I. Vasiljeva

发表

Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia

Z. Krūmiņa, L. Gailīte, B. Lāce, 2022, Neurology: Genetics.

A novel EDA variant causing X-linked hypohidrotic ectodermal dysplasia: Case report

L. Gailīte, L. Nikitina-Zake, B. Alksere, 2021, Molecular genetics and metabolism reports.

Mutation analysis of the MSX 1 gene exons and intron in patients with nonsyndromic cleft lip and palate

A. Krūmiņa, B. Lāce, I. Akota, 2006 .

Mutation analysis of the MSX1 gene exons and intron in patients with nonsyndromic cleft lip and palate.

A. Krūmiņa, B. Lāce, I. Akota, 2006, Stomatologija.

Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies

V. Kučinskas, A. Krūmiņa, A. Utkus, 2016, BMC Musculoskeletal Disorders.

RNA Phage Qβ Coat Protein as a Carrier for Foreign Epitopes

P. Pumpens, A. Kazaks, V. Ose, 1996 .

Mosaic Qβ coats as a new presentation model

P. Pumpens, A. Kazaks, T. Kozlovska, 1998 .

Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy

B. Lāce, I. Inashkina, I. Micule, 2013, Case reports in neurological medicine.

RNA phage Q beta coat protein as a carrier for foreign epitopes.

P. Pumpens, A. Kazaks, V. Ose, 1996, Intervirology.

Mosaic Qbeta coats as a new presentation model.

P. Pumpens, A. Kazaks, V. Ose, 1998, FEBS letters.

Display vectors. II. Recombinant capsid of RNA bacteriophage Qbeta as a display moiety

P. Pumpens, A. Kazaks, V. Ose, 1997 .