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Longer titles found: Malignant infantile osteopetrosis (view)

searching for Osteopetrosis 21 found (84 total)

alternate case: osteopetrosis

OSTM1 (842 words) [view diff] exact match in snippet view article find links to article

Osteopetrosis-associated transmembrane protein 1 is a protein that in humans is encoded by the OSTM1 gene. It is required for osteoclast and melanocyte
RANK (3,047 words) [view diff] exact match in snippet view article find links to article
Mutations affecting RANK have been associated with infantile malignant osteopetrosis in humans, mice and cats. RANK is a 616 amino acid type I transmembrane
Sandwich vertebra (151 words) [view diff] exact match in snippet view article find links to article
|title= (help) Kirkland, Jared D.; O’Brien, William T (August 2015). "Osteopetrosis – Classic Imaging Findings in the Spine". Journal of Clinical and Diagnostic
Sorting nexin 10 (493 words) [view diff] exact match in snippet view article find links to article
Bar-Shavit Z, Elpeleg O (2012). "An SNX10 mutation causes malignant osteopetrosis of infancy". J. Med. Genet. 49 (4): 221–6. doi:10.1136/jmedgenet-2011-100520
Hydrogen potassium ATPase (2,338 words) [view diff] exact match in snippet view article find links to article
down regulation of alpha3 subunit increasing damage to astrocytes. Osteopetrosis via TCIRG1 gene has a strong association with pre-senile dementia. Discovery
Leucosis (146 words) [view diff] exact match in snippet view article find links to article
diseases Avian sarcoma leukosis virus Lymphoid leucosis Erythroblastosis Osteopetrosis Myeloblastose Myelocytomatosis Mahy, Brian W.J. (2009). "Bovine leukemia
Pycnodysostosis (739 words) [view diff] exact match in snippet view article find links to article
Osteochondrodysplasia that has material basis in a mutation in the CTSK gene which results in dwarfism, brittle bones, osteopetrosis, shortening of the distal phalanges
Sclerosteosis (306 words) [view diff] exact match in snippet view article find links to article
doi:10.1093/hmg/10.5.537. PMID 11181578. Truswell AS (May 1958). "Osteopetrosis with syndactyly; a morphological variant of Albers-Schönberg's disease"
Macrocephaly (1,407 words) [view diff] exact match in snippet view article find links to article
Kniest dysplasia Lenz–Majewski syndrome Osteogenesis imperfecta III Osteopetrosis, autosomal recessive form Schneckenbecken dysplasia Sclerosteosis Short
Anion exchange protein 2 (1,198 words) [view diff] exact match in snippet view article find links to article
2009). "Targeted disruption of the Cl−/HCO3− exchanger Ae2 results in osteopetrosis in mice". Proc. Natl. Acad. Sci. U.S.A. 106 (5): 1638–41. doi:10.1073/pnas
Red Brangus (2,339 words) [view diff] exact match in snippet view article find links to article
species. These include, but are not limited to; syndactylism, osteopetrosis, osteopetrosis with gingival hamartomas, arachnomelia, proportionate dwarfism
List of OMIM disorder codes (18,861 words) [view diff] exact match in snippet view article find links to article
sclerosis; 300373; FAM123B Osteopetrosis, AD type I; 607634; LRP5 Osteopetrosis, autosomal dominant 2; 166600; CLCN7 Osteopetrosis, autosomal recessive 2;
Don Brothwell (1,410 words) [view diff] exact match in snippet view article find links to article
osteology in archaeology and forensic science 2002. "Ancient avian osteopetrosis: the current state of knowledge. Proceedings of the 4th Meeting of the
LRP5 (3,182 words) [view diff] exact match in snippet view article find links to article
W (Jun 2002). "Localization of the gene causing autosomal dominant osteopetrosis type I to chromosome 11q12-13". Journal of Bone and Mineral Research
Lactate dehydrogenase b (622 words) [view diff] exact match in snippet view article find links to article
distinguish Albers-Schönberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disorders". J. Bone Miner. Res. 25 (11):
Batten disease (2,748 words) [view diff] exact match in snippet view article find links to article
which is a lysosomal protein which a variety of functions. Infantile osteopetrosis: CLCN7 encodes for CLCN7. The CLN3 gene is located on the short arm
Microphthalmia-associated transcription factor (4,815 words) [view diff] exact match in snippet view article find links to article
redundant of MITF. The combined loss of both genes results in severe osteopetrosis, pointing to an interaction between MITF and other members of its transcription
Osteonecrosis of the jaw (5,110 words) [view diff] exact match in snippet view article find links to article
(November 2005). "Bisphosphonate-induced exposed bone (osteonecrosis/osteopetrosis) of the jaws: risk factors, recognition, prevention, and treatment"
Deaths in September 2007 (6,330 words) [view diff] exact match in snippet view article find links to article
Bates, 96, American mountaineer. Laurel Burch, 61, American artist, osteopetrosis. Phil Frank, 64, American cartoonist, brain tumor. Bill Griffiths, 59
List of off-label promotion pharmaceutical settlements (5,524 words) [view diff] exact match in snippet view article find links to article
the FDA to treat chronic granulomatous disease and severe malignant osteopetrosis, both extremely rare illnesses which would have generated sales of only
Bioelectricity (18,115 words) [view diff] exact match in snippet view article find links to article
CAII deficiency: A novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis". Journal of Medical Genetics. 40