Detalhe da pesquisa
1.
AQP5 enriches for stem cells and cancer origins in the distal stomach.
Nature
; 578(7795): 437-443, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32025032
2.
Enzyme replacement therapy desensitization in a child with infantile onset Pompe disease.
Asian Pac J Allergy Immunol
; 40(4): 414-417, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32061243
3.
Turner syndrome in diverse populations.
Am J Med Genet A
; 182(2): 303-313, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31854143
4.
To B(enign) or Not to B: functionalisation of variant in a mild form of argininosuccinate lyase deficiency identified through newborn screening.
Clin Dysmorphol
; 33(1): 43-49, 2024 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37865865
5.
Evaluating treatment options for cardiovascular autonomic neuropathy in patients with diabetes mellitus: a systematic review.
Diabetol Int
; 14(3): 224-242, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37397902
6.
An ex vivo platform to guide drug combination treatment in relapsed/refractory lymphoma.
Sci Transl Med
; 14(667): eabn7824, 2022 10 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36260690
7.
A constant pool of Lgr5+ intestinal stem cells is required for intestinal homeostasis.
Cell Rep
; 34(4): 108633, 2021 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33503423
8.
An Investigation of Sensory Specific Satiety and Food Size When Children Consume a Whole or Diced Vegetable.
Foods
; 6(7)2017 Jul 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-28737712
9.
Lgr5-expressing chief cells drive epithelial regeneration and cancer in the oxyntic stomach.
Nat Cell Biol
; 19(7): 774-786, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28581476
10.
Whole-genome sequencing reveals potent therapeutic strategy for monomorphic epitheliotropic intestinal T-cell lymphoma.
Blood Adv
; 4(19): 4769-4774, 2020 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33017466
11.
Application of an ex-vivo drug sensitivity platform towards achieving complete remission in a refractory T-cell lymphoma.
Blood Cancer J
; 10(1): 9, 2020 01 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31988286
12.
TFAP2A mutation in a child and mother with predominantly ocular anomalies: non-classical presentation of branchio-oculo-facial syndrome.
Clin Dysmorphol
; 28(4): 215-218, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31490282