Boston Children's Hospital

Hospital


Location: Boston, MA, United States (USA) (US) US

ISNI: 0000000403788438

ROR: https://ror.org/00dvg7y05

Show on Map:


close-button

Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children (2019) Vivante A, Chacham OS, Shril S, Schreiber R, Mane SM, Pode-Shakked B, Soliman NA, et al. Journal article Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract (2018) Van Der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, et al. Journal article Whole exome sequencing of patients with steroid-resistant nephrotic syndrome (2018) Warejko JK, Tan W, Daga A, Schapiro D, Lawson JA, Shril S, Lovric S, et al. Journal article Comprehensive Molecular Characterization of the Hippo Signaling Pathway in Cancer. (2018) Wang Y, Xu X, Maglic D, Dill MT, Mojumdar K, Ng PKS, Jeong KJ, et al. Journal article A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity (2018) Beziat V, Li J, Lin JX, Ma CS, Li P, Bousfiha A, Pellier I, et al. Journal article CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2018) Blok LS, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, et al. Journal article Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila (2018) Straub J, Konrad E, Grüner J, Toutain A, Bok LA, Cho MT, Crawford HP, et al. Journal article Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephaly (2017) Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, et al. Journal article Genome editing using FACS enrichment of nuclease-expressing cells and indel detection by amplicon analysis (2017) Lonowski LA, Narimatsu Y, Riaz A, Delay CE, Yang Z, Niola F, Duda K, et al. Journal article Hepatic FcRn regulates albumin homeostasis and susceptibility to liver injury (2017) Pyzik M, Rath T, Kuo TT, Win S, Baker K, Hubbard JJ, Grenha R, et al. Journal article
1 ... 5 6 7 8 9