L. Patiño

发表

BMP15 Mutations Associated With Primary Ovarian Insufficiency Reduce Expression, Activity, or Synergy With GDF9

T. Mueller, P. Laissue, R. Gilchrist, 2017, The Journal of clinical endocrinology and metabolism.

ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure

Jacques Young, P. Laissue, N. Binart, 2018, Genetics in Medicine.

Identification of the Plasmodium falciparum rhoptry neck protein 5 (PfRON5).

H. Curtidor, M. Patarroyo, M. Patarroyo, 2011, Gene.

Plasmodium falciparum rhoptry neck protein 5 peptides bind to human red blood cells and inhibit parasite invasion

H. Curtidor, M. Vanegas, M. Patarroyo, 2014, Peptides.

PvRON2, a new Plasmodium vivax rhoptry neck antigen

H. Curtidor, M. Patarroyo, Gabriela Arévalo-Pinzón, 2011, Malaria Journal.

Binding activity, structure, and immunogenicity of synthetic peptides derived from Plasmodium falciparum CelTOS and TRSP proteins

H. Curtidor, A. Bermúdez, M. Vanegas, 2012, Amino Acids.

BMPR1A and BMPR1B missense mutations cause primary ovarian insufficiency.

Jacques Young, P. Laissue, N. Binart, 2019, The Journal of clinical endocrinology and metabolism.

Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations.

P. Laissue, H. Mateus, O. Ortega-Recalde, 2015, Fertility and sterility.

A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency

R. Veitia, P. Laissue, H. Mateus, 2017, Human molecular genetics.

Functional evidence implicating NOTCH2 missense mutations in primary ovarian insufficiency etiology

Jacques Young, P. Laissue, N. Binart, 2018, Human mutation.

New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing

Jacques Young, P. Laissue, N. Binart, 2017, Human reproduction.

Newmutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing

Jacques Young, P. Laissue, N. Binart, 2017 .

BMP15 c.-9C>G promoter sequence variant may contribute to the cause of non-syndromic premature ovarian failure.

P. Laissue, O. Ortega-Recalde, C. Restrepo, 2014, Reproductive biomedicine online.

A novel familial case of diffuse leukodystrophy related to NDUFV1 compound heterozygous mutations.

P. Laissue, M. S. van der Knaap, H. Mateus, 2013, Mitochondrion.

Exome Sequencing Is an Efficient Tool for Variant Late-Infantile Neuronal Ceroid Lipofuscinosis Molecular Diagnosis

P. Laissue, O. Ortega-Recalde, R. Battu, 2014, PloS one.

A novel mutation in KHDRBS1 in a patient affected by primary ovarian insufficiency

Jacques Young, P. Laissue, N. Binart, 2018, Clinical endocrinology.

A potential functional association between mutant BMPR2 and primary ovarian insufficiency

P. Laissue, D. Silgado, L. Patiño, 2017, Systems biology in reproductive medicine.

Binding activity, structure, and immunogenicity of synthetic peptides derived from Plasmodium falciparum CelTOS and TRSP proteins

H. Curtidor, A. Bermúdez, M. Vanegas, 2011, Amino Acids.