E. Esquivel

发表

Podocin inactivation in mature kidneys causes focal segmental glomerulosclerosis and nephrotic syndrome.

M. Dallman, G. Mollet, C. Antignac, 2009, Journal of the American Society of Nephrology : JASN.

Biliary and pancreatic dysgenesis in mice harboring a mutation in Pkhd1.

D. Jain, S. Somlo, L. Onuchic, 2008, The American journal of pathology.

Increased lysosomal proteolysis counteracts protein accumulation in the proximal tubule during focal segmental glomerulosclerosis.

G. Mollet, C. Antignac, E. Christensen, 2013, Kidney international.

Idiopathic Nephrotic Syndrome

C. Antignac, E. Esquivel, Ernie L. Esquivel, 2009 .

Lessons Learned by Medical Students about Systems-Based Practice as Patients Transition their Care

S. Katz, D. Jannat-Khah, L. Greisman, 2021 .

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

O. Gribouval, C. Antignac, P. Niaudet, 2004, Kidney international.

A missense mutation in podocin leads to early and severe renal disease in mice.

C. Antignac, C. Antignac, M. Gubler, 2008, Kidney international.

Impact of diagnostic bone biopsies on the management of non-vertebral osteomyelitis

D. Jannat-Khah, O. Vielemeyer, S. Kapadia, 2019, Medicine.

Idiopathic Nephrotic Syndrome: Genetic Aspects

C. Antignac, E. Machuca, E. Esquivel, 2009 .

Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome.

T. Benzing, O. Gribouval, C. Antignac, 2008, Journal of the American Society of Nephrology : JASN.

PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats.

E. Avner, Z. Ren, K. Zerres, 2002, American journal of human genetics.

Kidney: Hereditary Disorders

S. Somlo, E. Esquivel, 2006 .

Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutations.

Carsten Bergmann, Klaus Zerres, Ali Gharavi, 2003, Journal of the American Society of Nephrology : JASN.

Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene.

E. Avner, Z. Ren, K. Zerres, 2002, Journal of the American Society of Nephrology : JASN.

Maternal environment interacts with modifier genes to influence progression of nephrotic syndrome.

M. Kretzler, G. Mollet, C. Antignac, 2008, Journal of the American Society of Nephrology : JASN.

Transitioning preclinical students into clerkships amidst curricular disruptions from the COVID-19 pandemic

Erika L. Abramson, J. Safdieh, E. Abramson, 2021, Medical education online.

AAIM Recommendations for the 2020-2021 Internal Medicine Residency Application Cycle in Response to the COVID-19 Pandemic

Katherine C. Chretien, L. Willett, S. Chheda, 2020, The American Journal of Medicine.

Podocin inactivation in mature kidneys causes focal segmental glomerulosclerosis and nephrotic syndrome.

M. Dallman, G. Mollet, C. Antignac, 2009, Journal of the American Society of Nephrology : JASN.