J. P. Méndez

发表

Changes in the biological:immunological ratio of basal and GnRH-releasable FSH during the follicular, pre-ovulatory and luteal phases of the human menstrual cycle.

A. Olivares, A. Ulloa-Aguirre, T. Zariñán, 2001, Human reproduction.

More in-vitro bioactive, shorter-lived human chorionic gonadotrophin charge isoforms increase at the end of the first and during the third trimesters of gestation.

L. Díaz-Cueto, C. Timossi, A. Ulloa-Aguirre, 1996, Molecular human reproduction.

Amplitude regulation of episodic release, in vitro biological to immunological ratio, and median charge of human chorionic gonadotropin in pregnancy.

J. Y. Lee, L. Díaz-Cueto, J. Veldhuis, 1994, The Journal of clinical endocrinology and metabolism.

No evidence of mutations in the P450 aromatase gene in patients with polycystic ovary syndrome.

P. Canto, S. Carranza-Lira, D. Söderlund, 2005, Human reproduction.

Basal and gonadotropin-releasing hormone-releasable serum follicle-stimulating hormone charge isoform distribution and in vitro biological-to-immunological ratio in male puberty

A. Olivares, A. Ulloa-Aguirre, T. Zariñán, 2004, Endocrine.

A preponderance of circulating basic isoforms is associated with decreased plasma half-life and biological to immunological ratio of gonadotropin-releasing hormone-releasable luteinizing hormone in obese men.

J. Veldhuis, A. Olivares, A. Ulloa-Aguirre, 2000, The Journal of clinical endocrinology and metabolism.

Dynamics of basal and gonadotropin-releasing hormone-releasable serum follicle-stimulating hormone charge isoform distribution throughout the human menstrual cycle.

L. Díaz-Cueto, J. Veldhuis, A. Olivares, 1995, The Journal of clinical endocrinology and metabolism.

Bone mineral density in postmenopausal Mexican-Mestizo women with normal body mass index, overweight, or obesity

R. Coral-Vázquez, D. Rojano-Mejía, A. Coronel, 2012, Menopause.

Mutations in the desert hedgehog (DHH) gene in patients with 46,XY complete pure gonadal dysgenesis.

P. Canto, D. Söderlund, J. P. Méndez, 2004, The Journal of clinical endocrinology and metabolism.

Increased FNDC5/IRISIN protein expression in breast cancer tissue is associated with obesity in postmenopausal women

V. Bautista-Piña, R. Coral-Vázquez, P. Canto, 2021, Journal of Clinical Pathology.

Different body mass indexes and their relation to prognosis of early-stage breast cancer in postmenopausal Mexican-Mestizo women

P. Canto, J. P. Méndez, A. Morales, 2020, Women & health.

In vitro and molecular modeling analysis of two mutant desert hedgehog proteins associated with 46,XY gonadal dysgenesis.

M. Soriano-Ursúa, R. Coral-Vázquez, P. Canto, 2013, DNA and cell biology.

PPARGC1A and ADIPOQ polymorphisms are associated with aggressive prostate cancer in Mexican-Mestizo men with overweight or obesity.

R. Coral-Vázquez, D. Rojano-Mejía, P. Canto, 2017, Cancer biomarkers : section A of Disease markers.

DNA binding activity studies and computational approach of mutant SRY in patients with 46, XY complete pure gonadal dysgenesis

P. Canto, B. Cisneros, J. P. Méndez, 2009, Molecular and Cellular Endocrinology.

Complete sequence of the ATP6 and ND3 mitochondrial genes in breast cancer tissue of postmenopausal women with different body mass indexes.

R. Coral-Vázquez, P. Canto, J. P. Méndez, 2018, Annals of diagnostic pathology.

Genetic variants in ATP6 and ND3 mitochondrial genes are not associated with aggressive prostate cancer in Mexican–Mestizo men with overweight or obesity

D. Rojano-Mejía, P. Canto, J. P. Méndez, 2016, The aging male : the official journal of the International Society for the Study of the Aging Male.

Bone mineral density in postmenopausal Mexican-Mestizo women with normal body mass index, overweight, or obesity.

