P. Barros-Núñez

发表

Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia.

S. Cichon, M. Nöthen, A. Hillmer, 1999, The Journal of investigative dermatology.

CD44 Genotypes Are Associated with Susceptibility and Tumor Characteristics in Colorectal Cancer Patients.

S. Flores-Martínez, J. Śanchez-Corona, P. Barros-Núñez, 2020, The Tohoku journal of experimental medicine.

A de novo t(10;19)(q22.3;q13.33) leads to ZMIZ1/PRR12 reciprocal fusion transcripts in a girl with intellectual disability and neuropsychiatric alterations

A. Rivas-Estilla, R. Ortíz-López, P. Barros-Núñez, 2015, neurogenetics.

Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene.

P. Barros-Núñez, J M Mantilla-Capacho, L Arnaud, 2005, Genetic counseling.

Hamartoma Involving the Pseudarthrosis Site in Patients With Neurofibromatosis Type 1

P. Barros-Núñez, A. González-mendoza, R. Mariaud-Schmidt, 2005, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Gene expression profiling demonstrates WNT/β-catenin pathway genes alteration in Mexican patients with colorectal cancer and diabetes mellitus.

J. Śanchez-Corona, P. Barros-Núñez, Laura Ivonne Wence-Chavez, 2017, Journal of B.U.ON. : official journal of the Balkan Union of Oncology.

Genotypes and Haplotypes in the AXIN2 and TCF7L2 Genes are Associated With Susceptibility and With Clinicopathological Characteristics in Breast Cancer Patients

S. Flores-Martínez, J. Śanchez-Corona, P. Barros-Núñez, 2022, British Journal of Biomedical Science.

[WNT-β-catenin signaling pathway and its relationship with cancer].

P. Barros-Núñez, M. A. Rosales-Reynoso, C. Juárez-Vázquez, 2012, Cirugia y cirujanos.

True vs. false inv(Y)(p11q11.2): a familial instance concurrent with trisomy 21.

P. Barros-Núñez, H. Rivera, M. Gutiérrez-Angulo, 2002, Annales de genetique.

Title MHC class I-related chain A and B ligands are differentially expressed in human cervical cancer cell lines

A. Aguilar-Lemarroy, L. Jave-Suárez, P. Barros-Núñez, 2011 .

A. Aguilar-Lemarroy, L. Jave-Suárez, P. Barros-Núñez, 2011, Cancer Cell International.

Detection of monoclonal IGH rearrangements in circulating cells from healthy first-degree relatives of patients with multiple myeloma

P. Barros-Núñez, Esperanza Barrera-Chairez, V. Rosales-García, 2014, Medical Oncology.

Diastrophic dysplasia and atelosteogenesis type II as expression of compound heterozygosis: First report of a Mexican patient and genotype–phenotype correlation

A. Mégarbané, P. Barros-Núñez, N. Macías-Gómez, 2004, American journal of medical genetics. Part A.

XRCC1 polymorphisms and haplotypes in Mexican patients with acute lymphoblastic leukemia.

J. P. Meza-Espinoza, P. Barros-Núñez, M. Gutiérrez-Angulo, 2009, Genetics and molecular research : GMR.

46,XX ovotesticular disorder in a Mexican patient with Beckwith–Wiedemann syndrome: a case report

P. Barros-Núñez, H. Rivera, M. Gutiérrez-Angulo, 2012, Journal of Medical Case Reports.

Clinical and genetic heterogeneity in patients with mosaic variegated aneuploidy: Delineation of clinical subtypes

P. Barros-Núñez, H. Rivera, H. García-Castillo, 2008, American journal of medical genetics. Part A.

Micronutrient content and antioxidant enzyme activities in human breast milk.

T. Zenteno-Savín, L. Méndez-Rodríguez, P. Barros-Núñez, 2019, Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements.

Genetic Polymorphisms in APC, DVL2, and AXIN1 Are Associated with Susceptibility, Advanced TNM Stage or Tumor Location in Colorectal Cancer.

S. Flores-Martínez, J. Śanchez-Corona, P. Barros-Núñez, 2019, The Tohoku journal of experimental medicine.

FMR1 protein expression in blood smears for fragile X syndrome diagnosis in a Mexican population sample.

R. Willemsen, P. Barros-Núñez, M. A. Rosales-Reynoso, 2010, Genetic testing and molecular biomarkers.

Detection of clonal immunoglobulin and T-cell receptor gene recombination in hematological malignancies: monitoring minimal residual disease.

