopic crossing-overPengfei Liu, Melanie Lacaria, Feng Zhang, et al.
American Journal of Medical Genetics. Part A|September 20, 2012
Opposing phenotypes in mice with Smith-Magenis deletion and Potocki-Lupski duplication syndromes suggest gene dosage effects on fluid consumption behaviorDetlef H Heck, Wenli Gu, Ying Cao, et al.
Cell Reports|June 28, 2016
Notch Signaling Rescues Loss of Satellite Cells Lacking Pax7 and Promotes Brown Adipogenic DifferentiationAlessandra Pasut, Natasha C Chang, Uxia Gurriaran-Rodriguez, et al.
American Journal of Medical Genetics. Part A|April 23, 2017
Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feetMelanie Lacaria, Myriam Srour, Jacques L Michaud, et al.
Pageof 2