R. Coral-Vázquez, D. Rojano-Mejía, A. Coronel, 2013, Menopause.

Polymorphic changes in the KAL1 gene: Not all of them should be classified as polymorphisms

D. Söderlund, J. P. Méndez, F. Vilchis, 2004, Journal of endocrinological investigation.

The gonadal expression pattern of lipocalin-2 and 24p3 receptor is modified in the gonads of the offspring of obese rats

J. P. Méndez, M. C. Revilla-Monsalve, L. Manuel-Apolinar, 2020, Molecular medicine reports.

(−)‐Epicatechin improves body composition of male rats descendant of obese mothers postnatally fed with a high‐fat diet

R. Coral-Vázquez, M. Menjivar, P. Canto, 2022, Fundamental & clinical pharmacology.

(−)-Epicatechin modifies body composition of the male offspring of obese rats

R. Coral-Vázquez, M. Menjivar, P. Canto, 2019, Journal of Functional Foods.

Molecular analysis of the 5 alpha-steroid reductase type 2 gene in a family with deficiency of the enzyme.

P. Canto, A. Ulloa-Aguirre, J. P. Méndez, 1997, American journal of medical genetics.

Inherited impairment of nuclear androgen uptake as a cause of familial androgen insensitivity

A. Ulloa-Aguirre, J. P. Méndez, G. Pérez-palacios, 1988 .

The syndromes of androgen resistance revisited.

A. Ulloa-Aguirre, J. P. Méndez, J. McGinley, 1987, Journal of steroid biochemistry.

A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome.

J. Zenteno, A. Ulloa-Aguirre, J. P. Méndez, 1998, The Journal of clinical endocrinology and metabolism.

Self-priming effect of luteinizing hormone-human chorionic gonadotropin (hCG) upon the biphasic testicular response to exogenous hCG. I. Serum testosterone profile.

A. Ulloa-Aguirre, J. P. Méndez, G. Pérez-palacios, 1985, The Journal of clinical endocrinology and metabolism.

Mutation analysis of the WNT-4 gene in patients with polycystic ovary syndrome

P. Canto, S. Carranza-Lira, D. Söderlund, 2006, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome

F. Larrea, A. Ulloa-Aguirre, J. P. Méndez, 2001, Journal of Human Genetics.

Incomplete regression of müllerian ducts in the androgen insensitivity syndrome.

S. Carranza-Lira, A. Ulloa-Aguirre, J. P. Méndez, 1990, Fertility and sterility.

Changes in the responsiveness of prolactin secretion to dopaminergic blockade and TRH stimulation throughout sexual maturation in men

J. Garza-flores, A. Ulloa-Aguirre, J. P. Méndez, 1990, Psychoneuroendocrinology.

Molecular analysis of the SRD5A2 in 46,XY subjects with incomplete virilization: the P212R substitution of the steroid 5alpha-reductase 2 may constitute an ancestral founder mutation in Mexican patients.

P. Canto, J. P. Méndez, B. Chávez, 2010, Journal of andrology.

Codon 89 polymorphism of the human 5α‐steroid reductase type 2 gene

P. Canto, D. Hernández, J. P. Méndez, 1997 .

A heterozygous mutation in the desert hedgehog gene in patients with mixed gonadal dysgenesis.

P. Canto, D. Söderlund, J. P. Méndez, 2005, Molecular human reproduction.

Mutational analysis of the luteinizing hormone receptor gene in two individuals with Leydig cell tumors.

P. Canto, D. Söderlund, J. P. Méndez, 2002, American journal of medical genetics.

Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.

P. Canto, D. Söderlund, J. P. Méndez, 2008, Journal of andrology.

Experience of an eating disorders out-patient program in an internal medicine hospital

J. P. Méndez, M. Kaufer-Horwitz, V. Vázquez-Velázquez, 2013, Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity.

Endocrine evaluation in a patient with MURCS association and ovarian agenesis.

O. Mutchinick, A. Ulloa-Aguirre, J. P. Méndez, 1986, European journal of obstetrics, gynecology, and reproductive biology.

Screening for mutations in the SRY gene in patients with mixed gonadal dysgenesis or with Turner syndrome and Y mosaicism.

P. Canto, D. Söderlund, J. P. Méndez, 2004, European journal of obstetrics, gynecology, and reproductive biology.

Ascertainment and mutational studies of SRY in nine XY females.

R. Erickson, P. Graves, J. P. Méndez, 1999, American journal of medical genetics.

Mutations of the 5 alpha-reductase type 2 gene in eight Mexican patients from six different pedigrees with 5 alpha-reductase-2 deficiency.