P. Barros-Núñez, H. García-Castillo, 2009, Cardiovascular & hematological disorders drug targets.

TCF7L2 and CCND1 polymorphisms and its association with colorectal cancer in Mexican patients.

S. Flores-Martínez, J. Śanchez-Corona, P. Barros-Núñez, 2016, Cellular and molecular biology.

Evolution and genomics of the human brain

P. Barros-Núñez, M. A. Rosales-Reynoso, C. Juárez-Vázquez, 2018 .

Mutations in CEP57 cause mosaic variegated aneuploidy syndrome

N. Rahman, D. Gisselsson, J. Clayton-Smith, 2011, Nature Genetics.

Protective role of +294 T/C (rs2016520) polymorphism of PPARD in Mexican patients with colorectal cancer.

S. Flores-Martínez, J. Śanchez-Corona, P. Barros-Núñez, 2017, Genetics and molecular research : GMR.

Familial whole-arm translocations (1;19), (9;13), and (12;21): a review of 101 constitutional exchanges

M. Rocchi, P. Barros-Núñez, H. Rivera, 2010, Journal of Applied Genetics.

Detection and monitoring of clonality in peripheral blood and bone marrow of patients with B‐cell lymphoproliferative disorders

P. Barros-Núñez, E. Leal, B. López-Guido, 2003, Hematological oncology.

Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval

J. Weissenbach, P. Beighton, M. Hamida, 1996, Human Genetics.

MKK4 variants rs3826392 and rs3809728 are associated with susceptibility and clinicopathological features in colorectal cancer patients

S. Flores-Martínez, P. Barros-Núñez, A. M. Saucedo-Sariñana, 2021, Iranian Journal of Basic Medical Sciences.

De novo dir dup (1)(q3200----4200) in an adult. Further delineation of the pure 1q trisomy syndrome.

J. Śanchez-Corona, P. Barros-Núñez, C. Medina, 1989, Annales de Genetique.

Two familial intrachromosomal insertions with maternal dup(6)(p22.3p25.3) or dup(2)(q24.2q32.1) in recombinant offspring

M. Partida-Pérez, A. Aguilar-Lemarroy, L. Jave-Suárez, 2017, Clinical dysmorphology.

High sensitivity of chemiluminescent methodology for detection of clonal CDR3 sequences in patients with acute lymphoblastic leukemia

P. Barros-Núñez, E. Leal, A. Jaloma-Cruz, 2004, Hematological oncology.

Crouzon with acanthosis nigricans. Further delineation of the syndrome

P. Barros-Núñez, L. Arnaud-Lopez, J. Mantilla-Capacho, 2007, Clinical genetics.

Williams–Beuren syndrome in Mexican patients confirmed by FISH and assessed by aCGH

J. García-Ortiz, A. Aguilar-Lemarroy, L. Jave-Suárez, 2019, Journal of Genetics.

Femoral-facial syndrome with malformations in the central nervous system.

P. Barros-Núñez, E. Leal, N. Macías-Gómez, 2003, Clinical imaging.

MDR1 C3435T Polymorphism in Mexican Children with Acute Lymphoblastic Leukemia and in Healthy Individuals

J. P. Meza-Espinoza, M. Partida-Pérez, P. Barros-Núñez, 2008, Human biology.

Detection of monoclonal B cells in general population from two different regions of Mexico

M. T. Magaña-Torres, P. Barros-Núñez, Sergio Yair Rodríguez-Preciado, 2017, International journal of immunogenetics.

De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome features.

R. Ortíz-López, P. Barros-Núñez, A. Rojas-Martínez, 2013, Gene.

Gene expression profiling identifies WNT7A as a possible candidate gene for decreased cancer risk in fragile X syndrome patients.

A. Aguilar-Lemarroy, L. Jave-Suárez, P. Barros-Núñez, 2010, Archives of medical research.

Genetic variation of the FMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and Tarahumara

P. Barros-Núñez, M. A. Rosales-Reynoso, B. Ibarra, 2008, American journal of human biology : the official journal of the Human Biology Council.

PCR approach for detection of Fragile X syndrome and Huntington disease based on modified DNA: limits and utility.

P. Barros-Núñez, M. A. Rosales-Reynoso, L. Sandoval, 2007, Genetic testing.

Genetic diversity at the FMR1 locus in Mexican population.

