Artykuły udostępnione publicznie: - Keith Choate MD, PhDWięcej informacji
Niedostępne w żadnym miejscu: 5
Symptomatic congenital hemangioma and congenital hemangiomatosis associated with a somatic activating mutation in GNA11
T Funk, Y Lim, AM Kulungowski, L Prok, TM Crombleholme, K Choate, ...
JAMA dermatology 152 (9), 1015-1020, 2016
Upoważnienia: Doris Duke Charitable Foundation
Hair and skin predict cardiomyopathies: Carvajal and erythrokeratodermia cardiomyopathy syndromes
Q Sun, L Wine Lee, EK Hall, KA Choate, RW Elder
Pediatric Dermatology 38 (1), 31-38, 2021
Upoważnienia: US National Institutes of Health
Somatic mutation profile of atypical fibroxanthoma and cutaneous undifferentiated pleomorphic sarcoma
YH Lim, TD Zaki, JL Levinsohn, A Galan, KA Choate, AM Hanlon
Dermatologic Surgery 47 (2), 290-292, 2021
Upoważnienia: US National Institutes of Health, Doris Duke Charitable Foundation
Nagashima‐type palmoplantar keratoderma: Case series and two novel variants
M Braun, KA Choate, EF Mathes
Pediatric Dermatology 40 (5), 882-885, 2023
Upoważnienia: US National Institutes of Health
Congenital verrucous plaques.
MA Leszczynska, K Schiele, J Cervantes, K Choate, ML Levy
Pediatric Dermatology 38 (5), 2021
Upoważnienia: US National Institutes of Health
Dostępne w jakimś miejscu: 88
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
LM Boyden, M Choi, KA Choate, CJ Nelson-Williams, A Farhi, HR Toka, ...
Nature 482 (7383), 98-102, 2012
Upoważnienia: US National Institutes of Health, Howard Hughes Medical Institute
Mitotic recombination in patients with ichthyosis causes reversion of dominant mutations in KRT10
KA Choate, Y Lu, J Zhou, M Choi, PM Elias, A Farhi, C Nelson-Williams, ...
Science 330 (6000), 94-97, 2010
Upoważnienia: US National Institutes of Health, Howard Hughes Medical Institute
An IL-17–dominant immune profile is shared across the major orphan forms of ichthyosis
AS Paller, Y Renert-Yuval, M Suprun, H Esaki, M Oliva, TN Huynh, ...
Journal of Allergy and Clinical Immunology 139 (1), 152-165, 2017
Upoważnienia: US National Institutes of Health
Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia
YH Lim, D Ovejero, JS Sugarman, CMC DeKlotz, A Maruri, LF Eichenfield, ...
Human molecular genetics 23 (2), 397-407, 2014
Upoważnienia: US National Institutes of Health, Doris Duke Charitable Foundation
GNA14 somatic mutation causes congenital and sporadic vascular tumors by MAPK activation
YH Lim, A Bacchiocchi, J Qiu, R Straub, A Bruckner, L Bercovitch, ...
The American Journal of Human Genetics 99 (2), 443-450, 2016
Upoważnienia: US National Institutes of Health, Doris Duke Charitable Foundation
Topical cholesterol/lovastatin for the treatment of porokeratosis: a pathogenesis-directed therapy
L Atzmony, YH Lim, C Hamilton, JS Leventhal, A Wagner, AS Paller, ...
Journal of the American Academy of Dermatology 82 (1), 123-131, 2020
Upoważnienia: US National Institutes of Health
Genotype-guided medical treatment of an arteriovenous malformation in a child
R Lekwuttikarn, YH Lim, S Admani, KA Choate, JMC Teng
JAMA dermatology 155 (2), 256-257, 2019
Upoważnienia: US National Institutes of Health
Single-cell analysis reveals a hair follicle dermal niche molecular differentiation trajectory that begins prior to morphogenesis
K Gupta, J Levinsohn, G Linderman, D Chen, TY Sun, D Dong, ...
Developmental cell 48 (1), 17-31. e6, 2019
Upoważnienia: US National Institutes of Health
CARD14-associated papulosquamous eruption: a spectrum including features of psoriasis and pityriasis rubra pilaris
BG Craiglow, LM Boyden, R Hu, M Virtanen, J Su, G Rodriguez, ...
Journal of the American Academy of Dermatology 79 (3), 487-494, 2018
Upoważnienia: US National Institutes of Health
Whole exome sequencing reveals somatic mutations in HRAS and KRAS which cause nevus sebaceus
JL Levinsohn, LC Tian, LM Boyden, JM McNiff, D Narayan, ES Loring, ...
The Journal of investigative dermatology 133 (3), 827, 2012
Upoważnienia: US National Institutes of Health, Howard Hughes Medical Institute, Doris …
Mutations in KDSR cause recessive progressive symmetric erythrokeratoderma
LM Boyden, NG Vincent, J Zhou, R Hu, BG Craiglow, SJ Bayliss, ...
The American Journal of Human Genetics 100 (6), 978-984, 2017
Upoważnienia: US National Institutes of Health, Doris Duke Charitable Foundation
Somatic activating RAS mutations cause vascular tumors including pyogenic granuloma
YH Lim, SR Douglas, CJ Ko, RJ Antaya, JM McNiff, J Zhou, KA Choate, ...
The Journal of investigative dermatology 135 (6), 1698, 2015
Upoważnienia: US National Institutes of Health, Doris Duke Charitable Foundation
Second-hit, postzygotic PMVK and MVD mutations in linear porokeratosis
L Atzmony, HM Khan, YH Lim, AS Paller, JL Levinsohn, KE Holland, ...
JAMA dermatology 155 (5), 548-555, 2019
Upoważnienia: US National Institutes of Health
Frequent somatic reversion of KRT1 mutations in ichthyosis with confetti
KA Choate, Y Lu, J Zhou, PM Elias, S Zaidi, AS Paller, A Farhi, ...
The Journal of clinical investigation 125 (4), 1703-1707, 2015
Upoważnienia: US National Institutes of Health, Howard Hughes Medical Institute, Doris …
Dominant de novo mutations in GJA1 cause erythrokeratodermia variabilis et progressiva, without features of oculodentodigital dysplasia
LM Boyden, BG Craiglow, J Zhou, R Hu, EC Loring, KD Morel, CT Lauren, ...
The Journal of investigative dermatology 135 (6), 1540, 2014
Upoważnienia: US National Institutes of Health, Doris Duke Charitable Foundation
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