J. Imperato-McGinley, P. Canto, O. Mutchinick, 1997, Clinical endocrinology.

Duplication of SOX9 associated with 46,XX ovotesticular disorder of sex development.

R. Coral-Vázquez, P. Canto, R. Calzada-León, 2018, Reproductive biomedicine online.

Hyperprolactinemia inhibits natural killer (NK) cell functionin vivo and its bromocriptine treatment not only corrects it but makes it more efficient

D. Alarcón-Segovia, F. Larrea, A. Villa, 1992, Journal of Clinical Immunology.

Regulation of follicle-stimulating and luteinizing hormone receptor signaling by “regulator of G protein signaling” proteins

J. P. Méndez, C. Castro-Fernández, G. Maya-Núñez, 2004, Endocrine.

Molecular basis of hypogonadotropic hypogonadism: restoration of mutant (E(90)K) GnRH receptor function by a deletion at a distant site.

P. Conn, J. Janovick, A. Ulloa-Aguirre, 2002, The Journal of clinical endocrinology and metabolism.

A novel homozygous mutation in the second transmembrane domain of the gonadotrophin releasing hormone receptor gene

P. Canto, A. Ulloa-Aguirre, D. Söderlund, 2001, Clinical endocrinology.

T-cell dysregulation in patients with hyperprolactinemia: effect of bromocriptine treatment.

D. Alarcón-Segovia, J. Alcocer-Varela, F. Larrea, 1986, Clinical immunology and immunopathology.

Expression profiling of lipocalin-2 and 24p3 receptor in murine gonads at different developmental stages

A. Olivares, J. P. Méndez, L. Manuel-Apolinar, 2018, Experimental and therapeutic medicine.

Is there any physiological role for gonadotrophin oligosaccharide heterogeneity in humans? I. Gondatrophins are synthesized and released in multiple molecular forms. A matter of fact.

C. Timossi, A. Ulloa-Aguirre, J. P. Méndez, 2001, Human reproduction.

Clinical expression and SRY gene analysis in XY subjects lacking gonadal tissue.

P. Canto, J. Zenteno, J. P. Méndez, 2001, American journal of medical genetics.

Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.

P. Canto, J. Zenteno, D. Söderlund, 2004, Cancer genetics and cytogenetics.

Frequency of Y chromosomal material in Mexican patients with Ullrich-Turner syndrome.

P. Canto, J. P. Méndez, A. Cervantes, 1998, American journal of medical genetics.

A mutation in the 5' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism.

P. Canto, A. Ulloa-Aguirre, J. P. Méndez, 2000, The Journal of clinical endocrinology and metabolism.

Two SRY-negative XX male brothers without genital ambiguity

J. Zenteno, J. P. Méndez, Marisol López, 1997, Human Genetics.

Clinical traits and molecular findings in 46,XX males

R. Erickson, J. P. Méndez, Marisol López, 1995, Clinical genetics.

Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypes.

R. Erickson, P. Canto, J. P. Méndez, 1996, American journal of medical genetics.

A reliable endocrine test with human menopausal gonadotropins for diagnosis of true hermaphroditism in early infancy.

L. Díaz-Cueto, P. Canto, A. Ulloa-Aguirre, 1998, The Journal of clinical endocrinology and metabolism.

The presence of Müllerian remnants in the complete androgen insensitivity syndrome: a steroid hormone-mediated defect?

A. Ulloa-Aguirre, J. P. Méndez, G. Pérez-palacios, 1986, Fertility and sterility.

Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA.

P. Canto, J. Zenteno, J. P. Méndez, 2000, American journal of medical genetics.

Mixed gonadal dysgenesis: clinical, cytogenetic, endocrinological, and histopathological findings in 16 patients.

O. Mutchinick, A. Ulloa-Aguirre, J. P. Méndez, 1993, American journal of medical genetics.

Male pseudohermaphroditism due to primary 5α-reductase deficiency: Variation in gender identity reversal in seven Mexican patients from five different pedigrees

J. Imperato-McGinley, C. Shackleton, A. Ulloa-Aguirre, 1995, Journal of endocrinological investigation.

Reproductive axis function and gonadotropin microheterogeneity in a male rat model of diet-induced obesity.