P. Barros-Núñez, M. A. Rosales-Reynoso, R. Troyo-Sanromán, 2005, Archives of medical research.

High recurrence of recombinants in a family with pericentric inversion of chromosome 18.

P. Barros-Núñez, G. Mejía-Baltodano, L. Bobadilla, 1997, Annales de genetique.

Insulin glargine affects the expression of Igf-1r, Insr, and Igf-1 genes in colon and liver of diabetic rats

S. Flores-Martínez, J. Śanchez-Corona, P. Barros-Núñez, 2018, Iranian journal of basic medical sciences.

Clinical and molecular characterization of Costello syndrome in unrelated Mexican patients

M. T. Magaña-Torres, P. Barros-Núñez, B. E. Ríos-González, 2021, Clinical dysmorphology.

Circulating cell-free-DNA concentration is a good biomarker for diagnosis of colorectal cancer in Mexican patients Cellular and Molecular Biology

P. Barros-Núñez, A. M. Saucedo-Sariñana, M. Gallegos-Arreola, 2022 .

Peripheral T-lymphocytes express WNT7A and its restoration in leukemia-derived lymphoblasts inhibits cell proliferation

A. Aguilar-Lemarroy, L. Jave-Suárez, P. Barros-Núñez, 2012, BMC Cancer.

Epigenetic mechanisms in the development of memory and their involvement in certain neurological diseases.

P. Barros-Núñez, M. A. Rosales-Reynoso, C. Juárez-Vázquez, 2016 .

Neuhauser syndrome: a rare association of megalocornea and mental retardation. Review of the literature and further phenotype delineation.

P. Barros-Núñez, B. E. Gutiérrez-Amavizca, R. Orozco-Castellanos, 2013, Genetic counseling.

Melorheostosis: unusual presentation in a girl.

P. Barros-Núñez, R. Mariaud-Schmidt, W. E. Bitar, 2002, Clinical imaging.

Variegated-like mosaicism and ring syndrome in a r(4) boy. Appraisal of 38 patients with a fairly complete ring 4.

P. Barros-Núñez, H. Rivera, I. González-Ramos, 2010, Genetic Counseling.

A de novo t(10;19)(q22.3;q13.33) leads to ZMIZ1/PRR12 reciprocal fusion transcripts in a girl with intellectual disability and neuropsychiatric alterations

A. Rivas-Estilla, R. Ortíz-López, P. Barros-Núñez, 2015, neurogenetics.

GSK 3 β Polymorphisms Are Associated with Tumor Site and TNM Stage in Colorectal Cancer

S. Flores-Martínez, J. Śanchez-Corona, P. Barros-Núñez, 2019 .

AXIN2 Polymorphisms and Their Association with Colorectal Cancer in Mexican Patients.

S. Flores-Martínez, J. Śanchez-Corona, P. Barros-Núñez, 2016, Genetic testing and molecular biomarkers.

A novel mutation in CDMP1 causes brachydactyly type C with "angel-shaped phalanx". A genotype-phenotype correlation in the mutational spectrum.

F. Escande, P. Barros-Núñez, B. E. Gutiérrez-Amavizca, 2012, European journal of medical genetics.

Williams–Beuren syndrome in Mexican patients confirmed by FISH and assessed by aCGH

J. García-Ortiz, A. Aguilar-Lemarroy, L. Jave-Suárez, 2019, Journal of Genetics.

Unexpected familial recurrence of iris coloboma. A delayed mutation mechanism?

J. Śanchez-Corona, P. Barros-Núñez, C. Medina, 1995, Clinical genetics.

Molecular characterization of the--SEA alpha thalassemia allele in Mexican patients with HbH disease.

J. Perea, P. Barros-Núñez, B. Ibarra, 2006, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion.

A. Aguilar-Lemarroy, L. Jave-Suárez, P. Barros-Núñez, 2011, Cancer Cell International.

Cardio‐facio‐cutaneous syndrome with hemihidrosis: ectodermal dysplasias spectrum?

P. Barros-Núñez, M. Gutiérrez-Angulo, N. Macías-Gómez, 2006, International journal of dermatology.

Circulating cell-free-DNA concentration is a good biomarker for diagnosis of colorectal cancer in Mexican patients.

P. Barros-Núñez, A. M. Saucedo-Sariñana, M. Gallegos-Arreola, 2022, Cellular and molecular biology.