E. Zambrano, A. Tovar, A. Olivares, 2010, General and comparative endocrinology.

Studies on the microheterogeneity of chorionic gonadotrophin secreted by the human cytotrophoblast in culture.

A. Cravioto, A. Ulloa-Aguirre, J. P. Méndez, 1990, Human reproduction.

Pituitary-testicular axis function, biological to immunological ratio and charge isoform distribution of pituitary LH in male rats with experimental diabetes.

A. Olivares, G. Perera-Marín, A. Ulloa-Aguirre, 2009, General and comparative endocrinology.

In vitro biological-to-immunological ratio of serum gonadotropins throughout male puberty in children with insulin-dependent diabetes mellitus

A. Ulloa-Aguirre, D. Söderlund, J. P. Méndez, 2007, Endocrine.

No evidence of mutations in the follicle-stimulating hormone receptor gene in Mexican women with 46,XX pure gonadal dysgenesis.

P. Canto, A. Ulloa-Aguirre, J. P. Méndez, 2001, American journal of medical genetics.

Identification of three novel mutations in the KAL1 gene in patients with Kallmann syndrome.

P. Canto, D. Söderlund, J. P. Méndez, 2002, The Journal of clinical endocrinology and metabolism.

On the nature of the follicle-stimulating signal delivered to the ovary during exogenously controlled follicular maturation. A search into the immunological and biological attributes and the molecular composition of two preparations of urofollitropin.

L. Díaz-Cueto, A. Olivares, C. Timossi, 1995, Archives of medical research.

Studies on gonadal dysgenesis: variable expressivity of the XY testicular dysgenesis syndrome; two case reports.

A. Ulloa-Aguirre, J. P. Méndez, G. Pérez-palacios, 1989, European journal of obstetrics, gynecology, and reproductive biology.

Endocrine and biochemical studies in a 46,XY phenotypically male infant with 17-ketosteroid reductase deficiency.

O. Mutchinick, S. Bassol, A. Ulloa-Aguirre, 1985, The Journal of clinical endocrinology and metabolism.

Fbxw15/Fbxo12J Is an F-Box Protein-Encoding Gene Selectively Expressed in Oocytes of the Mouse Ovary1

S. Ojeda, J. P. Méndez, B. Kerr, 2008, Biology of reproduction.

Sera from women with different metabolic and menopause states differentially regulate cell viability and Akt activation in a breast cancer in-vitro model

F. Vadillo-Ortega, J. L. Ventura-Gallegos, S. Pedraza-Sánchez, 2022, PloS one.

FBXW 12 , a novel F box protein-encoding gene , is deleted or methylated in some cases of epithelial ovarian cancer

S. Ojeda, R. López-Romero, M. Salcedo, 2015 .

Low Serum Testosterone/Dihydrotestosterone Patients Ratio in with Pancreatic Carcinoma

E. Wolpert, J. P. Méndez, G. Robles-Díaz, 1987 .

Evidence for genetic heterogeneity in male pseudohermaphroditism due to Leydig cell hypoplasia.

P. Canto, J. Zenteno, J. P. Méndez, 1999, The Journal of clinical endocrinology and metabolism.

Impact of genetic variants of IL-6, IL6R, LRP5, ESR1 and SP7 genes on bone mineral density in postmenopausal Mexican-Mestizo women with obesity.

R. Coral-Vázquez, D. Rojano-Mejía, P. Canto, 2013, Gene.

Screening for mutations in the WNT-4 gene in patients with 46,XX true hermaphroditism.

P. Canto, R. Calzada-León, D. Söderlund, 2004, Molecular genetics and metabolism.

Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population

M. Tusié-Luna, J. Cabello-Villegas, R. Calzada-León, 1996, Human Genetics.

A new inherited variant of the 3 beta-hydroxysteroid dehydrogenase-isomerase deficiency syndrome: evidence for the existence of two isoenzymes.

A. Ulloa-Aguirre, J. P. Méndez, R. Lisker, 1986, The Journal of clinical endocrinology and metabolism.

Overweight and obesity in men with prostate cancer do not constitute risk factors for biochemical recurrence

P. Canto, J. P. Méndez, G. Feria-Bernal, 2020, The aging male : the official journal of the International Society for the Study of the Aging Male.

Scant XYqh- testicular cells with normal SRY was enough to differentiate bilateral testes in a 45,X/46,XYqh- patient.

P. Canto, A. Ulloa-Aguirre, J. P. Méndez, 1999, European journal of obstetrics, gynecology, and reproductive biology.

Association of a TFAM haplotype with aggressive prostate cancer in overweight or obese Mexican Mestizo men.

D. Rojano-Mejía, P. Canto, J. P. Méndez, 2017, Urologic oncology.

Full-length SRY protein is essential for DNA binding.

R. Coral-Vázquez, P. Canto, J. P. Méndez, 2008, Molecular human reproduction.

Low serum testosterone/dihydrotestosterone ratio in patients with pancreatic carcinoma.

E. Wolpert, J. P. Méndez, G. Robles-Díaz, 1987, Pancreas.

(-)-Epicatechin reduces adiposity in male offspring of obese rats

R. Coral-Vázquez, P. Canto, L. Reyes-Castro, 2019, Journal of Developmental Origins of Health and Disease.

SRY alone can induce normal male sexual differentiation.

R. Erickson, J. P. Méndez, G. Pérez-palacios, 1995, American journal of medical genetics.

Expression of adipokines and their receptors in adipose tissue of women with class 3 obesity with or without hypertension.

R. Coral-Vázquez, P. Canto, J. P. Méndez, 2019, Gene.

Serum concentrations of apelin-17 isoform vary in accordance to blood pressure categories in individuals with obesity class 3

P. Canto, J. P. Méndez, Silvia Trejo, 2019, Clinical and experimental hypertension.

Extreme androgen resistance in a kindred with a novel insertion/deletion mutation in exon 5 of the androgen receptor gene

J. Zenteno, J. P. Méndez, S. Kofman‐Alfaro, 2003, Journal of Human Genetics.

Adiponectin and adiponectin receptor 1 expression proteins levels are modified in breast cancer in postmenopausal women with obesity

V. Bautista-Piña, R. Coral-Vázquez, P. Canto, 2020, Journal of Clinical Pathology.

Leptin and its receptor are overexpressed in breast cancer tissue of postmenopausal Mexican-Mestizo women with obesity.

V. Bautista-Piña, R. Coral-Vázquez, P. Canto, 2021, Annals of diagnostic pathology.

Codon 89 polymorphism of the human 5alpha-steroid reductase type 2 gene.

P. Canto, D. Hernández, J. P. Méndez, 1997, Clinical genetics.

Eating behavior and psychological profile: associations between daughters with distinct eating disorders and their mothers

Lucy María Reidl-Martínez, J. P. Méndez, M. Kaufer-Horwitz, 2017, BMC Women's Health.

(-)-EPICATECHIN INCREASES APELIN/APLNR EXPRESSION AND MODIFIES PROTEINS INVOLVED IN LIPID METABOLISM OF OFFSPRING DESCENDANTS OF MATERNAL OBESITY.

R. Coral-Vázquez, P. Canto, L. Reyes-Castro, 2023, The Journal of nutritional biochemistry.

High Knowledge About Obesity and its Health Risks, with the Exception of Cancer, Among Mexican Individuals

J. P. Méndez, E. García‐García, S. Ponce de León Rosales, 2012, Journal of Cancer Education.

The R137W Adrenocorticotropin Receptor Gene Mutation: A Mutational Hot Spot?

D. Söderlund, J. P. Méndez, E. Nishimura, 2005 .

WHOLE SEQUENCING OF THE MITOCHONDRIAL GENOME OF BREAST CANCER TISSUE IN MEXICAN-MESTIZO POSTMENOPAUSAL WOMEN WITH DIFFERENT BODY MASS INDEX.

R. Coral-Vázquez, P. Canto, J. Zenteno, 2019, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion.

Knowledge of appropriate foods and beverages needed for weight loss and diet of patients in an Obesity Clinic

J. P. Méndez, M. Kaufer-Horwitz, J. Domínguez-García, 2014, European Journal of Clinical Nutrition.

A novel mutation of the insulin-like 3 gene in patients with cryptorchidism

P. Canto, S. Carranza-Lira, D. Söderlund, 2003, Journal of Human Genetics.

Complete sequence of the ANKK1 gene in Mexican-Mestizo individuals with obesity, with or without binge eating disorder

D. Rojano-Mejía, P. Canto, J. P. Méndez, 2018, European Psychiatry.